Published in Skeletal Radiol on January 31, 2013
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Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations. Nat Genet (2008) 1.95
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. Nat Genet (2013) 1.82
Variation in IRF6 contributes to nonsyndromic cleft lip and palate. Am J Med Genet A (2005) 1.82
TFAP2A mutations result in branchio-oculo-facial syndrome. Am J Hum Genet (2008) 1.79
Kaposiform hemangioendothelioma without Kasabach-Merritt phenomenon. J Am Acad Dermatol (2005) 1.77
The effect of hospital volume of pediatric appendectomies on the misdiagnosis of appendicitis in children. Pediatrics (2004) 1.76
Rapamycin suppresses self-renewal and vasculogenic potential of stem cells isolated from infantile hemangioma. J Invest Dermatol (2011) 1.74
Effects of race, insurance status, and hospital volume on perforated appendicitis in children. Pediatrics (2005) 1.73
Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities. Arch Dermatol (2004) 1.73
Increased expression of urinary matrix metalloproteinases parallels the extent and activity of vascular anomalies. Pediatrics (2005) 1.72
Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas"). Am J Hum Genet (2002) 1.66
Resection of amblyogenic periocular hemangiomas: indications and outcomes. Plast Reconstr Surg (2010) 1.65
The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management. J Med Genet (2007) 1.64
Kaposiform hemangioendothelioma: atypical features and risks of Kasabach-Merritt phenomenon in 107 referrals. J Pediatr (2012) 1.63
Extracranial arteriovenous malformations: natural progression and recurrence after treatment. Plast Reconstr Surg (2010) 1.61
Blue rubber bleb nevus syndrome: surgical eradication of gastrointestinal bleeding. Ann Surg (2005) 1.59
Neonatal thoracoscopic repair of congenital diaphragmatic hernia: selection criteria for successful outcome. J Pediatr Surg (2005) 1.57
Involvement of the basilar coronal ring in unilateral coronal synostosis. Plast Reconstr Surg (2005) 1.52
Endothelial progenitor cells in infantile hemangioma. Blood (2003) 1.50
Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease. Am J Med Genet A (2013) 1.46
Robin sequence: a retrospective review of 115 patients. Int J Pediatr Otorhinolaryngol (2006) 1.45
Current surgical management of bilateral cleft lip in North America. Plast Reconstr Surg (2012) 1.44
Hepatic hemangiomas: subtype classification and development of a clinical practice algorithm and registry. J Pediatr Surg (2007) 1.43
Speech outcomes following pharyngeal flap in patients with velocardiofacial syndrome. Plast Reconstr Surg (2011) 1.42
Endothelial progenitor cells from infantile hemangioma and umbilical cord blood display unique cellular responses to endostatin. Blood (2006) 1.40
The Changing Nasolabial Dimensions following Repair of Unilateral Cleft Lip: An Anthropometric Study in Late Childhood. Plast Reconstr Surg (2016) 1.40
Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. Hum Mol Genet (2008) 1.39
Newborn and toddler intestinal obstruction owing to congenital mesenteric defects. J Pediatr Surg (2008) 1.38
Primary lymphedema: clinical features and management in 138 pediatric patients. Plast Reconstr Surg (2011) 1.38
Infantile hepatic hemangiomas: clinical and imaging findings and their correlation with therapy. AJR Am J Roentgenol (2004) 1.36
Differential expression of CD146 in tissues and endothelial cells derived from infantile haemangioma and normal human skin. J Pathol (2003) 1.35
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome. PLoS Genet (2011) 1.34
CRISPLD2: a novel NSCLP candidate gene. Hum Mol Genet (2007) 1.32
Rapidly involuting congenital hemangioma: clinical and histopathologic features. Pediatr Dev Pathol (2004) 1.32
Evidence by molecular profiling for a placental origin of infantile hemangioma. Proc Natl Acad Sci U S A (2005) 1.28
Mesenchymal stem cells and adipogenesis in hemangioma involution. Stem Cells (2006) 1.25
IGF-2 and FLT-1/VEGF-R1 mRNA levels reveal distinctions and similarities between congenital and common infantile hemangioma. Pediatr Res (2008) 1.25
Management of parotid hemangioma in 100 children. Plast Reconstr Surg (2004) 1.24
Verrucous hemangioma revisited. Pediatr Dermatol (2006) 1.22
The presentation and management of nasal dermoid: a 30-year experience. Arch Otolaryngol Head Neck Surg (2003) 1.22
Esophageal atresia, duodenal atresia, and unilateral lung agenesis: a case report. J Pediatr Surg (2004) 1.22
The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males. Am J Hum Genet (2006) 1.22
Vascular lesions of bone in children, adolescents, and young adults. A clinicopathologic reappraisal and application of the ISSVA classification. Virchows Arch (2008) 1.22
Childhood asymmetric labium majus enlargement: mimicking a neoplasm. Am J Surg Pathol (2005) 1.19
Diffuse capillary malformation with overgrowth: a clinical subtype of vascular anomalies with hypertrophy. J Am Acad Dermatol (2013) 1.19
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects. Eur J Hum Genet (2009) 1.17
Balanitis xerotica obliterans in boys. J Urol (2005) 1.16
Evaluation of terminology for vascular anomalies in current literature. Plast Reconstr Surg (2011) 1.15
Percutaneous sclerotherapy of lymphatic malformations with doxycycline. Lymphat Res Biol (2008) 1.14
Resorbable internal splint: an adjunct to primary correction of unilateral cleft lip-nasal deformity. Plast Reconstr Surg (2002) 1.12
Successful antiangiogenic therapy of giant cell angioblastoma with interferon alfa 2b: report of 2 cases. Pediatrics (2002) 1.12
Identification of signaling systems in proliferating and involuting phase infantile hemangiomas by genome-wide transcriptional profiling. Am J Pathol (2009) 1.11
CLOVES syndrome with thoracic and central phlebectasia: increased risk of pulmonary embolism. J Thorac Cardiovasc Surg (2010) 1.11
D2-40 immunohistochemical analysis of pediatric vascular tumors reveals positivity in kaposiform hemangioendothelioma. Mod Pathol (2005) 1.09
CLOVE(S) syndrome: expanding the acronym. Am J Med Genet A (2009) 1.09
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformation. Hum Mutat (2013) 1.09
Complex pancreatic vascular anomalies in children. J Pediatr Surg (2006) 1.09
Mandibular deformity in hemifacial microsomia: a reassessment of the Pruzansky and Kaban classification. Plast Reconstr Surg (2014) 1.09
Primary lung tumors in children and adolescents: a 90-year experience. J Pediatr Surg (2010) 1.08
Imaging characteristics of blue rubber bleb nevus syndrome. AJR Am J Roentgenol (2003) 1.08
Comparison of pediatric emergency physicians' and surgeons' evaluation and diagnosis of appendicitis. Acad Emerg Med (2008) 1.08
Incidence of cranial asymmetry in healthy newborns. Pediatrics (2002) 1.07
Vascular anomalies. Surg Clin North Am (2006) 1.07
Swine-origin influenza a (H1N1) viral infection in children: initial chest radiographic findings. Radiology (2009) 1.07
Misdiagnosis of Klippel-Trenaunay syndrome. Intern Med (2014) 1.07