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6. Analysis of eye movements in members of a family with late-onset, dominantly inherited cerebellar ataxia. Zee DS; Cogan DG; Robinson DA; Engel WK Trans Am Neurol Assoc; 1975; 100():98-103. PubMed ID: 1084072 [No Abstract] [Full Text] [Related]
7. Nosology of congenital non-progressive cerebellar ataxia. Report on six cases in three families. Pfeiffer RA; Palm D; Jünemann G; Mandl-Kramer S; Heimann E Neuropadiatrie; 1974 Feb; 5(1):91-102. PubMed ID: 4406233 [No Abstract] [Full Text] [Related]
9. A family with autosomal dominant spinocerebellar ataxia, with electrophysiological findings. Frey HJ; Frey ML; Riekkinen PJ; Tuomola HO Ann Clin Res; 1973 Jun; 5(3):163-7. PubMed ID: 4127165 [No Abstract] [Full Text] [Related]
10. Periodic alternating nystagmus in a case of hereditary ataxia and its treatment with baclofen. Plant GT J Neurol Neurosurg Psychiatry; 1982 Oct; 45(10):937-8. PubMed ID: 7143015 [No Abstract] [Full Text] [Related]
11. Periodic alternating nystagmus in a case of hereditary ataxia and its treatment with baclofen. Plant GT J Neurol Neurosurg Psychiatry; 1982 Dec; 45(12):1170-1. PubMed ID: 7161616 [No Abstract] [Full Text] [Related]
12. A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy. Wadia NH Adv Neurol; 1984; 41():149-77. PubMed ID: 6093483 [No Abstract] [Full Text] [Related]
13. [Otoneurologic symptomatology in hereditary cerebellar ataxia (Pierre Marie disease)]. Kalinovskaia IIa; Gurskaia NZ Zh Nevropatol Psikhiatr Im S S Korsakova; 1980; 80(3):367-72. PubMed ID: 7395412 [TBL] [Abstract][Full Text] [Related]
14. Ectodermal dysplasia syndrome with eyebrow alopecia, ptosis, strabismus, nystagmus, joint laxity, cerebellar ataxia, and osteopenia. Zannolli R; Inchingolo G; Serracca L; Miracco C; De Santi MM; Malandrini A; Biagioli M; Perotti R; Baldi C; Nuti D; Polito E; Gonnelli S Am J Med Genet; 2002 Nov; 113(1):111-3. PubMed ID: 12400077 [No Abstract] [Full Text] [Related]
15. Familial periodic ataxia. Margolin DI; Nutt JG; Lovrien EW Trans Am Neurol Assoc; 1981; 106():53-7. PubMed ID: 7349006 [No Abstract] [Full Text] [Related]
16. Autosomal dominant spinocerebellar ataxia with slow eye movements-a common hereditary ataxia in Western India. Wadia RS; Amin RB; Divate UP; Divate PG; Sainani GS; Sardesai HV J Assoc Physicians India; 1976 Jun; 24(6):367-71. PubMed ID: 1022769 [No Abstract] [Full Text] [Related]