BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

333 related articles for article (PubMed ID: 12654964)

  • 21. 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]  

  • 22. Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.
    Burlet P; Bürglen L; Clermont O; Lefebvre S; Viollet L; Munnich A; Melki J
    J Med Genet; 1996 Apr; 33(4):281-3. PubMed ID: 8730281
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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; 40(6):401-4. PubMed ID: 11798607
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene.
    Parsons DW; McAndrew PE; Monani UR; Mendell JR; Burghes AH; Prior TW
    Hum Mol Genet; 1996 Nov; 5(11):1727-32. PubMed ID: 8922999
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 27(1):8-15. PubMed ID: 8677029
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.
    Sun Y; Grimmler M; Schwarzer V; Schoenen F; Fischer U; Wirth B
    Hum Mutat; 2005 Jan; 25(1):64-71. PubMed ID: 15580564
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Correlation between genotype and phenotype in Korean patients with spinal muscular atrophy.
    Cho K; Ryu K; Lee E; Won S; Kim J; Yoo OJ; Hahn S
    Mol Cells; 2001 Feb; 11(1):21-7. PubMed ID: 11266116
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular analysis of SMN1 and NAIP genes in Egyptian patients with spinal muscular atrophy.
    Essawi ML; Effat LK; Shanab GM; Al-Ettribi GM; El-Haronui AA; Karim AM
    Bratisl Lek Listy; 2007; 108(3):133-7. PubMed ID: 17682539
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A clinical and genetic study of spinal muscular atrophy.
    Mishra VN; Kalita J; Kesari A; Mitta B; Shankar SK; Misra UK
    Electromyogr Clin Neurophysiol; 2004; 44(5):307-12. PubMed ID: 15378871
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Deletion of SMN and NAIP genes in Korean patients with spinal muscular atrophy.
    Shin S; Park SS; Hwang YS; Lee KW; Chung SG; Lee YJ; Park MH
    J Korean Med Sci; 2000 Feb; 15(1):93-8. PubMed ID: 10719817
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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; 37(3):147-54. PubMed ID: 16000867
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. [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; 22(6):551-4. PubMed ID: 12903402
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Identification of T274I mutation in the SMN1 gene in a patient with spinal muscular atrophy].
    Jedrzejowska M; Wiszniewski W; Ryniewicz B; Hausmanowa-Petrusewicz I
    Med Wieku Rozwoj; 2002; 6(4):319-27. PubMed ID: 12810984
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Deletion of the SMN1 and NAIP genes in Vietnamese patients with spinal muscular atrophy.
    Nguyen DB; Sadewa AH; Takeshima Y; Sutomo R; Tran VK; Nguyen TN; Nguyen TH; Vu CD; Dang DH; Harada Y; Nishio H; Matsuo M
    Kobe J Med Sci; 2003; 49(3-4):55-8. PubMed ID: 14676483
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Descriptive epidemiology of spinal muscular atrophy type I in Estonia.
    Vaidla E; Talvik I; Kulla A; Kahre T; Hamarik M; Napa A; Metsvaht T; Piirsoo A; Talvik T
    Neuroepidemiology; 2006; 27(3):164-8. PubMed ID: 17035693
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.