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440 related items for PubMed ID: 18533950

  • 1. SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy.
    Tran VK, Sasongko TH, Hong DD, Hoan NT, Dung VC, Lee MJ, Gunadi, Takeshima Y, Matsuo M, Nishio H.
    Pediatr Int; 2008 Jun; 50(3):346-51. PubMed ID: 18533950
    [Abstract] [Full Text] [Related]

  • 2. Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.
    Watihayati MS, Fatemeh H, Marini M, Atif AB, Zahiruddin WM, Sasongko TH, Tang TH, Zabidi-Hussin ZA, Nishio H, Zilfalil BA.
    Brain Dev; 2009 Jan; 31(1):42-5. PubMed ID: 18842367
    [Abstract] [Full Text] [Related]

  • 3. 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 Jan; 53(4):171-5. PubMed ID: 17932457
    [Abstract] [Full Text] [Related]

  • 4. The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study.
    Zhang Y, He J, Zhang Y, Li L, Tang X, Wang L, Guo J, Jin C, Tighe S, Zhang Y, Zhu Y, Zhu B.
    Medicine (Baltimore); 2020 Jan; 99(3):e18809. PubMed ID: 32011487
    [Abstract] [Full Text] [Related]

  • 5. Genotype-phenotype correlation of SMN locus genes in spinal muscular atrophy patients from India.
    Kesari A, Idris MM, Chandak GR, Mittal B.
    Exp Mol Med; 2005 Jun 30; 37(3):147-54. PubMed ID: 16000867
    [Abstract] [Full Text] [Related]

  • 6. Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.
    He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N, Chen WJ.
    Gene; 2013 Apr 15; 518(2):325-9. PubMed ID: 23352792
    [Abstract] [Full Text] [Related]

  • 7. Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Indian patients.
    Dastur RS, Gaitonde PS, Khadilkar SV, Udani VP, Nadkarni JJ.
    Neurol India; 2006 Sep 15; 54(3):255-9. PubMed ID: 16936383
    [Abstract] [Full Text] [Related]

  • 8. [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 15; 40(6):401-4. PubMed ID: 11798607
    [Abstract] [Full Text] [Related]

  • 9. Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy.
    Feldkötter M, Schwarzer V, Wirth R, Wienker TF, Wirth B.
    Am J Hum Genet; 2002 Feb 15; 70(2):358-68. PubMed ID: 11791208
    [Abstract] [Full Text] [Related]

  • 10. Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy.
    Zapletalová E, Hedvicáková P, Kozák L, Vondrácek P, Gaillyová R, Maríková T, Kalina Z, Jüttnerová V, Fajkus J, Fajkusová L.
    Neuromuscul Disord; 2007 Jun 15; 17(6):476-81. PubMed ID: 17475491
    [Abstract] [Full Text] [Related]

  • 11. Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy.
    Al-Jumah M, Majumdar R, Al-Rajeh S, Awada A, Chaves-Carbello E, Salih M, Al-Shahwan S, Al-Subiey K, Al-Uthaim S.
    Saudi Med J; 2003 Oct 15; 24(10):1052-4. PubMed ID: 14578966
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 84(8):465-9. PubMed ID: 17175684
    [Abstract] [Full Text] [Related]

  • 13. Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy.
    Taylor JE, Thomas NH, Lewis CM, Abbs SJ, Rodrigues NR, Davies KE, Mathew CG.
    Eur J Hum Genet; 1998 Aug 15; 6(5):467-74. PubMed ID: 9801871
    [Abstract] [Full Text] [Related]

  • 14. Molecular analysis of the SMN1 and NAIP genes in Iranian patients with spinal muscular atrophy.
    Derakhshandeh-Peykar P, Esmaili M, Ousati-Ashtiani Z, Rahmani M, Babrzadeh F, Farshidi S, Attaran E, Sajedifar MM, Farhud DD.
    Ann Acad Med Singap; 2007 Nov 15; 36(11):937-41. PubMed ID: 18071605
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  • 16. Hydroxyurea enhances SMN2 gene expression in spinal muscular atrophy cells.
    Grzeschik SM, Ganta M, Prior TW, Heavlin WD, Wang CH.
    Ann Neurol; 2005 Aug 15; 58(2):194-202. PubMed ID: 16049920
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  • 20. Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity.
    Harada Y, Sutomo R, Sadewa AH, Akutsu T, Takeshima Y, Wada H, Matsuo M, Nishio H.
    J Neurol; 2002 Sep 15; 249(9):1211-9. PubMed ID: 12242541
    [Abstract] [Full Text] [Related]

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