Results 81 to 90 of about 809 (163)

Concurrent surgical management of pineoblastoma and Chiari type 1.5 malformation: a case report. [PDF]

BMC Surg
Yiğit H, Gökoğlu A.
europepmc   +1 more source

From FGFR2 mutations to precision management: a review of prenatal diagnosis and multidisciplinary interventions in apert syndrome. [PDF]

Front Pediatr
Li H, Shen J, Tang M, Wan S, Zhang S.
europepmc   +1 more source

Apert Syndrome: An Insight Into Dentofacial Features. [PDF]

Cureus, 2021
Jose B, Emmatty TB, Methippara JJ, Kumar K, Thampi NM.   +4 more
europepmc   +1 more source

Efficacy of 2 different fibroblast growth factor receptor-inhibitors in a patient with extrahepatic cholangiocarcinoma harboring an FGFR2 mutation: a case report. [PDF]

Oncologist
Galli-Vareia I, Szturz P, Voutsadakis IA, Villard N, Tsoumakidou G, Fleury M, Herrera G, Fasquelle F, Godat S, Digklia A.   +9 more
europepmc   +1 more source

Basilar Invagination With Chiari Type I Malformation and Atlanto-Axial Instability: A Rare Case Report. [PDF]

Cureus, 2023
Sanjay N, Y S C, Yadav K, Dudekula A.
europepmc   +1 more source

Type I Acrocephalosyndactyly [PDF]

, 2020
openaire   +1 more source

Coexistence of Two Rare Conditions Complicating the Other's Management: Propionic Acidemia and Apert Syndrome. [PDF]

Mol Syndromol
Ensert Cihan CK, Akar HT, Yıldız Y, Sogukpinar M, Utine GE, Çelik HT.   +5 more
europepmc   +1 more source

A unique presentation of Crouzon-like syndrome: Complex craniosynostosis in the absence of genetic mutations or familial predisposition - A case report. [PDF]

Surg Neurol Int, 2023
Vaja H, Patel SN, Vadher A, Patel M, Patel MB, Shah J.   +5 more
europepmc   +1 more source

A novel FGFR2 (S137W) mutation resulting in Apert syndrome: A case report. [PDF]

Medicine (Baltimore), 2020
Shi Q, Dai R, Wang R, Jing J, Yu X, Liu R, Liu Y.   +6 more
europepmc   +1 more source

Introductory Chapter: Acne and Acneiform Dermatoses [PDF]

, 2017
Gönül, Müzeyyen, Kartal, Selda Pelin
core   +1 more source