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PUBMED FOR HANDHELDS

Journal Abstract Search


154 related items for PubMed ID: 712386

  • 1. Autosomal dominant spinal muscular atrophy: a clinical and genetic study.
    Pearn J.
    J Neurol Sci; 1978 Sep; 38(2):263-75. PubMed ID: 712386
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  • 2. A clinical and genetic study of spinal muscular atrophy of adult onset: the autosomal recessive form as a discrete disease entity.
    Pearn JH, Hudgson P, Walton JN.
    Brain; 1978 Dec; 101(4):591-606. PubMed ID: 737522
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  • 6. Distal spinal muscular atrophy. A clinical and genetic study of 8 kindreds.
    Pearn J, Hudgson P.
    J Neurol Sci; 1979 Oct; 43(2):183-91. PubMed ID: 512678
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  • 10. 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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  • 11. Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex.
    Yuill GM, Lynch PG.
    J Neurol Neurosurg Psychiatry; 1974 Mar; 37(3):316-23. PubMed ID: 4364274
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  • 12. Segregation analysis of chronic childhood spinal muscular atrophy.
    Pearn J.
    J Med Genet; 1978 Dec; 15(6):418-23. PubMed ID: 745213
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  • 14. The benign proximal spinal progressive muscular atrophies.
    Peters HA, Opitz JM, Goto I, Reese HH.
    Acta Neurol Scand; 1968 Dec; 44(5):542-60. PubMed ID: 5726730
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  • 16. Classification of spinal muscular atrophies.
    Pearn J.
    Lancet; 1980 Apr 26; 1(8174):919-22. PubMed ID: 6103267
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  • 18. Autosomal dominant familial spinal and bulbar muscular atrophy with gynecomastia.
    Ikezoe K, Yoshimura T, Taniwaki T, Matsuura E, Furuya H, Yamada T, Nagamatsu K, Kira J.
    Neurology; 1999 Dec 10; 53(9):2187-9. PubMed ID: 10599805
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