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 *

378 related articles for article (PubMed ID: 17761648)

  • 1. 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]  

  • 2. 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]  

  • 3. Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy.
    Arkblad EL; Darin N; Berg K; Kimber E; Brandberg G; Lindberg C; Holmberg E; Tulinius M; Nordling M
    Neuromuscul Disord; 2006 Dec; 16(12):830-8. PubMed ID: 17049859
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy.
    Beattie CE; Carrel TL; McWhorter ML
    J Child Neurol; 2007 Aug; 22(8):995-1003. PubMed ID: 17761655
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients.
    Gamez J; Also E; Alias L; Corbera-Bellalta M; Barceló MJ; Centeno M; Raguer N; Gratacós M; Baiget M; Tizzano EF
    Clin Neurol Neurosurg; 2007 Dec; 109(10):844-8. PubMed ID: 17850955
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spinal muscular atrophy carrier screening by multiplex polymerase chain reaction using dried blood spot on filter paper.
    Majumdar R; Rehana Z; Al Jumah M; Fetaini N
    Ann Hum Genet; 2005 Mar; 69(Pt 2):216-21. PubMed ID: 15720302
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spinal muscular atrophy diagnostics.
    Prior TW
    J Child Neurol; 2007 Aug; 22(8):952-6. PubMed ID: 17761649
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease.
    Monani UR
    Neuron; 2005 Dec; 48(6):885-96. PubMed ID: 16364894
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.
    Chen WJ; Wu ZY; Lin MT; Su JF; Lin Y; Murong SX; Wang N
    Arch Neurol; 2007 Feb; 64(2):225-31. PubMed ID: 17296838
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severity.
    Akutsu T; Nishio H; Sumino K; Takeshima Y; Tsuneishi S; Wada H; Takada S; Matsuo M; Nakamura H
    Kobe J Med Sci; 2002 Apr; 48(1-2):25-31. PubMed ID: 11912351
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis and biological evaluation of novel 2,4-diaminoquinazoline derivatives as SMN2 promoter activators for the potential treatment of spinal muscular atrophy.
    Thurmond J; Butchbach ME; Palomo M; Pease B; Rao M; Bedell L; Keyvan M; Pai G; Mishra R; Haraldsson M; Andresson T; Bragason G; Thosteinsdottir M; Bjornsson JM; Coovert DD; Burghes AH; Gurney ME; Singh J
    J Med Chem; 2008 Feb; 51(3):449-69. PubMed ID: 18205293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Animal models of spinal muscular atrophy.
    Schmid A; DiDonato CJ
    J Child Neurol; 2007 Aug; 22(8):1004-12. PubMed ID: 17761656
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and genetic study of spinal muscular atrophies in Oman.
    Koul R; Al Futaisi A; Chacko A; Rao V; Simsek M; Muralitharan S; Ganguly SS; Bayoumi R
    J Child Neurol; 2007 Oct; 22(10):1227-30. PubMed ID: 17940251
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular mechanisms of spinal muscular atrophy.
    Sumner CJ
    J Child Neurol; 2007 Aug; 22(8):979-89. PubMed ID: 17761653
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evidence of a segregation ratio distortion of SMN1 alleles in spinal muscular atrophy.
    Alias L; Barceló MJ; Gich I; Estapé M; Parra J; Amenedo M; Baiget M; Tizzano EF
    Eur J Hum Genet; 2007 Oct; 15(10):1090-3. PubMed ID: 17625510
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Nucleotide differences in SMN1 and SMN2 gene.
    Kesari A; Mittal B
    Prenat Diagn; 2004 May; 24(5):398. PubMed ID: 15164419
    [No Abstract]   [Full Text] [Related]  

  • 20. A new splice site mutation in the SMN1 gene causes discrepant results in SMN1 deletion screening approaches.
    Eggermann T; Eggermann K; Elbracht M; Zerres K; Rudnik-Schöneborn S
    Neuromuscul Disord; 2008 Feb; 18(2):146-9. PubMed ID: 18155522
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.