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4. 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 [TBL] [Abstract][Full Text] [Related]
5. [The clinical, neuropathological and nosological study on three generations of a family affected with olivopontocerebellar atrophy (author's transl)]. Moriuchi I; Kato H; Kaiya H; Yoshimura T; Iwato T Seishin Shinkeigaku Zasshi; 1975 May; 77(5):303-28. PubMed ID: 1236418 [No Abstract] [Full Text] [Related]
8. Dominant olivopontocerebellar degeneration and optic pathway atrophy: a family report. Triau E; Dom R; Ververken D; Carton H Clin Neuropathol; 1982; 1(2):67-72. PubMed ID: 7168919 [No Abstract] [Full Text] [Related]
9. Olivopontocerebellar atrophy with visual disturbances. An ophthalmologic investigation into four generations. de Jong PT; de Jong JG; de Jong-Ten Doeschate JM; Delleman JW Ophthalmology; 1980 Aug; 87(8):793-804. PubMed ID: 7443212 [TBL] [Abstract][Full Text] [Related]
10. [Striatonigral degeneration associated with olivopontocerebellar atrophy. Anatomo-clinical study of 3 cases. Nosologic discussion]. Gosset A; Pellissier JF; Delpuech F; Khalil R Rev Neurol (Paris); 1983; 139(2):125-39. PubMed ID: 6410487 [TBL] [Abstract][Full Text] [Related]
11. Lipoprotein disorder, cirrhosis, and olivopontocerebellar degeneration in two siblings. Agamanolis DP; Potter JL; Naito HK; Robinson HB; Kulasekaran T Neurology; 1986 May; 36(5):674-81. PubMed ID: 3703266 [TBL] [Abstract][Full Text] [Related]
12. Ataxia, chorea, seizures, and dementia. Pathologic features of a newly defined familial disorder. Farmer TW; Wingfield MS; Lynch SA; Vogel FS; Hulette C; Katchinoff B; Jacobson PL Arch Neurol; 1989 Jul; 46(7):774-9. PubMed ID: 2742549 [TBL] [Abstract][Full Text] [Related]
13. Anterior horn cell disease and olivopontocerebellar hypoplasia. Ryan MM; Cooke-Yarborough CM; Procopis PG; Ouvrier RA Pediatr Neurol; 2000 Aug; 23(2):180-4. PubMed ID: 11020648 [TBL] [Abstract][Full Text] [Related]
14. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 39-1980. N Engl J Med; 1980 Oct; 303(14):803-9. PubMed ID: 7412787 [No Abstract] [Full Text] [Related]
15. Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy. Duvoisin RC; Chokroverty S; Lepore F; Nicklas W Neurology; 1983 Oct; 33(10):1322-6. PubMed ID: 6684227 [TBL] [Abstract][Full Text] [Related]
16. [Glial changes in olivo-ponto-cerebellar atrophies and their significance for formal pathogenesis]. von Cramon D; Kelemen J Acta Neuropathol; 1973 Jun; 25(1):14-26. PubMed ID: 4727728 [No Abstract] [Full Text] [Related]
17. Reduction of noradrenaline in cerebellum of patients with olivopontocerebellar atrophy. Kish SJ; Shannak KS; Hornykiewicz O J Neurochem; 1984 May; 42(5):1476-8. PubMed ID: 6707646 [TBL] [Abstract][Full Text] [Related]
18. 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]