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Journal Abstract Search

153 related items for PubMed ID: 9391899

  • 1. Limb-girdle muscular dystrophy or spinal muscular atrophy: a source of diagnostic confusion?
    Pogue R, Jackson T, Sayli B, Curtis A, Bushby KM.
    J Med Genet; 1997 Nov; 34(11):958-9. PubMed ID: 9391899
    [No Abstract] [Full Text] [Related]

  • 2. [Diagnostic image (29). Adult form of proximal spinal muscular atrophy].
    Bronner IM, Linssen WH, de Visser M.
    Ned Tijdschr Geneeskd; 2001 Mar 17; 145(11):530. PubMed ID: 11284287
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  • 7. Reply to Burghes.
    MacKenzie AE.
    Am J Hum Genet; 1998 Feb 17; 62(2):485-8. PubMed ID: 9463330
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  • 8. Molecular genetics of autosomal recessive spinal muscular atrophy.
    Rodrigues NR, Talbot K, Davies KE.
    Mol Med; 1996 Jul 17; 2(4):400-4. PubMed ID: 8827710
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  • 11. Rapid SMN1 deletion test using DHPLC to screen patients with spinal muscular atrophy.
    Sutomo R, Akutsu T, Takeshima Y, Nishio H, Sadewa AH, Harada Y, Matsuo M.
    Am J Med Genet; 2002 Nov 22; 113(2):225-6. PubMed ID: 12407717
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  • 12. Screening of deletions in SMN, NAIP and BTF2p44 genes in Turkish spinal muscular atrophy patients.
    Savas S, Gokgoz N, Kayserili H, Ozkinay F, Yuksel-Apak M, Kirdar B.
    Hum Hered; 2000 Nov 22; 50(3):162-5. PubMed ID: 10686493
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  • 13. [A study of survival motor neuron and neuronal apoptosis inhibitory protein gene in spinal muscular atrophy].
    Zhang L, Yang X, Xiao B.
    Zhonghua Nei Ke Za Zhi; 2001 Jun 22; 40(6):401-4. PubMed ID: 11798607
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  • 18. Deletion analysis in Turkish patients with spinal muscular atrophy.
    Erdem H, Pehlivan S, Topaloglu H, Ozgüç M.
    Brain Dev; 1999 Mar 22; 21(2):86-9. PubMed ID: 10206524
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  • 20. Comment on SMN2 deletion in childhood-onset spinal muscular atrophy.
    Ogino S, Van Deerlin VM, Wilson RB.
    Am J Med Genet; 2002 May 01; 109(3):243-4; author reply 245. PubMed ID: 11977189
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