Results 131 to 140 of about 2,247 (229)

Virtual 3D planning of osteotomies for craniosynostoses and complex craniofacial malformations

, 2019
B. Laure, A. Louisy, Aline Joly, Nicolas Travers, Antoine Listrat, Arnaud Paré   +5 more
openalex   +2 more sources

SMAD6 variants in nonsyndromic craniosynostosis. [PDF]

Eur J Hum Genet, 2023
Timberlake AT.
europepmc   +1 more source

FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family. [PDF]

Genes (Basel), 2023
Schmetz A, Schaper J, Thelen S, Rana M, Klenzner T, Schaumann K, Beygo J, Surowy H, Lüdecke HJ, Wieczorek D.   +9 more
europepmc   +1 more source

FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset [PDF]

, 2016

core   +1 more source

Case Report: Three-dimensional characteristics of craniofacial morphology in facial asymmetry due to unilateral coronal synostosis. [PDF]

Front Dent Med
Fukunaga T, Shigemi S, Konno M, Uechi J, Yoshizawa M, Kishikawa A, Imai Y, Kitaura H, Mizoguchi I.   +8 more
europepmc   +1 more source

Early mandibular morphological differences in patients with FGFR2 and FGFR3-related syndromic craniosynostoses: A 3D comparative study

, 2020
Anne Morice, Raphaël Cornette, Amerigo Giudice, Corinne Collet, Giovanna Paternoster, Éric Arnaud, E. Galliani, Arnaud Picard, Laurence Legeai‐Mallet, Roman Hossein Khonsari   +9 more
openalex   +2 more sources

Hearing Loss in Syndromic Craniosynostoses: Introduction and Consideration of Mechanisms

, 2014
Nneamaka B. Agochukwu, Benjamin D. Solomon, Maximilian Muenke   +2 more
openalex   +1 more source

Sagittal craniosynostosis with Moebius syndrome; case illustration: first case in the literatüre. [PDF]

BMC Pediatr
Kuzucu P, Kale A, Asadov İ, Börcek AÖ.   +3 more
europepmc   +1 more source

S13-07 SESSION 13: HYPERTELORISM / CRANIOFACIAL CLEFTS FLOATING FRONTAL FLAP COMBINED WITH INVERTED U-SHAPED OSTEOTOMY PROCEDURE IN ORBITAL HYPERTELORISM SECONDARY TO CRANIOSYNOSTOSES

, 2019
B. Yang, Leah Chen
openalex   +1 more source

Unlocking the potential of allele-specific siRNA therapy: A novel approach for Crouzon syndrome. [PDF]

Mol Ther Nucleic Acids
Di Rocco F, de Laurentis C.
europepmc   +1 more source