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PUBMED FOR HANDHELDS

Journal Abstract Search


120 related items for PubMed ID: 7483104

  • 21. [A familial case of Kennedy's X-linked bulbospinal amyotrophy].
    Muradian GT, Tunian IuS, Khachunts AS, Samvelian KG.
    Zh Nevrol Psikhiatr Im S S Korsakova; 1993; 93(2):84-6. PubMed ID: 8048316
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  • 25. Molecular genetics and clinical aspects of inherited disorders of nerve and muscle.
    Harding AE.
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):600-4. PubMed ID: 1392132
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  • 28. [X-linked recessive bulbospinal muscular atrophy (Kennedy's disease). A family study].
    Kaimen-Maciel DR, Medeiros M, Clímaco V, Kelian GR, da Silva LS, de Souza MM, Raskin S.
    Arq Neuropsiquiatr; 1998 Sep; 56(3B):639-45. PubMed ID: 9850762
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  • 29. [A weak man... X chromosome associated progressive bulbospinal neuropathy (or bulbospinal amyotrophy) or Kennedy syndrome].
    Ricard D, Sallansonnet-Froment M, De Greslan T.
    Rev Neurol (Paris); 2009 Feb; 165 Spec No 1():F29, F31. PubMed ID: 19623708
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  • 35. Kennedy disease: avoiding misdiagnosis.
    Paparounas K, Gotsi A, Syrrou M, Akritidis N.
    Arch Neurol; 2003 Jun; 60(6):893-4. PubMed ID: 12810497
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  • 36. [Tissue variability of androgen receptor gene in bulbospinal muscular atrophy--comparison of the number of CAG repeats between muscles and peripheral blood leukocytes].
    Nakajima H, Kimura F, Shinoda K, Ohsawa N, Nakagawa T, Shimizu A.
    Rinsho Shinkeigaku; 1993 Oct; 33(10):1103-5. PubMed ID: 8293617
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