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.
87 related articles for article (PubMed ID: 5931801)
21. [A clinical study of spinocerebellar degeneration and its genetic background on Guam (author's transl)]. Murakami N; Chen KM; Gajdusek DC; Sobue I Rinsho Shinkeigaku; 1980 Apr; 20(4):271-9. PubMed ID: 7408331 [No Abstract] [Full Text] [Related]
22. [Heredo-degenerative disease with predominant extra-pyramidal symptoms]. Pépin B; Haguenau M; Job C Rev Neurol (Paris); 1975 Apr; 131(4):294-7. PubMed ID: 1224113 [No Abstract] [Full Text] [Related]
23. Spinocerebellar ataxia genes--expansion of the phenotype. Morrison PJ Ir Med J; 1998 Dec; 91(6):194, 196. PubMed ID: 10069123 [No Abstract] [Full Text] [Related]
24. [Roussy-Levy hereditary areflexic dysstasia. Its historical relation to Friedreich's disease, Charcot-Marie-Tooth atrophy and Dejerine-Sottas hypertrophic neuritis; the present status of the original family; the nosologic role of this entity]. Lapresle J Rev Neurol (Paris); 1982; 138(12):967-78. PubMed ID: 6763298 [TBL] [Abstract][Full Text] [Related]
26. A case of familial spinocerebellar degeneration with hypobetalipoproteinemia. Korula J; Namasivayam RK; Shadangi TN; Reddy PK; Raman PT Neurol India; 1976 Mar; 24(1):41-5. PubMed ID: 179026 [No Abstract] [Full Text] [Related]
27. [Transmission of a neurologic degeneration in a family for 4 generations manifested under variable semiologic aspects (pure pyramidal, pure cerebello-pyramidal involvement or involvement with abolition of reflexes and severe sensory disorders]. Mettey R; Hoppeler A; Gil R J Genet Hum; 1981 Sep; 29(3):227-34. PubMed ID: 7334346 [No Abstract] [Full Text] [Related]
28. [Effect of consanguinity on certain hereditary-degenerative spinocerebellar diseases in Tunisia]. el Gazzah L; Chalbi N; Ben Hamida M Tunis Med; 1985 Jan; 63():71-7. PubMed ID: 3992686 [No Abstract] [Full Text] [Related]
29. [Bilateral Ota's nevus with exclusively ocular localization and associated with spino-cerebellar degeneration syndrome]. Privat Y; Rousselot M; Faye I; Bellossi A; Ancelle G Bull Soc Fr Dermatol Syphiligr; 1968; 75(2):213-5. PubMed ID: 5677904 [No Abstract] [Full Text] [Related]
30. [Biochemical research in spino-cerebellar degeneration]. Badiu G Stud Cercet Neurol; 1968; 13(3):183-91. PubMed ID: 5670229 [No Abstract] [Full Text] [Related]
31. [Peculiar slowness of coordinated movements of the eyes frequently seen in cerebellar & spino-cerebellar degeneration; so-called viscosity of voluntary movements]. GARCIN R; MAN HX Rev Neurol (Paris); 1958 Jun; 98(6):672-3. PubMed ID: 13615078 [No Abstract] [Full Text] [Related]
32. [A case of spino-cerebellar degeneration]. RAYNAUD R; ESHOUGUES JR; JORDA M Alger Medicale; 1949 Feb; 53(2):68-70. PubMed ID: 18117880 [No Abstract] [Full Text] [Related]
33. Spinocerebellar degeneration with divergence paralysis as the earliest sign. Itoga E Hiroshima J Med Sci; 1980 Dec; 29(4):155-61. PubMed ID: 7204104 [No Abstract] [Full Text] [Related]
34. Specific messenger RNA changes in Joseph disease cerebella. Morrison MR; Rosenberg RN Ann Neurol; 1983 Jul; 14(1):73-9. PubMed ID: 6614873 [TBL] [Abstract][Full Text] [Related]
35. A case of the Roussy-Levy syndrome family. Bartosik-Psujek H; Stelmasiak Z Ann Univ Mariae Curie Sklodowska Med; 2001; 56():393-5. PubMed ID: 11977346 [TBL] [Abstract][Full Text] [Related]
36. [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)]. Roger J; Pellissier JF; Dravet C; Bureau-Paillas M; Arnoux M; Larrieu JL Rev Neurol (Paris); 1982; 138(3):187-200. PubMed ID: 6810437 [TBL] [Abstract][Full Text] [Related]
37. [Anatomical & clinical data on epilepsy. III. Spino-cerebellar degeneration with involuntary unilateral movements of athetosic type in an epileptic mental defective]. COLLE G Acta Neurol Psychiatr Belg; 1958 Feb; 58(2):114-23. PubMed ID: 13532576 [No Abstract] [Full Text] [Related]
38. An interesting case of Roussy-Levy syndrome inherited as autosomal dominant with diabetes mellitus. Garg SC; Singh N; Singh H; Thapar A J Assoc Physicians India; 1983 Jul; 31(7):467-8. PubMed ID: 6654813 [No Abstract] [Full Text] [Related]