Published in J Craniofac Surg on March 01, 2010
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An X chromosome gene, WTX, is commonly inactivated in Wilms tumor. Science (2007) 4.00
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Venous malformations of skeletal muscle. Plast Reconstr Surg (2002) 2.79
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Dexmedetomidine for pediatric sedation for computed tomography imaging studies. Anesth Analg (2006) 2.16
Corticosteroid suppression of VEGF-A in infantile hemangioma-derived stem cells. N Engl J Med (2010) 2.16
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Kaposiform hemangioendothelioma without Kasabach-Merritt phenomenon. J Am Acad Dermatol (2005) 1.77
Clinical effects and safety of rituximab for treatment of refractory pediatric autoimmune diseases. J Pediatr (2007) 1.75
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Cloning of an Alpha-TFEB fusion in renal tumors harboring the t(6;11)(p21;q13) chromosome translocation. Proc Natl Acad Sci U S A (2003) 1.73
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Increased expression of urinary matrix metalloproteinases parallels the extent and activity of vascular anomalies. Pediatrics (2005) 1.72
Targeting angiogenesis with a conjugate of HPMA copolymer and TNP-470. Nat Med (2004) 1.70
Fog2 is required for normal diaphragm and lung development in mice and humans. PLoS Genet (2005) 1.69
Mechanical ventilation guided by electrical impedance tomography in experimental acute lung injury. Crit Care Med (2013) 1.68
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Differentiation of NUT midline carcinoma by epigenomic reprogramming. Cancer Res (2011) 1.65
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
Fibroepithelial polyps causing ureteropelvic junction obstruction in children. J Urol (2003) 1.63
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
Hemoglobin Jamaica plain--a sickling hemoglobin with reduced oxygen affinity. N Engl J Med (2004) 1.59
Urinary hepcidin in congenital chronic anemias. Pediatr Blood Cancer (2007) 1.58
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MARCO is the major binding receptor for unopsonized particles and bacteria on human alveolar macrophages. J Immunol (2005) 1.53
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
Response to mercaptopurine for refractory autoimmune cytopenias in children. Pediatr Blood Cancer (2009) 1.49
Bleeding risks are higher in children versus adults given prophylactic platelet transfusions for treatment-induced hypoproliferative thrombocytopenia. Blood (2012) 1.48
Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease. Am J Med Genet A (2013) 1.46
Lower-extremity lymphedema and elevated body-mass index. N Engl J Med (2012) 1.45
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
Gorham-Stout disease and generalized lymphatic anomaly--clinical, radiologic, and histologic differentiation. Skeletal Radiol (2013) 1.44
Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations. Pediatr Blood Cancer (2010) 1.43
Transfusion complications in thalassemia patients: a report from the Centers for Disease Control and Prevention (CME). Transfusion (2013) 1.43
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
Hypersusceptibility of cystic fibrosis mice to chronic Pseudomonas aeruginosa oropharyngeal colonization and lung infection. Proc Natl Acad Sci U S A (2003) 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
Evaluation of the coagulation system in children with two-ventricle congenital heart disease. Ann Thorac Surg (2007) 1.39
Homocystinuria: an unrecognized cause of microvascular failure. Plast Reconstr Surg (2007) 1.39
Primary lymphedema: clinical features and management in 138 pediatric patients. Plast Reconstr Surg (2011) 1.38
X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation. Blood (2007) 1.38
Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura. Blood (2005) 1.37
Biodegradation of Inion fast-absorbing biodegradable plates and screws. J Craniofac Surg (2008) 1.35
Differential expression of CD146 in tissues and endothelial cells derived from infantile haemangioma and normal human skin. J Pathol (2003) 1.35
Wilms tumor chromatin profiles highlight stem cell properties and a renal developmental network. Cell Stem Cell (2010) 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
Genetic ablation of the CDP/Cux protein C terminus results in hair cycle defects and reduced male fertility. Mol Cell Biol (2002) 1.28
Safety and efficacy of pegylated interferon alpha-2a and ribavirin for the treatment of hepatitis C in patients with thalassemia. Haematologica (2008) 1.26
Defective RNA ribose synthesis in fibroblasts from patients with thiamine-responsive megaloblastic anemia (TRMA). Blood (2003) 1.26
Reversible severe combined immunodeficiency phenotype secondary to a mutation of the proton-coupled folate transporter. Clin Immunol (2009) 1.26
Systems-level regulation of microRNA networks by miR-130/301 promotes pulmonary hypertension. J Clin Invest (2014) 1.26
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
The frequency and management of asparaginase-related thrombosis in paediatric and adult patients with acute lymphoblastic leukaemia treated on Dana-Farber Cancer Institute consortium protocols. Br J Haematol (2011) 1.24
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
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
Primary synovial sarcoma of the chest: radiographic and clinicopathologic correlation. J Thorac Imaging (2003) 1.20
Diffuse capillary malformation with overgrowth: a clinical subtype of vascular anomalies with hypertrophy. J Am Acad Dermatol (2013) 1.19