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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

138 related items for PubMed ID: 9044574

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  • 5. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
    Boylan KB, Cornblath DR.
    Ann Neurol; 1992 Sep; 32(3):404-7. PubMed ID: 1416812
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  • 10. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.
    Wang CH, Carter TA, Das K, Xu J, Ross BM, Penchaszadeh GK, Gilliam TC.
    Ann Neurol; 1997 Jul; 42(1):41-9. PubMed ID: 9225684
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  • 11. [Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study].
    Ben Hamida M, Hentati F, Chebbi N, Mhiri C, Ayed K, Hamzaoui K.
    Rev Neurol (Paris); 1988 Jul; 144(11):737-47. PubMed ID: 3231963
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  • 15. [Chronic spinal amyotrophy with paralysis of the vocal cords: Young-Harper syndrome].
    Serratrice G, Pellissier JF, Gastaut JL, Desnuelle C.
    Rev Neurol (Paris); 1984 Jul; 140(11):657-8. PubMed ID: 6505493
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  • 19. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
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  • 20. Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy.
    Ben Hamida C, Soussi-Yanicostas N, Butler-Browne GS, Bejaoui K, Hentati F, Ben Hamida M.
    Muscle Nerve; 1994 Apr; 17(4):400-10. PubMed ID: 8170486
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