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2. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'. Harding AE Brain; 1982 Mar; 105(Pt 1):1-28. PubMed ID: 7066668 [TBL] [Abstract][Full Text] [Related]
3. Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family. Harding AE; Diengdoh JV; Lees AJ J Neurol Neurosurg Psychiatry; 1984 Aug; 47(8):853-6. PubMed ID: 6470726 [TBL] [Abstract][Full Text] [Related]
4. [Progressive supranuclear palsy with familial occurrence of spinocerebellar degeneration]. Yamamura Y; Kito S; Itoga E; Kajiwara H Rinsho Shinkeigaku; 1982 Jul; 22(7):586-93. PubMed ID: 7172528 [No Abstract] [Full Text] [Related]
8. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea]. Iwabuchi K; Nakazawa Y; Akai J; Yagishita S; Amano N No To Shinkei; 1994 Jun; 46(6):563-71. PubMed ID: 8068439 [TBL] [Abstract][Full Text] [Related]
9. A spinocerebellar degeneration with X-linked inheritance. Spira PJ; McLeod JG; Evans WA Brain; 1979 Mar; 102(1):27-41. PubMed ID: 427531 [TBL] [Abstract][Full Text] [Related]
10. Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects. Seong E; Insolera R; Dulovic M; Kamsteeg EJ; Trinh J; Brüggemann N; Sandford E; Li S; Ozel AB; Li JZ; Jewett T; Kievit AJA; Münchau A; Shakkottai V; Klein C; Collins CA; Lohmann K; van de Warrenburg BP; Burmeister M Ann Neurol; 2018 Jun; 83(6):1075-1088. PubMed ID: 29604224 [TBL] [Abstract][Full Text] [Related]
11. A novel GBA2 gene missense mutation in spastic ataxia. Votsi C; Zamba-Papanicolaou E; Middleton LT; Pantzaris M; Christodoulou K Ann Hum Genet; 2014 Jan; 78(1):13-22. PubMed ID: 24252062 [TBL] [Abstract][Full Text] [Related]
13. [Genetic aspects of some spino-cerebellar degenerations]. Badiu G Stud Cercet Neurol; 1969; 14(5):311-24. PubMed ID: 4906012 [No Abstract] [Full Text] [Related]
14. Joseph disease: a multisystem degenerative disorder of the nervous system. Sachdev HS; Forno LS; Kane CA Neurology; 1982 Feb; 32(2):192-5. PubMed ID: 7198744 [TBL] [Abstract][Full Text] [Related]
16. Atypical hereditary spino-cerebellar degeneration. Description of a case with familial study. Pitrangeli A; Gessini L; Jandolo B; Occhipinti E Ital J Neurol Sci; 1981 Dec; 2(4):387-90. PubMed ID: 7333830 [No Abstract] [Full Text] [Related]
17. Neurological approaches to the inherited ataxias. Refsum S; Skre H Adv Neurol; 1978; 21():1-13. PubMed ID: 367114 [No Abstract] [Full Text] [Related]
18. The pathology of Machado-Joseph disease. Report of a possible homozygous case. Coutinho P; Guimarães A; Scaravilli F Acta Neuropathol; 1982; 58(1):48-54. PubMed ID: 7136516 [TBL] [Abstract][Full Text] [Related]