Results 151 to 160 of about 5,186 (188)

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

Delayed Postnatal Synostosis without Spheno-occipital Synchondrosis Fusion: A Curious Case of Apert Syndrome. [PDF]

Plast Reconstr Surg Glob Open
Ng JJ, Massenburg BB, Wu M, Romeo DJ, Swanson JW, Taylor JA, Bartlett SP.   +6 more
europepmc   +1 more source

Application of Tasman technique for congenital absence of nasal cartilage: A case report [PDF]

, 2019
Gadaleta, Dominick, Heffelfinger, Ryan N.   +1 more
core   +1 more source

A Procedure for Designing Custom-Made Implants for Forehead Augmentation in People Suffering from Apert Syndrome. [PDF]

J Med Syst, 2020
Mandolini M, Caragiuli M, Brunzini A, Mazzoli A, Pagnoni M.   +4 more
europepmc   +1 more source

Is the Apert foot an overlooked aspect of this rare genetic disease? Clinical findings and treatment options for foot deformities in Apert syndrome. [PDF]

BMC Musculoskelet Disord, 2020
Stauffer A, Farr S.
europepmc   +1 more source

[Apert syndrome].

Pediatria polska, 1989
A, Pyrkosz, W, Grzywna, A, Grzybowski
openaire   +1 more source

Apert syndrome: prenatal diagnosis challenge. [PDF]

BMJ Case Rep, 2019
Vieira C, Teixeira N, Cadilhe A, Reis I.
europepmc   +1 more source

Apert syndrome [PDF]

, 2020
openaire   +1 more source

Apert syndrome: Be aware of the 'dodgy' hip! [PDF]

BMJ Case Rep, 2018
Khan SA, Moores TS, Docker C.
europepmc   +1 more source