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Journal Abstract Search

197 related items for PubMed ID: 9056553

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  • 3. Application of DNA-based tests for diagnosis of spinal muscular atrophy in Saudi Arabia.
    al-Rajeh S, Majumdar R, Awada A, al-Jumah M.
    East Mediterr Health J; 1999 Nov; 5(6):1225-9. PubMed ID: 11924116
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  • 4. [Detection of SMN gene deletions in spinal muscular atrophy].
    Yang T, Yuan L, Liu T, Zhou W, Wu H, Zhao S, Shun L, Huo L, Ma S, Lin Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr 10; 15(2):95-7. PubMed ID: 9531649
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  • 5. Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene.
    Gambardella A, Mazzei R, Toscano A, Annesi G, Pasqua A, Annesi F, Quattrone F, Oliveri RL, Valentino P, Bono F, Aguglia U, Zappia M, Vita G, Quattrone A.
    Ann Neurol; 1998 Nov 10; 44(5):836-9. PubMed ID: 9818944
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  • 7. Deletions in the SMN and NAIP genes in patients with spinal muscular atrophy in Croatia.
    Sertić J, Barisić N, Sostarko M, Bosnjak N, Culić V, Cvitanović L, Ferencak G, Brzović Z, Stavljenić-Rukavina A.
    Coll Antropol; 1997 Dec 10; 21(2):487-92. PubMed ID: 9439064
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  • 9. Prenatal diagnosis of spinal muscular atrophy in Turkish families.
    Erdem H, Dayangaç D, Pehlivan S, Topaloglu H.
    Cent Eur J Public Health; 2001 Feb 10; 9(1):35-7. PubMed ID: 11243588
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  • 10. Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients.
    Mrad R, Dorboz I, Ben Jemaa L, Maazoul F, Trabelsi M, Chaabouni M, Mlaiki B, Miladi N, Hentati F, Chaabouni H.
    Tunis Med; 2006 Aug 10; 84(8):465-9. PubMed ID: 17175684
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  • 11. Deletion analysis of Bulgarian SMA families.
    Jordanova A, Stoyanova V, Uzunova M, Litvinenko I, Kremensky I.
    Hum Mutat; 1998 Aug 10; 12(1):33-8. PubMed ID: 9633817
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  • 12. SMA carrier testing--validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion.
    Scheffer H, Cobben JM, Mensink RG, Stulp RP, van der Steege G, Buys CH.
    Eur J Hum Genet; 2000 Feb 10; 8(2):79-86. PubMed ID: 10757638
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  • 14. High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients.
    Bouhouche A, Benomar A, Birouk N, Bouslam N, Ouazzani R, Yahyaoui M, Chkili T.
    J Neurol; 2003 Oct 10; 250(10):1209-13. PubMed ID: 14586604
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  • 15. [Survival motor neuron gene and neuronal apoptosis inhibitory protein gene deletion in patients with spinal muscular atrophy].
    Ma S, Yuan L, Liu T, Yang T, Zhou W, Wu H.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2000 Dec 10; 22(6):551-4. PubMed ID: 12903402
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  • 19. NAIP-deletion analysis in Malaysian patients with spinal muscular atrophy.
    Watihayati MS, Zabidi AM, Tang TH, Nishio H, Zilfalil BA.
    Kobe J Med Sci; 2007 Dec 10; 53(4):171-5. PubMed ID: 17932457
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  • 20. Correlation between severity and SMN protein level in spinal muscular atrophy.
    Lefebvre S, Burlet P, Liu Q, Bertrandy S, Clermont O, Munnich A, Dreyfuss G, Melki J.
    Nat Genet; 1997 Jul 10; 16(3):265-9. PubMed ID: 9207792
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