Results 141 to 150 of about 10,448 (224)

Proximal tibiofibular synostosis in HDP SPECT/CT bone scan: A case report. [PDF]

Radiol Case Rep
Teixeira EPA, Decorads CE, Castarède I, Boudabbous S, Garibotto V.   +4 more
europepmc   +1 more source

Operative and non-operative treatment of congenital radio-ulnar synostosis in children: Results from a multicenter study. [PDF]

J Child Orthop
Zarantonello P, Trisolino G, Senes FM, Di Gennaro GL, Antonioli D, Catena N, Culmone A, Stauffer A, Chiarella LS, Farr S.   +9 more
europepmc   +1 more source

A Novel Cut-out Syringe Scalp Retractor for Endoscopic Strip Craniectomy for Craniosynostosis-A Cost-Effective and Durable Alternative. [PDF]

Asian J Neurosurg
Mittal A, Mishra R, Chegondi R, Patel HJ, Shrivastava A.   +4 more
europepmc   +1 more source

Comparing effectiveness of conservative policy to craniofacial surgery in children with metopic synostosis: protocol for an observational cohort study on clinical outcomes, psychosocial well-being and costs in a Dutch academic hospital. [PDF]

BMJ Open
Tio P, van Staalduinen M, Okkerse J, Dulfer K, Erler N, Loudon S, Telleman M, Abdel-Alim T, Roshchupkin G, Heemskerk S, Polinder S, van Veelen ML, Bannink N, van Driel A, Faasse M, Ista E, Joosten K, Spoor J, Weissbach E, Kats J, Versnel SL, Pleumeekers M, Mathijssen I.   +22 more
europepmc   +1 more source

Tibiofibular Synostosis

ARC Journal of Orthopedics, 2018
openaire   +1 more source

Prevalence of Fusion Between Adjacent Thoracic Spinous Processes in Adult Cadavers. [PDF]

Cureus
Sharma PN, Jethva K, Vaishnani H, Joshi M, Gohil P, Kulkarni MM, Gandotra AR.   +6 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]

Radiol Case Rep
Liu B, Gu W, Min L, Wei J, Wang X.
europepmc   +1 more source

Editorial. "Horses for courses" Response [PDF]

, 2017
Borghi, A, Dunaway, D, Jeelani, NUO, Schievano, S   +3 more
core  

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

Dedicated sub 0.1 mSv 3DCT using MBIR in children with suspected craniosynostosis: quality assessment [PDF]

core   +1 more source