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Journal Abstract Search

893 related items for PubMed ID: 8595417

  • 1. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.
    Hahnen E, Forkert R, Marke C, Rudnik-Schöneborn S, Schönling J, Zerres K, Wirth B.
    Hum Mol Genet; 1995 Oct; 4(10):1927-33. PubMed ID: 8595417
    [Abstract] [Full Text] [Related]

  • 2. 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; 54(3):255-9. PubMed ID: 16936383
    [Abstract] [Full Text] [Related]

  • 3. Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes.
    Haider MZ, Moosa A, Dalal H, Habib Y, Reynold L.
    J Biomed Sci; 2001 Sep; 8(2):191-6. PubMed ID: 11287750
    [Abstract] [Full Text] [Related]

  • 4. 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; 21(2):487-92. PubMed ID: 9439064
    [Abstract] [Full Text] [Related]

  • 5. Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype.
    Velasco E, Valero C, Valero A, Moreno F, Hernández-Chico C.
    Hum Mol Genet; 1996 Feb; 5(2):257-63. PubMed ID: 8824882
    [Abstract] [Full Text] [Related]

  • 6. 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; 36(11):937-41. PubMed ID: 18071605
    [Abstract] [Full Text] [Related]

  • 7. Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents.
    Chang JG, Jong YJ, Lin SP, Soong BW, Tsai CH, Yang TY, Chang CP, Wang WS.
    Hum Genet; 1997 Oct; 100(5-6):577-81. PubMed ID: 9341874
    [Abstract] [Full Text] [Related]

  • 8. Clinical and molecular genetic features of congenital spinal muscular atrophy.
    Devriendt K, Lammens M, Schollen E, Van Hole C, Dom R, Devlieger H, Cassiman JJ, Fryns JP, Matthijs G.
    Ann Neurol; 1996 Nov; 40(5):731-8. PubMed ID: 8957014
    [Abstract] [Full Text] [Related]

  • 9. Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.
    Wang CH, Xu J, Carter TA, Ross BM, Dominski MK, Bellcross CA, Penchaszadeh GK, Munsat TL, Gilliam TC.
    Hum Mol Genet; 1996 Mar; 5(3):359-65. PubMed ID: 8852661
    [Abstract] [Full Text] [Related]

  • 10. Different molecular basis for spinal muscular atrophy in South African black patients.
    Stevens G, Yawitch T, Rodda J, Verhaart S, Krause A.
    Am J Med Genet; 1999 Oct 29; 86(5):420-6. PubMed ID: 10508982
    [Abstract] [Full Text] [Related]

  • 11. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy].
    Spiegel R, Hagmann A, Boltshauser E, Moser H.
    Schweiz Med Wochenschr; 1996 May 25; 126(21):907-14. PubMed ID: 8693311
    [Abstract] [Full Text] [Related]

  • 12. 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 25; 24(10):1052-4. PubMed ID: 14578966
    [Abstract] [Full Text] [Related]

  • 13. Deletion analysis of the SMN and NAIP genes in Kuwaiti patients with spinal muscular atrophy.
    Samilchuk E, D'Souza B, Bastaki L, al-Awadi S.
    Hum Genet; 1996 Nov 25; 98(5):524-7. PubMed ID: 8882869
    [Abstract] [Full Text] [Related]

  • 14. Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients.
    Omrani O, Bonyadi M, Barzgar M.
    Pediatr Int; 2009 Apr 25; 51(2):193-6. PubMed ID: 19405914
    [Abstract] [Full Text] [Related]

  • 15. SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severity.
    Simard LR, Rochette C, Semionov A, Morgan K, Vanasse M.
    Am J Med Genet; 1997 Oct 03; 72(1):51-8. PubMed ID: 9295075
    [Abstract] [Full Text] [Related]

  • 16. 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 03; 250(10):1209-13. PubMed ID: 14586604
    [Abstract] [Full Text] [Related]

  • 17. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings.
    Rudnik-Schöneborn S, Forkert R, Hahnen E, Wirth B, Zerres K.
    Neuropediatrics; 1996 Feb 03; 27(1):8-15. PubMed ID: 8677029
    [Abstract] [Full Text] [Related]

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  • 19. Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAs.
    Wirth B, Hahnen E, Morgan K, DiDonato CJ, Dadze A, Rudnik-Schöneborn S, Simard LR, Zerres K, Burghes AH.
    Hum Mol Genet; 1995 Aug 03; 4(8):1273-84. PubMed ID: 7581364
    [Abstract] [Full Text] [Related]

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