John B. Mulliken, MD
Co-Director, Vascular Anomalies Center; Director, Craniofacial Center
Professor of Surgery, Harvard Medical School
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John B. Mulliken, MD
Co-Director, Vascular Anomalies Center; Director, Craniofacial Center
Professor of Surgery, Harvard Medical School
Medical Services
Languages
English
Education
Undergraduate School
Princeton University
Princeton
NJ
Medical School
Columbia University, College of Physicians and Surgeons
New York
NY
Internship
Massachusetts General Hospital
Boston
MA
Residency
Surgery
Massachusetts General Hospital
Boston
MA
Residency
Plastic Surgery
Johns Hopkins Hospital
Baltimore
MD
Fellowship
Research in Medicine
Developmental Biology Laboratory, Massachusetts General Hospital
Boston
MA
Certifications
American Board of Plastic Surgery (General)
American Board of Surgery (General)
Professional History
John B. Mulliken, M.D., received his medical degree from Columbia University, College of Physicians & Surgeons. Following his surgical residency and a research fellowship at Massachusetts General Hospital, Dr. Mulliken served in the U.S. Army in Korea and at Ft. Devens, Massachusetts. After military service, Dr. Mulliken completed his residency in plastic surgery at The Johns Hopkins Hospital and returned to Boston. Dr. Mulliken is a Professor of Surgery at Harvard Medical School and Senior Associate in Surgery at Children's Hospital Boston. He is co-director of the Vascular Anomalies Center and Director of the Craniofacial Centre and the Cleft Lip and Palate Program. He also holds an appointment at Brigham and Women's Hospital. He is a Fellow of the American College of Surgeons and a diplomate of the American Board of Surgery and the American Board of Plastic Surgery. Dr. Mulliken is the co-founder and past president of the International Society for the Study of Vascular Anomalies. He received an honorary degree from Université catholique de Louvain, Brussels. In 2014 he became an honorary fellow of the Royal College of Surgeons of London. Dr. Mulliken is the author of over 544 original scientific articles; 56 chapters; and two books. His most recent textbook is Vascular Anomalies: Hemangiomas and Malformations, co-edited with P.E. Burrows and S.J. Fishman (Oxford University Press. 2013, 1100 pgs). Dr. Mulliken's major clinical interests are cleft lip/palate, vascular anomalies and craniofacial anomalies. His basic research focuses on molecular causes of craniofacial and vascular anomalies and his clinical research concentrates on long-term outcomes following cleft lip/palate repair. Dr. Mulliken developed the internationally accepted classification system for vascular anomalies, and a one-stage repair of bilateral cleft lip and nasal deformity. Dr. Mulliken is considered one of the world's foremost experts in vascular anomalies and a master in the repair of cleft lip.
Publications
R(+) propranolol decreases lipid accumulation in haemangioma-derived stem cells. View Abstract
An endothelial SOX18-mevalonate pathway axis enables repurposing of statins for infantile hemangioma. View Abstract
Once a day administration of R(+) propranolol is sufficient to block vasculogenesis in a xenograft model of infantile hemangioma. View Abstract
R(+) Propranolol decreases lipid accumulation in hemangioma-derived stem cells. View Abstract
Infantile hemangioma: the common and enigmatic vascular tumor. View Abstract
Immunohistochemical Expression of Lymphatic Endothelial Markers in Blue Rubber Bleb Nevus Syndrome. View Abstract
Elastic Chain Premaxillary Retraction Appliance Does Not Increase Inter-Canthal Dimension in Patients with Bilateral Cleft Lip and Palate. View Abstract
An endothelial SOX18-mevalonate pathway axis enables repurposing of statins for infantile hemangioma. View Abstract
Divergent growth of the transient brain compartments in fetuses with nonsyndromic isolated clefts involving the primary and secondary palate. View Abstract
Spectrum of lymphatic anomalies in patients with RASA1-related CM-AVM. View Abstract
Surgical Resection of Vulvar Labial Venous Malformations: A Single Center Experience. View Abstract
Videofluoroscopy Versus Nasopharyngoscopy of Lateral Pharyngeal Wall Movement for Assessment of Velopharyngeal Insufficiency. View Abstract
Kaposiform Lymphangiomatosis: Pathologic Aspects in 43 Patients. View Abstract
Scalp Nodules and Deformed Great Toes: Omens of Fibrodysplasia Ossificans Progressiva. View Abstract
Non-beta blocker enantiomers of propranolol and atenolol inhibit vasculogenesis in infantile hemangioma. View Abstract
Verrucous Venous Malformation-Subcutaneous Variant. View Abstract
The Unilateral Cleft Lip Nasal Deformity: Revisions within 20 Years after Primary Correction. View Abstract
Balsam of Peru: History and Utility in Plastic Surgery. View Abstract
Classification of lower extremity venous malformations and risk of knee involvement: A retrospective cohort study. View Abstract
Philtral Ridge Projection in Repaired Unilateral Cleft Lip: Three-Dimensional Anthropometry. View Abstract
Diffuse Venous Malformations of the Upper Extremity (Bockenheimer Disease): Diagnosis and Management. View Abstract
Early Features of Progressive Hemifacial Atrophy-Clinical and Imaging Findings. View Abstract
Diffuse Venous Malformations of the Upper Extremity (Bockenheimer disease): Diagnosis and Management. View Abstract
Cleft Lip and Palate in Ectodermal Dysplasia. View Abstract
Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder. View Abstract
Techniques and results of palate fistula repair following palatoplasty: a 234-case multicenter study. View Abstract
Nasolabial Revisions in Unilateral Incomplete Cleft Lip: One Surgeon's 28-Year Experience. View Abstract
Evidence for craniofacial enhancer variation underlying nonsyndromic cleft lip and palate. View Abstract
CDH1 Mutation Distribution and Type Suggests Genetic Differences between the Etiology of Orofacial Clefting and Gastric Cancer. View Abstract
Reply: Beware the Alar Base Optical Illusion in Assessment of Unilateral Cleft Lip Nasal Deformity. View Abstract
PBX-WNT-P63-IRF6 pathway in nonsyndromic cleft lip and palate. View Abstract
"Reply: Beware the alar base optical illusion in assessment of unilateral cleft lip nasal deformity." View Abstract
Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations. View Abstract
Characterization of lymphatic malformations using primary cells and tissue transcriptomes. View Abstract
Fibroadipose Vascular Anomaly in the Upper Extremity: A Distinct Entity With Characteristic Clinical, Radiological, and Histopathological Findings. View Abstract
Association of IFT88 gene variants with nonsyndromic cleft lip with or without cleft palate. View Abstract
Beware the Alar Base Optical Illusion in Assessment of Unilateral Cleft Lip Nasal Deformity. View Abstract
Retroposition of the Globe After Le Fort III Midfacial Distraction. View Abstract
Development of the Submental Nasal Appearance Scale for the Assessment of Repaired Unilateral Complete Cleft Lip: A Pilot Study. View Abstract
Knockdown of Crispld2 in zebrafish identifies a novel network for nonsyndromic cleft lip with or without cleft palate candidate genes. View Abstract
Augmentation of the Median Tubercle with Dermis-Fat Graft in Children with Repaired Cleft Lip. View Abstract
Cleft Lip and Palate in CHARGE Syndrome: Phenotypic Features That Influence Management. View Abstract
A cross-sectional survey of long-term outcomes for patients with diffuse capillary malformation with overgrowth. View Abstract
Erratum to "Craniofacial and extracraniofacial anomalies in craniofacial macrosomia: A multicenter study of 755 patients" [J Craniomaxillofac Surg vol. 45(8) (August 2017), 1302-1310]. View Abstract
Wilms tumor screening in diffuse capillary malformation with overgrowth and macrocephaly-capillary malformation: A retrospective study. View Abstract
Somatic PIK3CA mutations are present in multiple tissues of facial infiltrating lipomatosis. View Abstract
Direct Anthropometry of Repaired Bilateral Complete Cleft Lip: A Long-Term Assessment. View Abstract
Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling. View Abstract
Evidence-Based Medicine: Secondary Correction of Cleft Lip Nasal Deformity. View Abstract
Sonographic screening for Wilms tumor in children with CLOVES syndrome. View Abstract
Craniofacial and extracraniofacial anomalies in craniofacial microsomia: a multicenter study of 755 patients’ View Abstract
Longitudinal Photogrammetric Analysis of the Columellar-Labial Angle following Primary Repair of Bilateral Cleft Lip and Nasal Deformity. View Abstract
Somatic MAP2K1 Mutations Are Associated with Extracranial Arteriovenous Malformation. View Abstract
The Changing Nasolabial Dimensions following Repair of Unilateral Cleft Lip: An Anthropometric Study in Late Childhood. View Abstract
The colourful history of malachite green: from ancient Egypt to modern surgery. View Abstract
Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations. View Abstract
Three-Dimensional Analysis of Nasal Symmetry Following Primary Correction of Unilateral Cleft Lip Nasal Deformity. View Abstract
Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma. View Abstract
Novel Rigid External Distraction Device Improves Stability and Controls the Vector During Midfacial Advancement. View Abstract
Prenatal Features Predictive of Robin Sequence Identified by Fetal Magnetic Resonance Imaging. View Abstract
Anthropometric Outcomes following Fronto-Orbital Advancement for Metopic Synostosis. View Abstract
Somatic Activating Mutations in GNAQ and GNA11 Are Associated with Congenital Hemangioma. View Abstract
An Experimental Study of Particulate Bone Graft for Secondary Inlay Cranioplasty Over Scarred Dura. View Abstract
Pharyngeal Flap Is Effective Treatment for Post Maxillary Advancement Velopharyngeal Insufficiency in Patients With Repaired Cleft Lip and Palate. View Abstract
Muenke syndrome: An international multicenter natural history study. View Abstract
Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations. View Abstract
Upper Airway Length is Predictive of Obstructive Sleep Apnea in Syndromic Craniosynostosis. View Abstract
Primary Premaxillary Setback and Repair of Bilateral Complete Cleft Lip: Indications, Technique, and Outcomes. View Abstract
Clinician's Primer to ICD-10-CM Coding for Cleft Lip/Palate Care. View Abstract
Facial Infiltrating Lipomatosis Contains Somatic PIK3CA Mutations in Multiple Tissues. View Abstract
Gastrointestinal Infantile Hemangioma: Presentation and Management. View Abstract
Classification of Cleft Lip/Palate: Then and Now. View Abstract
Effectiveness of Tongue-lip Adhesion for Obstructive Sleep Apnea in Infants With Robin Sequence Measured by Polysomnography. View Abstract
Sir William Arbuthnot Lane and His Contributions to Plastic Surgery. View Abstract
Effect of infant surgical orthopedic treatment on facial growth in preadolescent children with unilateral and bilateral complete cleft lip and palate. View Abstract
Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family. View Abstract
Outcomes of cleft lip repair for internationally adopted children. View Abstract
A somatic MAP3K3 mutation is associated with verrucous venous malformation. View Abstract
Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. View Abstract
Stewart-Treves Phenomenon: Lymphangiosarcoma Arising in Lymphedematous Tissue Is not a Syndrome. View Abstract
Capillary-venous malformation in the upper limb. View Abstract
Glucose transporter 1-positive endothelial cells in infantile hemangioma exhibit features of facultative stem cells. View Abstract
Diffuse capillary malformation in association with fetal pleural effusion: report of five patients. View Abstract
Rapidly involuting congenital hemangioma with fetal involution. View Abstract
Progressive Postnatal Pansynostosis. View Abstract
An Experimental Study of Particulate Bone Graft for Secondary Inlay Cranioplasty over Scarred Dura. View Abstract
Correction of the vestibular web during primary repair of unilateral cleft lip. View Abstract
Mandibular deformity in hemifacial microsomia: a reassessment of the Pruzansky and Kaban classification. View Abstract
Anatomic Severity, Midfacial Growth, and Speech Outcomes in Van der Woude/Popliteal Pterygium Syndromes Compared to Nonsyndromic Cleft Lip/Palate. View Abstract
Propranolol targets the contractility of infantile haemangioma-derived pericytes. View Abstract
Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate. View Abstract
Common somatic alterations identified in maffucci syndrome by molecular karyotyping. View Abstract
Safety and efficacy of bleomycin sclerotherapy for microcystic lymphatic malformation. View Abstract
The Habsburg Jaw-re-examined. View Abstract
Outcomes of cleft palatal repair for internationally adopted children. View Abstract
Theodore Dunham's Discovery of an Island Flap. View Abstract
Abstract 63: expression of follicle-stimulating hormone receptor in vascular anomalies. View Abstract
Combined metopic and unilateral coronal synostoses: a phenotypic conundrum. View Abstract
Expression of follicle-stimulating hormone receptor in vascular anomalies. View Abstract
a6-Integrin is required for the adhesion and vasculogenic potential of hemangioma stem cells. View Abstract
Abstract 75: expression of follicle-stimulating hormone receptor in vascular anomalies. View Abstract
Abstract 78: An Experimental Study of Particulate Bone Graft for Secondary Inlay Cranioplasty over Scarred Dura. View Abstract
Subfascial involvement in glomuvenous malformation. View Abstract
Intramuscular capillary-type hemangioma: radiologic-pathologic correlation. View Abstract
Fibro-adipose vascular anomaly: clinical-radiologic-pathologic features of a newly delineated disorder of the extremity. View Abstract
Reflections on the mating pool for women in plastic surgery. View Abstract
PIK3CA activating mutations in facial infiltrating lipomatosis. View Abstract
The philtrum in cleft lip: review of anatomy and techniques for construction. View Abstract
Kaposiform lymphangiomatosis: a distinct aggressive lymphatic anomaly. View Abstract
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation. View Abstract
Repair of bilateral incomplete cleft lip: techniques and outcomes. View Abstract
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. View Abstract
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. View Abstract
Diffuse capillary malformation with overgrowth: a clinical subtype of vascular anomalies with hypertrophy. View Abstract
Capillary-venous malformation in the lower limb. View Abstract
Early frontofacial symmetry after correction of unilateral coronal synostosis: frontoorbital advancement vs endoscopic strip craniectomy and helmet therapy. View Abstract
Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth. View Abstract
Genotypes and phenotypes of 162 families with a glomulin mutation. View Abstract
Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease. View Abstract
Gorham-Stout disease and generalized lymphatic anomaly--clinical, radiologic, and histologic differentiation. View Abstract
Somatic uniparental isodisomy explains multifocality of glomuvenous malformations. View Abstract
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. View Abstract
Pericytes from infantile hemangioma display proangiogenic properties and dysregulated angiopoietin-1. View Abstract
Gustav Simon's band and the evolution of labial adhesion. View Abstract
E-selectin mediates stem cell adhesion and formation of blood vessels in a murine model of infantile hemangioma. View Abstract
Speech outcome after palatal repair in nonsyndromic versus syndromic Robin sequence. View Abstract
Effect of calvarial burring on resorption of onlay cranial bone graft. View Abstract
Reharvested cranial particulate bone graft ossifies inlay calvarial defects. View Abstract
Experimental Comparison of Cranial Particulate Bone Graft, rhBMP-2, and Split Cranial Bone Graft for Inlay Cranioplasty. View Abstract
Kaposiform hemangioendothelioma: atypical features and risks of Kasabach-Merritt phenomenon in 107 referrals. View Abstract
Pathogenesis of infantile hemangiomas. View Abstract
Cerebrofacial venous anomalies, sinus pericranii, ocular abnormalities and developmental delay. View Abstract
Current surgical management of bilateral cleft lip in North America. View Abstract
Expression of androgen, estrogen, progesterone, and growth hormone receptors in vascular malformations. View Abstract
Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome. View Abstract
PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes. View Abstract
Cranial particulate bone graft ossifies calvarial defects by osteogenesis. View Abstract
Validation of the GILLS score for tongue-lip adhesion in Robin sequence patients. View Abstract
Fourth-dimensional changes in nasolabial dimensions following rotation-advancement repair of unilateral cleft lip. View Abstract
Venous malformation: risk of progression during childhood and adolescence. View Abstract
Lymphatic malformation: risk of progression during childhood and adolescence. View Abstract
Facial growth in children with complete cleft of the primary palate and intact secondary palate. View Abstract
Long-term outcome of radiofrequency ablation for intraoral microcystic lymphatic malformation. View Abstract
Facial infiltrating lipomatosis: expression of angiogenic and vasculogenic factors. View Abstract
Increased endothelial progenitor cells and vasculogenic factors in higher-staged arteriovenous malformations. View Abstract
Rapamycin suppresses self-renewal and vasculogenic potential of stem cells isolated from infantile hemangioma. View Abstract
VEGFR-1 mediates endothelial differentiation and formation of blood vessels in a murine model of infantile hemangioma. View Abstract
Thickness of orbicularis oris muscle in unilateral cleft lip: before and after labial adhesion. View Abstract
Vascular anomalies in 5,621 patients: guidelines for referral. View Abstract
Predictors of velopharyngeal insufficiency after Le Fort I maxillary advancement in patients with cleft palate. View Abstract
JAGGED1 signaling regulates hemangioma stem cell-to-pericyte/vascular smooth muscle cell differentiation. View Abstract
Positioning the caudal septum during primary repair of unilateral cleft lip. View Abstract
The GILLS score: part I. Patient selection for tongue-lip adhesion in Robin sequence. View Abstract
Vascular anomalies of the male genitalia. View Abstract
Primary lymphedema: clinical features and management in 138 pediatric patients. View Abstract
Audiologic findings in Saethre-Chotzen syndrome. View Abstract
Speech outcomes following pharyngeal flap in patients with velocardiofacial syndrome. View Abstract
Exchange cranioplasty using autologous calvarial particulate bone graft effectively repairs large cranial defects. View Abstract
Differential diagnosis of lower extremity enlargement in pediatric patients referred with a diagnosis of lymphedema. View Abstract
Safety and clinical efficacy of Onyx for embolization of extracranial head and neck vascular anomalies. View Abstract
Craniofacial growth in patients with FGFR3Pro250Arg mutation after fronto-orbital advancement in infancy. View Abstract
Complex spinal-paraspinal fast-flow lesions in CLOVES syndrome: analysis of clinical and imaging findings in 6 patients. View Abstract
Evaluation of terminology for vascular anomalies in current literature. View Abstract
Genotype-phenotype analysis of the branchio-oculo-facial syndrome. View Abstract
Meningoencephalocele and other dural disruptions: complications of Le Fort III midfacial osteotomies and distraction. View Abstract
Autologous cranial particulate bone graft: an experimental study of onlay cranioplasty. View Abstract
Interparietal bone (Os Incae) in craniosynostosis. View Abstract
Folate pathway and nonsyndromic cleft lip and palate. View Abstract
Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection. View Abstract
Ethnic heterogeneity of IRF6 AP-2a binding site promoter SNP association with nonsyndromic cleft lip and palate. View Abstract
Hermann Friedberg's case report: an early description of CLOVES syndrome. View Abstract
Inlay cranioplasty: an experimental comparison of particulate graft versus bone dust. View Abstract
Meningoencephalocele: a late complication of Le Fort III midfacial advancement in a patient with Crouzon syndrome. View Abstract
Metastatic neuroblastoma mimicking infantile hemangioma. View Abstract
Targeting NF-?B in infantile hemangioma-derived stem cells reduces VEGF-A expression. View Abstract
Audiologic findings in Pfeiffer syndrome. View Abstract
Magnetic resonance imaging for detection of brain abnormalities in fetuses with cleft lip and/or cleft palate. View Abstract
Submucous cleft palate and velopharyngeal insufficiency: comparison of speech outcomes using three operative techniques by one surgeon. View Abstract
Klippel-Trenaunay syndrome and spinal arteriovenous malformations: an erroneous association. View Abstract
LUMBAR: association between cutaneous infantile hemangiomas of the lower body and regional congenital anomalies. View Abstract
Gender differences in the professional and private lives of plastic surgeons. View Abstract
CLOVES syndrome with thoracic and central phlebectasia: increased risk of pulmonary embolism. View Abstract
Nasomaxillary dermoid. View Abstract
Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate. View Abstract
Extracranial arteriovenous malformations: natural progression and recurrence after treatment. View Abstract
Corticosteroid suppression of VEGF-A in infantile hemangioma-derived stem cells. View Abstract
Infantile myofibroma or lymphatic malformation: differential diagnosis of neonatal cystic cervicofacial lesions. View Abstract
Perioperative corticosteroid reduces hospital stay after fronto-orbital advancement. View Abstract
Autologous cranial particulate bone grafting reduces the frequency of osseous defects after cranial expansion. View Abstract
Resection of amblyogenic periocular hemangiomas: indications and outcomes. View Abstract
Pharyngeal flap outcomes in nonsyndromic children with repaired cleft palate and velopharyngeal insufficiency. View Abstract
A novel association between RASA1 mutations and spinal arteriovenous anomalies. View Abstract
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects. View Abstract
Effect of a syndromic diagnosis on mandibular size and sagittal position in Robin sequence. View Abstract
Repair of bilateral cleft lip and its variants. View Abstract
Cleft palate in Pfeiffer syndrome. View Abstract
Congenital disseminated pyogenic granuloma. View Abstract
Adult-onset kaposiform hemangioendothelioma in a posttraumatic site. View Abstract
Zygomaticotemporal suture synostosis causes progressive facial deformity and asymmetry. View Abstract
Fifty years of the Millard rotation-advancement: looking back and moving forward. View Abstract
Treatment of unilateral coronal synostosis by endoscopic strip craniectomy or fronto-orbital advancement: Ophthalmologic findings. View Abstract
Recessive primary congenital lymphoedema caused by a VEGFR3 mutation. View Abstract
Remembering Dr Judah Folkman. View Abstract
Pharmacological treatment of a diffuse arteriovenous malformation of the upper extremity in a child. View Abstract
Sense of wonder. View Abstract
Discussion. Nasoalveolar molding improves long-term nasal symmetry in complete unilateral cleft lip-cleft palate patients. View Abstract
Lesser forms of cleft lip associated with the branchio-oculo-facial syndrome. View Abstract
Increased prevalence of left-handedness in hemifacial microsomia. View Abstract
Sturge-Weber syndrome: soft-tissue and skeletal overgrowth. View Abstract
Palatoplasty outcomes in nonsyndromic patients with cleft palate: a 29-year assessment of one surgeon's experience. View Abstract
Humoral immune deficiency and hemifacial microsomia seen in one family. View Abstract
Infantile hemangiomas involving the neuraxis: clinical and imaging findings. View Abstract
The role of congenital muscular torticollis in the development of deformational plagiocephaly. View Abstract
Vascular lesions of bone in children, adolescents, and young adults. A clinicopathologic reappraisal and application of the ISSVA classification. View Abstract
Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations. View Abstract
Effect of midfacial distraction on the obstructed airway in patients with syndromic bilateral coronal synostosis. View Abstract
Minor-form, microform, and mini-microform cleft lip: anatomical features, operative techniques, and revisions. View Abstract
Asymmetrical bilateral cleft lip: complete or incomplete and contralateral lesser defect (minor-form, microform, or mini-microform). View Abstract
The frequency of palatal anomalies in Saethre-Chotzen syndrome. View Abstract
Increased frequency of left-handedness in patients with unilateral coronal synostosis. View Abstract
Simultaneous harvesting of cancellous iliac bone for alveolar cleft closure and dermis for augmentation of median tubercle. View Abstract
Phenotypically unusual combined craniosynostoses: presentation and management. View Abstract
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate. View Abstract
Pediatric cranioplasty using particulate calvarial bone graft. View Abstract
Additional EFNB1 mutations in craniofrontonasal syndrome. View Abstract
Multipotential stem cells recapitulate human infantile hemangioma in immunodeficient mice. View Abstract
Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations. View Abstract
Ramón Castroviejo: an ophthalmologist's contributions to plastic surgery. View Abstract
Validity and reliability of craniofacial anthropometric measurement of 3D digital photogrammetric images. View Abstract
A craniofacial glossary. View Abstract
TFAP2A mutations result in branchio-oculo-facial syndrome. View Abstract
Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. View Abstract
Re: Spinal epidural hemangiomas: various types of MR imaging features with histopathologic correlation. View Abstract
Cheever's double operation: the first Le Fort I osteotomy. View Abstract
Comparison of a modifiable cranial cup versus repositioning and cervical stretching for the early correction of deformational posterior plagiocephaly. View Abstract
Subglossopalatal synechia in association with cardiac and digital anomalies. View Abstract
IGF-2 and FLT-1/VEGF-R1 mRNA levels reveal distinctions and similarities between congenital and common infantile hemangioma. View Abstract
Glucose transporter-1 protein is immunohistochemically expressed in subglottic infantile haemangioma. View Abstract
Facial asymmetry in unilateral coronal synostosis: long-term results after fronto-orbital advancement. View Abstract
Risk of vascular anomalies with Down syndrome. View Abstract
Percutaneous sclerotherapy of lymphatic malformations with doxycycline. View Abstract
Multifocal rapidly involuting congenital hemangioma: a link to chorangioma. View Abstract
Accurately renaming macrocephaly-cutis marmorata telangiectatica congenita (M-CMTC) as macrocephaly-capillary malformation (M-CM). View Abstract
Primary grafting with autologous cranial particulate bone prevents osseous defects following fronto-orbital advancement. View Abstract
Repair of transverse facial cleft in hemifacial microsomia: long-term anthropometric evaluation of commissural symmetry. View Abstract
A case of Proteus syndrome with lateral embryonal vein and frontal intraosseous lipoma. View Abstract
CRISPLD2: a novel NSCLP candidate gene. View Abstract
Reticular infantile hemangioma of the limb can be associated with ventral-caudal anomalies, refractory ulceration, and cardiac overload. View Abstract
Frequency of Le Fort I osteotomy after repaired cleft lip and palate or cleft palate. View Abstract
Astigmatism in unilateral coronal synostosis: incidence and laterality. View Abstract
The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management. View Abstract
Intraosseous "hemangiomas" are malformations and not tumors. View Abstract
Schimmelpenning syndrome: an association with vascular anomalies. View Abstract
Intracranial vascular anomalies in patients with periorbital lymphatic and lymphaticovenous malformations. View Abstract
Hepatic hemangiomas: subtype classification and development of a clinical practice algorithm and registry. View Abstract
Zygomaticotemporal synostosis: a rare cause of progressive facial asymmetry. View Abstract
Radiofrequency ablation of microcystic lymphatic malformation in the oral cavity. View Abstract
Apert syndrome: what prenatal radiographic findings should prompt its consideration? View Abstract
Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations. View Abstract
Prevention of temporal depression that follows fronto-orbital advancement for craniosynostosis. View Abstract
Hypopituitarism in PHACES Association. View Abstract
Endothelial progenitor cells from infantile hemangioma and umbilical cord blood display unique cellular responses to endostatin. View Abstract
Intracranial anomalies detected by imaging studies in 30 patients with Apert syndrome. View Abstract
Verrucous hemangioma revisited. View Abstract
Genuine diffuse phlebectasia of Bockenheimer: dissection of an eponym. View Abstract
Congenital fenestration of the palate: A case of embryologic syzygy. View Abstract
The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males. View Abstract
Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia. View Abstract
Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients. View Abstract
Mesenchymal stem cells and adipogenesis in hemangioma involution. View Abstract
Robin sequence: a retrospective review of 115 patients. View Abstract
Combined push-pull distraction for correction of syndromic midfacial hypoplasia. View Abstract
Evidence by molecular profiling for a placental origin of infantile hemangioma. View Abstract
Real-time magnetic resonance imaging aids prenatal diagnosis of isolated cleft palate. View Abstract
Double unilimb Z-plastic repair of microform cleft lip. View Abstract
D2-40 immunohistochemical analysis of pediatric vascular tumors reveals positivity in kaposiform hemangioendothelioma. View Abstract
Expression of Wilms tumor 1 gene distinguishes vascular malformations from proliferative endothelial lesions. View Abstract
Variation in IRF6 contributes to nonsyndromic cleft lip and palate. View Abstract
Management of parotid hemangioma. View Abstract
Cutaneovisceral angiomatosis with thrombocytopenia. View Abstract
Iliac artery stenosis in a child with cutis marmorata telangiectatica congenita. View Abstract
Frontonasal osteotomy to facilitate removal of an intracranial nasal dermoid. View Abstract
Increased expression of urinary matrix metalloproteinases parallels the extent and activity of vascular anomalies. View Abstract
Vascular tumors of the heart in infants and children: case series and review of the literature. View Abstract
Involvement of the basilar coronal ring in unilateral coronal synostosis. View Abstract
Lymphatic malformation of the lingual base and oral floor. View Abstract
RASA1: variable phenotype with capillary and arteriovenous malformations. View Abstract
Concordant contralateral lambdoidal synostosis in dizygotic twins. View Abstract
Auricular arteriovenous malformation: evaluation, management, and outcome. View Abstract
Kaposiform hemangioendothelioma without Kasabach-Merritt phenomenon. View Abstract
Blue rubber bleb nevus syndrome: surgical eradication of gastrointestinal bleeding. View Abstract
An association between hemifacial microsomia and facial clefting. View Abstract
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect. View Abstract
Heterotopic neural nodules of the scalp. View Abstract
Periorbital lymphatic malformation: clinical course and management in 42 patients. View Abstract
Current management of hemangiomas and vascular malformations. View Abstract
The molders of this plastic surgeon and his quest for symmetry. View Abstract
Description of a case of distal 2p trisomy by array-based comparative genomic hybridization: a high resolution genome-wide investigation for chromosomal aneuploidy in a single assay. View Abstract
Demographic and reproductive factors associated with hemifacial microsomia. View Abstract
The changing faces of children with cleft lip and palate. View Abstract
Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities. View Abstract
Genomic imprinting of IGF2 is maintained in infantile hemangioma despite its high level of expression. View Abstract
Prenatal diagnosis of cleft lip and cleft palate using MRI. View Abstract
Unilateral coronal synostosis: a histomorphometric study. View Abstract
Molecular analysis of patients with synostotic frontal plagiocephaly (unilateral coronal synostosis). View Abstract
Vasoactive exposures, vascular events, and hemifacial microsomia. View Abstract
Congenital hemangiomas and infantile hemangioma: missing links. View Abstract
Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 13-2004. A newborn girl with a large cutaneous lesion, thrombocytopenia, and anemia. View Abstract
Bilateral cleft lip. View Abstract
Wilms tumor screening is unnecessary in Klippel-Trenaunay syndrome. View Abstract
Association of chromosomal regions 3p21.2, 10p13, and 16p13.3 with nonsyndromic cleft lip and palate. View Abstract
Nonsyndromic cleft lip and palate: four chromosomal regions of interest. View Abstract
Management of parotid hemangioma in 100 children. View Abstract
Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations. View Abstract
Partial oral duplication: a defect in ectomesenchymal migration? View Abstract
Rapidly involuting congenital hemangioma: clinical and histopathologic features. View Abstract
Endothelial progenitor cells in infantile hemangioma. View Abstract
Differential expression of CD146 in tissues and endothelial cells derived from infantile haemangioma and normal human skin. View Abstract
Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening. View Abstract
The effects of active infant orthopedics on occlusal relationships in unilateral complete cleft lip and palate. View Abstract
Anthropometric study of synostotic frontal plagiocephaly: before and after fronto-orbital advancement with correction of nasal angulation. View Abstract
Repair of bilateral cleft lip: review, revisions, and reflections. View Abstract
Effects of a child with a craniofacial anomaly on stability of the parental relationship. View Abstract
Complications associated with cleft lip and palate repair. View Abstract
The presentation and management of nasal dermoid: a 30-year experience. View Abstract
Binderoid complete cleft lip/palate. View Abstract
Professor Edmund Rose: his position in surgery. View Abstract
Venous malformations of skeletal muscle. View Abstract
Incidence of cranial asymmetry in healthy newborns. View Abstract
Diprosopus: a unique case and review of the literature. View Abstract
Fast-flow lingual vascular anomalies in the young patient: is imaging diagnostic? View Abstract
A sense of wonder. View Abstract
Cervicofacial venous malformations. MRI features and interventional strategies. View Abstract
Unilateral fusion of the frontosphenoidal suture: a rare cause of synostotic frontal plagiocephaly. View Abstract
Three-dimensional prenatal diagnosis of frontonasal malformation and unilateral cleft lip/palate. View Abstract
Resorbable internal splint: an adjunct to primary correction of unilateral cleft lip-nasal deformity. View Abstract
Anthropometric analysis of mandibular asymmetry in infants with deformational posterior plagiocephaly. View Abstract
MTHFR is not a risk factor in the development of isolated nonsyndromic cleft lip and palate. View Abstract
Evidence for a cleft palate only locus on chromosome 4 near MSX1. View Abstract
Angiographic features of rapidly involuting congenital hemangioma (RICH). View Abstract
Locus for susceptibility for familial capillary malformation ('port-wine stain') maps to 5q. View Abstract
Circular excision of hemangioma and purse-string closure: the smallest possible scar. View Abstract
Prenatal diagnosis of vascular anomalies. View Abstract
Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas"). View Abstract
Successful antiangiogenic therapy of giant cell angioblastoma with interferon alfa 2b: report of 2 cases. View Abstract
The craniofacial surgeon as amateur geneticist. View Abstract
Increased Tie2 expression, enhanced response to angiopoietin-1, and dysregulated angiopoietin-2 expression in hemangioma-derived endothelial cells. View Abstract
Prenatal diagnosis of cleft lip: what the sonologist needs to tell the surgeon. View Abstract
Facial infiltrating lipomatosis. View Abstract
Vascular anomalies: classification, diagnosis, and natural history. View Abstract
Prenatal sonographic diagnosis of major craniofacial anomalies. View Abstract
Molecular genetics of vascular malformations. View Abstract
Facial "glomangiomas": large facial venous malformations with glomus cells. View Abstract
Townes-Brocks syndrome versus expanded spectrum hemifacial microsomia: review of eight patients and further evidence of a "hot spot" for mutation in the SALL1 gene. View Abstract
Primary repair of bilateral cleft lip and nasal deformity. View Abstract
Noninvoluting congenital hemangioma: a rare cutaneous vascular anomaly. View Abstract
Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK. View Abstract
Clonality and altered behavior of endothelial cells from hemangiomas. View Abstract
Craniofacial, temporal bone, and audiologic abnormalities in the spectrum of hemifacial microsomia. View Abstract
Repair of bilateral complete cleft lip: intraoperative nasolabial anthropometry. View Abstract
Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YAC. View Abstract
Hypodontia in hemifacial microsomia. View Abstract
Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnoses. View Abstract
Tc-99m red blood cell imaging of blue rubber bleb nevus syndrome. View Abstract
Vascular anomalies. View Abstract
Repair of bilateral complete cleft lip and nasal deformity--state of the art. View Abstract
Cross-cultural understanding of aesthetic surgery: the male cosmetic surgery patient in japan and the USA. View Abstract
No evidence supporting MTHFR as a risk factor in the development of familial NSCLP. View Abstract
VEGF and its receptors are expressed in a pediatric angiosarcoma in a patient with Aicardi's syndrome. View Abstract
Analysis of fronto-orbital advancement for Apert, Crouzon, Pfeiffer, and Saethre-Chotzen syndromes. View Abstract
KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation. View Abstract
Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis. View Abstract
Soft-tissue vascular anomalies: utility of US for diagnosis. View Abstract
Residual lesions after Kasabach-Merritt phenomenon in 41 patients. View Abstract
Progression of facial asymmetry in hemifacial microsomia. View Abstract
Nonsyndromic cleft lip and palate is not associated with cancer or other birth defects. View Abstract
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia. View Abstract
Molecular diagnosis of bilateral coronal synostosis. View Abstract
Complications of systemic corticosteroid therapy for problematic hemangioma. View Abstract
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes. View Abstract
The principle of rotation advancement for repair of unilateral complete cleft lip and nasal deformity: technical variations and analysis of results. View Abstract
Children with repaired bilateral cleft lip/palate: effect of age at premaxillary osteotomy on facial growth. View Abstract
Vascular malformations of the upper limb: a review of 270 patients. View Abstract
Prelaminated free flap reconstruction of complex central facial defects. View Abstract
The infant with a vascular tumor. View Abstract
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22. View Abstract
Sclerotherapy of craniofacial venous malformations: complications and results. View Abstract
Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation. View Abstract
Antiangiogenic therapy of a recurrent giant cell tumor of the mandible with interferon alfa-2a. View Abstract
The role of matrix metalloproteinase activity in the maturation of human capillary endothelial cells in vitro. View Abstract
Prospective anthropometric analysis of sagittal orbital-globe relationship following fronto-orbital advancement in childhood. View Abstract
Progressive growth of infantile cutaneous hemangiomas is directly correlated with hyperplasia and angiogenesis of adjacent epidermis and inversely correlated with expression of the endogenous angiogenesis inhibitor, IFN-beta. View Abstract
A new syndrome: heart defects, laryngeal anomalies, preaxial polydactyly, and colonic aganglionosis in sibs. View Abstract
Simultaneous maxillary and mandibular distraction osteogenesis with a semiburied device. View Abstract
Analysis of posterior plagiocephaly: deformational versus synostotic. View Abstract
Human NELL-1 expressed in unilateral coronal synostosis. View Abstract
Hemifacial microsomia: anatomical prediction of difficult intubation. View Abstract
Vascular anomalies. A primer for pediatricians. View Abstract
Transnasal endoscopic excision of midline nasal dermoid from the anterior cranial base. View Abstract
Photogrammetric comparison of two methods for synchronous repair of bilateral cleft lip and nasal deformity. View Abstract
Molecular basis of vascular anomalies. View Abstract
Arteriovenous malformations of the head and neck: natural history and management. View Abstract
Möbius syndrome: classification and grading system. View Abstract
Gastrointestinal manifestations of vascular anomalies in childhood: varied etiologies require multiple therapeutic modalities. View Abstract
New instrument for orbital anthropometry. View Abstract
Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations. View Abstract
Cerebral vasculopathy and neurologic sequelae in infants with cervicofacial hemangioma: report of eight patients. View Abstract
Surgical correction of mandibular hypoplasia in hemifacial microsomia: the case for treatment in early childhood. View Abstract
Polyethylene glycol/microfibrillar collagen composite as a new resorbable hemostatic bone wax. View Abstract
Velopharyngeal function in nonsyndromic cleft palate: relevance of surgical technique, age at repair, and cleft type. View Abstract
Spastic diplegia as a complication of interferon Alfa-2a treatment of hemangiomas of infancy. View Abstract
Midfacial growth after costochondral graft construction of the mandibular ramus in hemifacial microsomia. View Abstract
The mutations in FGFR2-associated craniosynostoses are clustered in five structural elements of immunoglobulin-like domain III of the receptor. View Abstract
Four cases of mucosal neuroma syndrome: multiple endocrine neoplasm 2B or not 2B? View Abstract
Cleft lip with or without cleft palate: effect of family history on reproductive planning, surgical timing, and parental stress. View Abstract
Increased apoptosis coincides with onset of involution in infantile hemangioma. View Abstract
Thrombocytopenic coagulopathy (Kasabach-Merritt phenomenon) is associated with Kaposiform hemangioendothelioma and not with common infantile hemangioma. View Abstract
Synostotic frontal plagiocephaly: anthropometric comparison of three techniques for surgical correction. View Abstract
Effect of lip adhesion on labial height in two-stage repair of unilateral complete cleft lip. View Abstract
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. View Abstract
Robin sequence: obstructive sleep apnea following pharyngeal flap. View Abstract
Tissue expansion in children: a retrospective study of complications. View Abstract
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. View Abstract
Molding therapy for infants with deformational auricular anomalies. View Abstract
Hemangioma in twins. View Abstract
Hypertelorism: nosologic analysis of 90 patients. View Abstract
Vascular tumors and vascular malformations (new issues). View Abstract
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2. View Abstract
Jugular foraminal stenosis in Crouzon syndrome. View Abstract
Abnormalities of the cranial base in synostotic frontal plagiocephaly. View Abstract
Hepatic vascular anomalies in infancy: a twenty-seven-year experience. View Abstract
Nonsyndromic cleft lip with or without cleft palate: erratum. View Abstract
Langerhans cell histiocytosis: an uncommon disease commonly manifesting in the craniofacial skeleton. View Abstract
Cranial plate and screw fixation in infancy: an assessment of risk. View Abstract
Vascular cutaneous anomalies in children: malformations and hemangiomas. View Abstract
The concept of the sagittal orbital-globe relationship in craniofacial surgery. View Abstract
E-selectin is present in proliferating endothelial cells in human hemangiomas. View Abstract
Congenital hemangioma: evidence of accelerated involution. View Abstract
Molecular genetics and craniofacial surgery. View Abstract
Treacher Collins syndrome: phenotypic variability in a family including an infant with arhinia and uveal colobomas. View Abstract
Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene. View Abstract
Exclusion of linkage between cleft lip with or without cleft palate and markers on chromosomes 4 and 6. View Abstract
Large nasal tip teratoma. View Abstract
Congenital fibrosarcoma masquerading as congenital hemangioma: report of two cases. View Abstract
OMENS-Plus: analysis of craniofacial and extracraniofacial anomalies in hemifacial microsomia. View Abstract
Additional corrections: interferon for hemangiomas of infancy. View Abstract
Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. View Abstract
Bilateral complete cleft lip and nasal deformity: an anthropometric analysis of staged to synchronous repair. View Abstract
Predisposition for cysteine substitutions in the immunoglobulin-like chain of FGFR2 in Crouzon syndrome. View Abstract
Cervicofacial lymphatic malformation: clinical course, surgical intervention, and pathogenesis of skeletal hypertrophy. View Abstract
Retention of a composite dressing for alveolopalatal wounds. View Abstract
A gene for familial venous malformations maps to chromosome 9p in a second large kindred. View Abstract
Not all hemangiomas look like strawberries: uncommon presentations of the most common tumor of infancy. View Abstract
Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family. View Abstract
Congenital fibrosarcoma masquerading as lymphatic malformation: report of two cases. View Abstract
Frontal plagiocephaly. Diagnosis and treatment. View Abstract
Assignment of a locus for dominantly inherited venous malformations to chromosome 9p. View Abstract
Marked female predilection in some syndromes associated with facial hemangiomas. View Abstract
Cellular markers that distinguish the phases of hemangioma during infancy and childhood. View Abstract
Three-dimensional folded free-flap reconstruction of complex facial defects using intraoperative modeling. View Abstract
Hemangiomas and vascular malformations of the head and neck: MR characterization. View Abstract
Hemangiomas and vascular malformations of infancy and childhood. View Abstract
Association between "plagiocephaly" and hemifacial microsomia. View Abstract
The current management of vascular birthmarks. View Abstract
Cutaneous vascular anomalies. View Abstract
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. View Abstract
Fetal cleft lip and palate: sonographic diagnosis and postnatal outcome. View Abstract
The anatomy of Cupid's bow in normal and cleft lip. View Abstract
Computer-assisted three-dimensional planning in craniofacial surgery. View Abstract
Newly recognized autosomal dominant disorder with craniosynostosis. View Abstract
Enophthalmos following orbital transposition for craniofacial malformations. View Abstract
Ocular manifestations of deformational frontal plagiocephaly. View Abstract
Assignment of a gene locus involved in craniosynostosis to chromosome 5qter. View Abstract
Isolation and characterization of human heparin. View Abstract
The use of scapular and parascapular flaps for cheek reconstruction. View Abstract
A biologic approach to cutaneous vascular anomalies. View Abstract
Correction of the bilateral cleft lip nasal deformity: evolution of a surgical concept. View Abstract
Interferon alfa-2a therapy for life-threatening hemangiomas of infancy. View Abstract
Treatment options for periorbital hemangioma of infancy. View Abstract
Frontal plagiocephaly: synostotic, compensational, or deformational. View Abstract
Pyogenic granuloma (lobular capillary hemangioma): a clinicopathologic study of 178 cases. View Abstract
Is there an association between hemangioma and syndromes with dysmorphic features? View Abstract
Interferon alpha therapy of haemangiomas in newborns and infants. View Abstract
Biological classification of soft-tissue vascular anomalies: MR correlation. View Abstract
Neurosurgical complications in craniofacial surgery. View Abstract
Surgical correction of the craniofacial anomalies in Apert syndrome. View Abstract
A plea for a biologic approach to hemangiomas of infancy. View Abstract
Craniofacial anomalies in twins. View Abstract
The O.M.E.N.S. classification of hemifacial microsomia. View Abstract
Calvarial sutural abnormalities: metopic synostosis and coronal deformation--an anatomic, three-dimensional radiographic, and pathologic study. View Abstract
The healing of bone and cartilage. View Abstract
Clinical and ultrastructural studies of Romberg's hemifacial atrophy. View Abstract
A retrospective analysis of growth of the constructed condyle-ramus in children with hemifacial microsomia. View Abstract
Deepithelialized mucosal-submucosal flaps to correct the "whistling lip" deformity. View Abstract
Ocular dermoids. View Abstract
The cleft lip lower-lip deformity. View Abstract
Venous air embolism during a craniofacial procedure. View Abstract
Surgical correction of hemifacial microsomia in the growing child. View Abstract
Correction of cryptotia using tissue expansion. View Abstract
Surgical division of craniopagi. View Abstract
Fragmented care of facial fractures. View Abstract
Midfacial duplication: a rare malformation sequence. View Abstract
Analysis and treatment of hemifacial microsomia in childhood. View Abstract
Macroglossia: a review of the condition and a new classification. View Abstract
Midface position after Le Fort III advancement: a long-term follow-up study. View Abstract
Correction of hemifacial microsomia in the growing child: a follow-up study. View Abstract
Vascular anomalies of the maxillofacial region. View Abstract
Facial skeletal changes following hypertelorbitism correction. View Abstract
An ultrastructural study of mast cell interactions in hemangiomas. View Abstract
Microtia: a microform of hemifacial microsomia. View Abstract
Classification and rationale for management of vascular anomalies in the upper extremity. View Abstract
Antibiotic prophylaxis for major maxillocraniofacial surgery. View Abstract
Midline cervical cleft. View Abstract
Principles and techniques of bilateral complete cleft lip repair. View Abstract
Demineralized bone implants. View Abstract
Skeletal changes associated with vascular malformations. View Abstract
Induced osteogenesis--the biological principle and clinical applications. View Abstract
Analysis and treatment of hemifacial microsomia. View Abstract
Donor-site morbidity after harvesting rib and iliac bone. View Abstract
The use of demineralized xenogeneic bone implants to correct phalangeal defects: a case report. View Abstract
Midface position after LeFort III advancement. View Abstract
Congenital vascular lesions: clinical application of a new classification. View Abstract
Childhood hemangiomas and vascular malformations: angiographic differentiation. View Abstract
Microanalysis of epithelial and mesenchymal acid hydrolase activities in the developing palate. View Abstract
Treatment of jaw defects with demineralized bone implants. View Abstract
The evolution of techniques for reconstruction of full-thickness cheek defects. View Abstract
In vitro characteristics of endothelium from hemangiomas and vascular malformations. View Abstract
Mast cells in hemangiomas and vascular malformations. View Abstract
Classification of pediatric vascular lesions. View Abstract
A method for treating severe burn contractures of the tendoachilles in children. View Abstract
Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics. View Abstract
Bone implants and induced osteogenesis. View Abstract
Correction of anteriorly displaced medial canthus by tendon retropositioning. View Abstract
Use of demineralized allogeneic bone implants for the correction of maxillocraniofacial deformities. View Abstract
Application of the biological principle of induced osteogenesis for craniofacial defects. View Abstract
Three-dimensional approach to analysis and treatment of hemifacial microsomia. View Abstract
Fate of mineralized and demineralized osseous implants in cranial defects. View Abstract
A microangiographic study of hematoma-associated flap necrosis and salvage with isoxsuprine. View Abstract
Restoration of facial contour using free vascularized omental transfer. View Abstract
Induced osteogenesis for repair and construction in the craniofacial region. View Abstract
Povidone-iodine and tensile strength of wounds in rats. View Abstract
Thumb lengthening by metacarpal distraction. View Abstract
Twenty year experience in maxillocraniofacial surgery. An evaluation of early surgery on growth, function and body image. View Abstract
Pathogenesis of skin flap necrosis from an underlying hematoma. View Abstract
Major intravenous extravasation injuries. View Abstract
Pathogenesis of skin flap necrosis from an underlying hematoma. View Abstract
Cosmetic surgery as an antecedent of life change. View Abstract
Impressions of Charles Stent. View Abstract
Sialadenitis in childhood. View Abstract
Management of a vascular malformation of the face using total circulatory arrest. View Abstract
General plastic surgical principles. View Abstract
Management of facial fractures in children. View Abstract
Biographical sketch of Charles Conrad Miller, "featural surgeon". View Abstract
An experimental study of hematoma and flap necrosis. View Abstract
Dermabrasion and limited excision of the fibrous papules of tuberous sclerosis: case report. View Abstract
Facial fractures in children: an analysis of 122 fractures in 109 patients. View Abstract
Vaccination caveat. The off-the-shoulder look. View Abstract
Effects of intralesional injection of triamcinolone on glucose-6-phosphate dehydrogenase and alanine aminotransferase activity in keloids. View Abstract
The selection of antibiotics for human bites of the hand. View Abstract
Location of the levator veli palatini insertion following levator retropositioning, palatal pushback, and pharyngeal flap procedures. View Abstract
Samuel Prescott: physician-patriot. View Abstract
W-epicanthoplasty. View Abstract
A large frontoethmoidal encephalomeningocele. Case report. View Abstract
Charles Augustus Leale: Lincol's young physician. View Abstract
Small bowel obstruction secondary to atheromatous embolism. A case report and review of the literature. View Abstract
The limits of tracheal resection with primary anastomosis: further anatomical studies in man. View Abstract
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