Results 101 to 110 of about 5,083 (170)

Synchronous Cardiac Fibroma and Medulloblastoma in Gorlin Syndrome: A Paradigmatic Case and Narrative Review. [PDF]

Children (Basel)
Molteni M, Trocchio G, Verrico A, Derchi M, Stagnaro N, Di Giannatale A, Ghiorzo P, Montaguti A, Ramaglia A, Milanaccio C, Piccolo G, Garrè ML.   +11 more
europepmc   +1 more source

Prenatal diagnosis of Meier-Gorlin syndrome 7: a case presentation. [PDF]

BMC Pregnancy Childbirth, 2021
Li X, Zhang LZ, Yu L, Long ZL, Lin AY, Gou CY.   +5 more
europepmc   +1 more source

[Gorlin syndrome].

Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti, 2009
P, Plevová, V, Krutílková, A, Puchmajerová, L, Foretová   +3 more
openaire   +3 more sources

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome. [PDF]

Am J Med Genet A
Taliercio V, Zhao J, Boyden SE, Mao R, Bayrak-Toydemir P, Pflaum A, Palumbos J, Andrews A, Baldwin EE, Welt C, Fait M, Undiagnosed Diseases Network, Botto LD, Viskochil D.   +13 more
europepmc   +1 more source

Gorlin Syndrome: Sequential Digital Dermoscopy of Palpebral Basal Cell Carcinomas in a Patient Treated with Vismodegib. [PDF]

Dermatol Pract Concept, 2022
Mena-Vergara L, Silva-Astorga M, Carrasco-Cancino C, Muñoz-Uslar L.   +3 more
europepmc   +1 more source

A Case of Sustained Ventricular Tachycardia Secondary to a Cardiac Fibroma in a Patient With Gorlin Syndrome. [PDF]

Cureus
Moodie D, Paudel U, Fahed J, Zerihun W, Sigdel K.   +4 more
europepmc   +1 more source

Pediatric basal cell carcinoma burden and management preferences in Gorlin syndrome: A survey study. [PDF]

JAAD Int, 2021
Neale H, Breneiser JA, Hawryluk EB.
europepmc   +1 more source

Defining the Spectrum, Treatment and Outcome of Patients With Genetically Confirmed Gorlin Syndrome From the HIT-MED Cohort. [PDF]

Front Oncol, 2021
Kloth K, Obrecht D, Sturm D, Pietsch T, Warmuth-Metz M, Bison B, Mynarek M, Rutkowski S.   +7 more
europepmc   +1 more source

A Novel <i>PTCH1</i> Non-Canonical Splice Region Variant Associated with Gorlin Syndrome: A Case Report. [PDF]

Mol Syndromol
Smith MJ, Shell EJ, Burghel GJ, Carney M, Waller SJ, Hakim A, Evans DG.   +6 more
europepmc   +1 more source

Biallelic <i>GINS2</i> variant p.(Arg114Leu) causes Meier-Gorlin syndrome with craniosynostosis. [PDF]

J Med Genet, 2022
Nabais Sá MJ, Miller KA, McQuaid M, Koelling N, Wilkie AOM, Wurtele H, de Brouwer APM, Oliveira J.   +7 more
europepmc   +1 more source