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2. 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]
3. Dominant olivopontocerebellar atrophy with dementia and extrapyramidal signs: report of a family through three generations. Konigsmark BW, Lipton HL. Birth Defects Orig Artic Ser; 1971 Feb; 7(1):178-91. PubMed ID: 5173358 [Abstract] [Full Text] [Related]
7. Autonomic nerve calcification and peripheral neuropathy in olivopontocerebellar atrophy. Staal A, Stefanko SZ, Busch HF, Jennekens FG, De Bruinj WC. J Neurol Sci; 1981 Sep; 51(3):383-94. PubMed ID: 7276985 [Abstract] [Full Text] [Related]
8. Olivopontocerebellar atrophy in children: a report of seven cases in two families. Colan RV, Snead OC, Ceballos R. Ann Neurol; 1981 Oct; 10(4):355-63. PubMed ID: 7316488 [Abstract] [Full Text] [Related]
15. Disorders of ocular motility in the olivopontocerebellar atrophies. Lepore FE. Adv Neurol; 1984 Oct; 41():97-103. PubMed ID: 6388272 [No Abstract] [Full Text] [Related]
16. Histochemical mapping on the distribution of simple esterase and acetylcholinesterase in the medulla oblongata, cerebellum and spinal cord of mouse. Sood PP, Bohra MH. J Hirnforsch; 1977 Oct; 18(1):75-87. PubMed ID: 894017 [No Abstract] [Full Text] [Related]
17. [Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case]. Brion S, De Recondo J. Rev Neurol (Paris); 1967 May; 116(5):383-400. PubMed ID: 6052813 [No Abstract] [Full Text] [Related]
18. Glutamate and pyruvate dehydrogenase deficiency in spinocerebellar degeneration. Maruyama S, Yamaguchi T. Adv Neurol; 1984 May; 41():255-65. PubMed ID: 6437168 [No Abstract] [Full Text] [Related]
19. The hereditary ataxias. Skre H, Haugstad TS, Berg K. Prog Med Genet; 1985 May; 6():123-240. PubMed ID: 2425393 [No Abstract] [Full Text] [Related]