These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
147 related articles for article (PubMed ID: 513084)
1. Non-progressive cerebellar ataxia, aplasia of pupillary zone of iris, and mental subnormality (Gillespie's syndrome) affecting 3 members of a non-consanguineous family in 2 generations. Crawfurd MD; Harcourt RB; Shaw PA J Med Genet; 1979 Oct; 16(5):373-8. PubMed ID: 513084 [TBL] [Abstract][Full Text] [Related]
2. Gillespie's syndrome (incomplete aniridia, cerebellar ataxia and oligophrenia). François J; Lentini F; de Rouck F Ophthalmic Paediatr Genet; 1984 Apr; 4(1):29-32. PubMed ID: 6544390 [TBL] [Abstract][Full Text] [Related]
3. Gillespie's Syndrome with Minor Cerebellar Involvement and No Intellectual Disability Associated with a Novel ITPR1 Mutation: Report of a Case and Literature Review. Stendel C; Wagner M; Rudolph G; Klopstock T Neuropediatrics; 2019 Dec; 50(6):382-386. PubMed ID: 31340402 [TBL] [Abstract][Full Text] [Related]
4. Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites. Schurig V; Orman AV; Bowen P Am J Med Genet; 1981; 9(1):43-53. PubMed ID: 7246619 [TBL] [Abstract][Full Text] [Related]
5. The syndrome of congenital cerebellar ataxia, aniridia and mental retardation. Sarsfield JK Dev Med Child Neurol; 1971 Aug; 13(4):508-11. PubMed ID: 5558750 [No Abstract] [Full Text] [Related]
6. Hereditary ectodermal dysplasia, olivopontocerebellar degeneration, short stature, and hypogonadism. Rushton AR; Genel M J Med Genet; 1981 Oct; 18(5):335-9. PubMed ID: 7328612 [TBL] [Abstract][Full Text] [Related]
7. [Gillespie syndrome (incomplete aniridia, cerebellar ataxia and oligophrenia)]. François J; Lentini F Klin Monbl Augenheilkd; 1984 Apr; 184(4):313-5. PubMed ID: 6727263 [TBL] [Abstract][Full Text] [Related]
8. A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability. Kawarai T; Tajima A; Kuroda Y; Saji N; Orlacchio A; Terasawa H; Shimizu H; Kita Y; Izumi Y; Mitsui T; Imoto I; Kaji R J Neurol Neurosurg Psychiatry; 2016 Jun; 87(6):656-62. PubMed ID: 26157035 [TBL] [Abstract][Full Text] [Related]
9. Additional features of Gillespie syndrome in two Brazilian siblings with a novel ITPR1 homozygous pathogenic variant. Carvalho DR; Medeiros JEG; Ribeiro DSM; Martins BJAF; Sobreira NLM Eur J Med Genet; 2018 Mar; 61(3):134-138. PubMed ID: 29169895 [TBL] [Abstract][Full Text] [Related]
10. A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4. Mohamadian M; Ghandil P; Naseri M; Bahrami A; Momen AA J Clin Lab Anal; 2020 Nov; 34(11):e23484. PubMed ID: 33079427 [TBL] [Abstract][Full Text] [Related]
11. Autosomal recessive non-progressive ataxia with an early childhood debut. Kvistad PH; Dahl A; Skre H Acta Neurol Scand; 1985 Apr; 71(4):295-302. PubMed ID: 4003033 [TBL] [Abstract][Full Text] [Related]
12. A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze Family. Delague V; Bareil C; Bouvagnet P; Salem N; Chouery E; Loiselet J; Mégarbané A; Claustres M Neurogenetics; 2002 Mar; 4(1):23-7. PubMed ID: 12030328 [TBL] [Abstract][Full Text] [Related]
17. Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family. Bouhlal Y; Zouari M; Kefi M; Ben Hamida C; Hentati F; Amouri R J Neurogenet; 2008; 22(2):139-48. PubMed ID: 18569450 [TBL] [Abstract][Full Text] [Related]