Below are the most recent publications written about "Craniosynostoses" by people in Profiles.
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Wu M, Massenburg BB, Villavisanis DF, Chang AE, Romeo DJ, Ng JJ, Napoli JA, Bartlett SP, Swanson JW, Taylor JA. The Evolution of Unicoronal Synostosis Correction: Long-Term Aesthetics of Fronto-Orbital Distraction versus Advancement. Plast Reconstr Surg. 2025 Jul 01; 156(1):105-116.
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Wu M, Vossough A, Massenburg BB, Romeo DJ, Ng JJ, Napoli JA, Swanson JW, Bartlett SP, Taylor JA. Mystery of the Muenke midface: spheno-occipital synchondrosis fusion and craniofacial skeletal patterns. Childs Nerv Syst. 2024 Nov; 40(11):3683-3691.
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Demczko MM, Liu TT, Napoli JA. Craniosynostosis in a patient with Fanconi-Bickel syndrome: a case report. J Pediatr Endocrinol Metab. 2022 Sep 27; 35(9):1201-1205.
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Cuddapah VA, Dubbs HA, Adang L, Kugler SL, McCormick EM, Zolkipli-Cunningham Z, Ortiz-Gonz?lez XR, McCormack S, Zackai E, Licht DJ, Falk MJ, Marsh ED. Understanding the phenotypic spectrum of ASXL-related disease: Ten cases and a review of the literature. Am J Med Genet A. 2021 06; 185(6):1700-1711.
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Legare JM, Pauli RM, Hecht JT, Bober MB, Smid CJ, Modaff P, Little ME, Rodriguez-Buritica DF, Serna ME, Alade AY, Liu C, Hoover-Fong JE, Hashmi SS. CLARITY: Co-occurrences in achondroplasia-craniosynostosis, seizures, and decreased risk of diabetes mellitus. Am J Med Genet A. 2021 04; 185(4):1168-1174.
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Vingan P, Halsey JN, Gagliardo C, Battiato JA, Fried A, Ciminello FS. Treatment of Osteomyelitic Bone Following Cranial Vault Reconstruction With Delayed Reimplantation of Sterilized Autologous Bone: A Novel Technique for Cranial Reconstruction in the Pediatric Patient. J Craniofac Surg. 2021 Jan-Feb 01; 32(1):338-340.
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Tolchin D, Yeager JP, Prasad P, Dorrani N, Russi AS, Martinez-Agosto JA, Haseeb A, Angelozzi M, Santen GWE, Ruivenkamp C, Mercimek-Andrews S, Depienne C, Kuechler A, Mikat B, Ludecke HJ, Bilan F, Le Guyader G, Gilbert-Dussardier B, Keren B, Heide S, Haye D, Van Esch H, Keldermans L, Ortiz D, Lancaster E, Krantz ID, Krock BL, Pechter KB, Arkader A, Medne L, DeChene ET, Calpena E, Melistaccio G, Wilkie AOM, Suri M, Foulds N, Begtrup A, Henderson LB, Forster C, Reed P, McDonald MT, McConkie-Rosell A, Thevenon J, Le Tanno P, Coutton C, Tsai ACH, Stewart S, Maver A, Gorazd R, Pichon O, Nizon M, Cogn? B, Isidor B, Martin-Coignard D, Stoeva R, Lefebvre V, Le Caignec C. De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas. Am J Hum Genet. 2020 06 04; 106(6):830-845.
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Pan H, Zhang H, Abraham P, Komatsu Y, Lyons K, Kaartinen V, Mishina Y. BmpR1A is a major type 1 BMP receptor for BMP-Smad signaling during skull development. Dev Biol. 2017 09 01; 429(1):260-270.
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Lu L, Harutyunyan K, Jin W, Wu J, Yang T, Chen Y, Joeng KS, Bae Y, Tao J, Dawson BC, Jiang MM, Lee B, Wang LL. RECQL4 Regulates p53 Function In Vivo During Skeletogenesis. J Bone Miner Res. 2015 Jun; 30(6):1077-89.
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Lin AE, Traum AZ, Sahai I, Keppler-Noreuil K, Kukolich MK, Adam MP, Westra SJ, Arts HH. Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patients. Am J Med Genet A. 2013 Nov; 161A(11):2762-76.