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Journal Abstract Search

107 related items for PubMed ID: 512678

  • 21. High incidence of spinal muscular atrophy type I (Werdnig - Hoffmann disease) in the Karaite community in Israel.
    Fried K, Mundel G.
    Clin Genet; 1977 Oct; 12(4):250-1. PubMed ID: 912942
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  • 22. Late-onset X-linked recessive spinal and bulbar muscular atrophy.
    Ringel SP, Lava NS, Treihaft MM, Lubs ML, Lubs HA.
    Muscle Nerve; 1978 Oct; 1(4):297-307. PubMed ID: 571530
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  • 23. Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature.
    Harding AE, Thomas PK.
    J Neurol Sci; 1980 Mar; 45(2-3):337-48. PubMed ID: 7365507
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  • 25. Autosomal recessive microcephaly with severe psychomotor retardation.
    Scheffer IE, Baraitser M, Wilson J, Godfrey C, Brett EM.
    Neuropediatrics; 1992 Feb; 23(1):53-6. PubMed ID: 1565220
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  • 27. [Clinical picture, pathogenesis and geneology of hereditary progressive spinal muscular atrophies].
    Nesterov LN, Sushcheva GP, Viatkina SIa, Novikova NP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Feb; 84(3):321-30. PubMed ID: 6326437
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  • 35. Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.
    Viollet L, Barois A, Rebeiz JG, Rifai Z, Burlet P, Zarhrate M, Vial E, Dessainte M, Estournet B, Kleinknecht B, Pearn J, Adams RD, Urtizberea JA, Cros DP, Bushby K, Munnich A, Lefebvre S.
    Ann Neurol; 2002 May; 51(5):585-92. PubMed ID: 12112104
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  • 36. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A, Yoshida K, Ikeda S.
    Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303
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  • 38. An unusual form of spinal muscular atrophy with mental retardation occurring in an inbred population.
    Staal A, Went LN, Busch HF.
    J Neurol Sci; 1975 May; 25(1):57-64. PubMed ID: 1141957
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  • 39. Spinal muscular atrophy: clinical spectrum and genetic mutations in Pakistani children.
    Ibrahim S, Moatter T, Saleem AF.
    Neurol India; 2012 May; 60(3):294-8. PubMed ID: 22824686
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  • 40. [X-chromosomal bulbospinal muscular atrophy (Kennedy syndrome)].
    Berkhoff M, Sturzenegger M, Spiegel R, Rösler KM, Hess CW.
    Schweiz Med Wochenschr; 1998 May 23; 128(21):817-23. PubMed ID: 9642748
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