Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus [PDF]
Mei-Hong Wen +3 more
core +1 more source
FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse model. [PDF]
Cornille M +19 more
europepmc +1 more source
Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome: A case report. [PDF]
Shi H, Yang J, Guo Q, Zhang M.
europepmc +1 more source
Severe chemosis and treatment following fronto-orbital advancement surgery for Crouzon syndrome: A case report. [PDF]
Wu SH +5 more
europepmc +1 more source
Phenotypic heterogeneity in Crouzon syndrome: A case of severe intracranial hypertension from isolated temporal squamosal suture synostosis with a de novo FGFR2 p.Cys342Tyr mutation. [PDF]
Liu B, Gu W, Min L, Wei J, Wang X.
europepmc +1 more source
Characterization of dental pulp stem cells isolated from a patient diagnosed with Crouzon syndrome. [PDF]
Torii D +3 more
europepmc +1 more source
A Lifelong Battle With Crouzon Syndrome: A Detailed Case Report of Extensive Craniofacial Surgeries and Complex Psychiatric Care. [PDF]
Gillela ST +4 more
europepmc +1 more source
Airway management of a child of Crouzon syndrome with midface distractor in situ. [PDF]
Manoharan KS, Rajan S, Paul J, Kumar L.
europepmc +1 more source
Unlocking the potential of allele-specific siRNA therapy: A novel approach for Crouzon syndrome. [PDF]
Di Rocco F, de Laurentis C.
europepmc +1 more source

