These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 10434676)

  • 1. [Wohlfart-Kugelberg-Welander disease (SMA type III)].
    Hirayama Y; Osawa M
    Ryoikibetsu Shokogun Shirizu; 1999; (27 Pt 2):371-4. PubMed ID: 10434676
    [No Abstract]   [Full Text] [Related]  

  • 2. SMA type 2 unrelated to chromosome 5q13.
    Nevo Y; Kramer U; Legum C; Shomrat R; Fatal A; Soffer D; Harel S; Shapira Y
    Am J Med Genet; 1998 Jan; 75(2):193-5. PubMed ID: 9450884
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular basis of spinal muscular atrophy: th SMN gene].
    Tizzano E; Baiget M
    Neurologia; 2000 Nov; 15(9):393-400. PubMed ID: 11195146
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests.
    Botta A; Tacconelli A; Bagni I; Giardina E; Bonifazi E; Pietropolli A; Clementi M; Novelli G
    Neurology; 2005 Nov; 65(10):1631-5. PubMed ID: 16301493
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deletion analysis of Bulgarian SMA families.
    Jordanova A; Stoyanova V; Uzunova M; Litvinenko I; Kremensky I
    Hum Mutat; 1998; 12(1):33-8. PubMed ID: 9633817
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 24(10):1052-4. PubMed ID: 14578966
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 250(10):1209-13. PubMed ID: 14586604
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 53(4):171-5. PubMed ID: 17932457
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SMN2 deletion in childhood-onset spinal muscular atrophy.
    Cobben JM; de Visser M
    Am J Med Genet; 2002 May; 109(3):246; author reply 247. PubMed ID: 11977191
    [No Abstract]   [Full Text] [Related]  

  • 11. Comment on SMN2 deletion in childhood-onset spinal muscular atrophy.
    Ogino S; Van Deerlin VM; Wilson RB
    Am J Med Genet; 2002 May; 109(3):243-4; author reply 245. PubMed ID: 11977189
    [No Abstract]   [Full Text] [Related]  

  • 12. Spinal muscular atrophy: clinical classification and disease heterogeneity.
    Russman BS
    J Child Neurol; 2007 Aug; 22(8):946-51. PubMed ID: 17761648
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 84(8):465-9. PubMed ID: 17175684
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Quantitative analysis of SMN gene copies in spinal muscular atrophy].
    Ding HX; Yang XS; Xiao B; Wu ZG; Zhang LF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):153-5. PubMed ID: 15079799
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetically confirmed spinal muscular atrophy type III with epilepsy, cerebral hypoperfusion, and parahippocampal gyrus atrophy].
    Higashi K; Nakagawa M; Higuchi I; Saito K; Osame M
    Rinsho Shinkeigaku; 2000 Apr; 40(4):334-8. PubMed ID: 10967649
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spinal muscular atrophy: recent advances and future prospects.
    Nicole S; Diaz CC; Frugier T; Melki J
    Muscle Nerve; 2002 Jul; 26(1):4-13. PubMed ID: 12115944
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).
    Wirth B
    Hum Mutat; 2000; 15(3):228-37. PubMed ID: 10679938
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of the survival motor neuron and neuronal apoptosis inhibitory protein genes in Malay patients with Spinal Muscular Atrophy.
    Zilfalil BA; Zabidi-Hussin AM; Watihayati MS; Rozainah MY; Naing L; Sutomo R; Nishio H; Narazah MY; Matsuo M
    Med J Malaysia; 2004 Oct; 59(4):512-4. PubMed ID: 15779584
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 113(2):225-6. PubMed ID: 12407717
    [No Abstract]   [Full Text] [Related]  

  • 20. [Molecular biology of SMA (spinal muscular atrophy)].
    Kataoka N
    Tanpakushitsu Kakusan Koso; 2003 Mar; 48(4 Suppl):524-31. PubMed ID: 12696163
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.