Below are the most recent publications written about "Craniosynostoses" by people in Profiles.
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González-Del Angel A, Estandía-Ortega B, Alcántara-Ortigoza MA, Martínez-Cruz V, Gutiérrez-Tinajero DJ, Rasmussen A, Gómez-González CS. Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis. Am J Med Genet A. 2016 12; 170(12):3189-3196.
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Lam S, Fridley J, Desai VR, Srinivasan VM, Jea A, Luerssen TG, Pan IW. Pediatric National Surgical Quality Improvement Program: Useful for Quality Improvement in Craniosynostosis Surgery? J Craniofac Surg. 2016 May; 27(3):605-11.
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Ghali MG, Srinivasan VM, Jea A, Lam S. Craniosynostosis surgery: the legacy of Paul Tessier. Neurosurg Focus. 2014 Apr; 36(4):E17.
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Deschamps-Braly J, Hettinger P, el Amm C, Denny AD. Volumetric analysis of cranial vault distraction for cephalocranial disproportion. Pediatr Neurosurg. 2011; 47(6):396-405.
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Rangel-Castilla L, Hwang SW, Jea A, Whitehead WE, Curry DJ, Luerssen TG, Dauser RC. Development of secondary unilateral coronal suture synostosis with a sagittal suture synostosis in a nonsyndromic patient. J Neurosurg Pediatr. 2012 Feb; 9(2):116-8.
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Panchal J, Amirsheybani H, Gurwitch R, Cook V, Francel P, Neas B, Levine N. Neurodevelopment in children with single-suture craniosynostosis and plagiocephaly without synostosis. Plast Reconstr Surg. 2001 Nov; 108(6):1492-8; discussion 1499-500.
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Muenke M, Gripp KW, McDonald-McGinn DM, Gaudenz K, Whitaker LA, Bartlett SP, Markowitz RI, Robin NH, Nwokoro N, Mulvihill JJ, Losken HW, Mulliken JB, Guttmacher AE, Wilroy RS, Clarke LA, Hollway G, Adès LC, Haan EA, Mulley JC, Cohen MM, Bellus GA, Francomano CA, Moloney DM, Wall SA, Wilkie AO, et al. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Am J Hum Genet. 1997 Mar; 60(3):555-64.
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Mooney MP, Aston CE, Siegel MI, Losken HW, Smith TD, Burrows AM, Wenger SL, Caruso K, Siegel B, Ferrell RE. Craniosynostosis with autosomal dominant transmission in New Zealand white rabbits. J Craniofac Genet Dev Biol. 1996 Jan-Mar; 16(1):52-63.
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Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ. Further delineation of the Baller-Gerold syndrome. Am J Med Genet. 1993 Feb 15; 45(4):519-24.