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Journal Abstract Search

162 related items for PubMed ID: 3760830

  • 1. [Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence].
    Ben Hamida M, Chaabouni H, Madani S, Boussen S, Samoud S, Letaief F, Mrabet A, Hentati F, Miladi N.
    J Genet Hum; 1986 Aug; 34(3-4):267-74. PubMed ID: 3760830
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  • 2. [Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].
    Ben Hamida M, Madani S, Zmerli S, Chami I, Annabi A, Jamoussi M, Marzouki M, Rachdi M, Samoud S, Talbi M.
    Rev Neurol (Paris); 1980 Aug; 136(8-9):495-508. PubMed ID: 7221327
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  • 3. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F.
    Rev Neurol (Paris); 1991 Aug; 147(12):798-808. PubMed ID: 1780608
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  • 4. [Degenerative changes in cerebrospinal fluid electrophoresis recordings during spinocerebellar hereditary degenerative disorders. A study of 111 cases (author's transl)].
    Ben Hamida M, El Younsi C, Isautier C.
    Rev Neurol (Paris); 1980 Aug; 136(1):25-32. PubMed ID: 6156484
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  • 6. [Clinical contribution to Raymond's familial cerebelloataxospasmodic disease; atypical cases of Marie's hereditary ataxia and of spastic spinal paraplegia of Strümpell-Lorrain type in 3 brothers].
    CHIARAMONTI E, NISTRI M.
    Riv Sper Freniatr Med Leg Alien Ment; 1950 Mar 31; 74(1):5-17. PubMed ID: 15424618
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  • 8. [Friedreich's disease in the department of neurology in Dakar].
    Ndiaye M, Ndao AK, Sene-Diouf F, Diop AG, Diagne M, Thiam A, Ndiaye MM, Ndiaye IP.
    Dakar Med; 2000 Mar 31; 45(2):151-3. PubMed ID: 15779173
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  • 9. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
    El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F.
    Arch Neurol; 2003 Jul 31; 60(7):982-8. PubMed ID: 12873855
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  • 11. [Clinical characteristics of hereditary ataxia].
    Sidorova OP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988 Jul 31; 88(3):13-8. PubMed ID: 3381607
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  • 12. Molecular genetics of hereditary ataxias.
    Banfi S, Zoghbi HY.
    Baillieres Clin Neurol; 1994 Aug 31; 3(2):281-95. PubMed ID: 7952848
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  • 18. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
    Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B.
    Brain; 2006 Sep 31; 129(Pt 9):2332-40. PubMed ID: 16672289
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  • 19. Pseudodominant Friedreich's ataxia with phenotypic heterogeneity.
    Panas M, Kalfakis N, Vassilopoulos D.
    Acta Neurol Scand; 2007 May 31; 115(5):364-6. PubMed ID: 17489949
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  • 20. [Effect of consanguinity on certain hereditary-degenerative spinocerebellar diseases in Tunisia].
    el Gazzah L, Chalbi N, Ben Hamida M.
    Tunis Med; 1985 Jan 31; 63():71-7. PubMed ID: 3992686
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