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 *

292 related articles for article (PubMed ID: 18395445)

  • 1. Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders.
    Parkinson NJ; Baumer D; Rose-Morris A; Talbot K
    Neuromuscul Disord; 2008 May; 18(5):394-7. PubMed ID: 18395445
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Disorders of the motor neurone.
    Morrison KE; Harding AE
    Baillieres Clin Neurol; 1994 Aug; 3(2):431-45. PubMed ID: 7952856
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Motor neuron diseases. Present].
    Pou A
    Neurologia; 1996 Dec; 11 Suppl 5():1-6. PubMed ID: 9044569
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic disorders of motor neurons.
    Cole N; Siddique T
    Semin Neurol; 1999; 19(4):407-18. PubMed ID: 10716663
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lix1 knockout mouse does not exhibit spinal muscular atrophy phenotype.
    Wakeling EN; Fyfe JC
    J Hered; 2011; 102 Suppl 1():S32-9. PubMed ID: 21846745
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Identification of a battery of tests for drug candidate evaluation in the SMNDelta7 neonate model of spinal muscular atrophy.
    El-Khodor BF; Edgar N; Chen A; Winberg ML; Joyce C; Brunner D; Suárez-Fariñas M; Heyes MP
    Exp Neurol; 2008 Jul; 212(1):29-43. PubMed ID: 18455159
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The role of RNA processing in the pathogenesis of motor neuron degeneration.
    Bäumer D; Ansorge O; Almeida M; Talbot K
    Expert Rev Mol Med; 2010 Jul; 12():e21. PubMed ID: 20642879
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Role of electromyography in the diagnosis of motor neuron disorders.
    Hausmanowa-Petrusewicz I
    Neuropatol Pol; 1992; 30(3-4):187-97. PubMed ID: 1340912
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An approximately 140-kb deletion associated with feline spinal muscular atrophy implies an essential LIX1 function for motor neuron survival.
    Fyfe JC; Menotti-Raymond M; David VA; Brichta L; Schäffer AA; Agarwala R; Murphy WJ; Wedemeyer WJ; Gregory BL; Buzzell BG; Drummond MC; Wirth B; O'Brien SJ
    Genome Res; 2006 Sep; 16(9):1084-90. PubMed ID: 16899656
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the C9orf72 gene in spinal muscular atrophy patients.
    Alías L; Bernal S; Barceló MJ; Martínez-Hernández R; Martínez E; Baiget M; Tizzano EF
    Amyotroph Lateral Scler Frontotemporal Degener; 2014 Dec; 15(7-8):563-8. PubMed ID: 24998634
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Molecular genetics and clinical aspects of inherited disorders of nerve and muscle.
    Harding AE
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):600-4. PubMed ID: 1392132
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS.
    Meisler MH; Russ C; Montgomery KT; Greenway M; Ennis S; Hardiman O; Figlewicz DA; Quenneville NR; Conibear E; Brown RH
    Amyotroph Lateral Scler; 2008 Jun; 9(3):141-8. PubMed ID: 18574757
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder.
    Sasongko TH; Gunadi ; Yusoff S; Atif AB; Fatemeh H; Rani A; Marini M; Ab Aziz CB; Zabidi-Hussin ZA; Nishio H; Zilfalil BA
    Brain Dev; 2010 May; 32(5):385-9. PubMed ID: 19664890
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distal spinal muscular atrophy.
    Muthukrishnan J; Varadarajulu R; Mehta SR; Singh AP
    J Assoc Physicians India; 2003 Nov; 51():1113-5. PubMed ID: 15260402
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular diagnosis of spinal muscular atrophy in Egyptians.
    Shawky RM; Abd el-Aleem K; Rifaat MM; Moustafa A
    East Mediterr Health J; 2001; 7(1-2):229-37. PubMed ID: 12596974
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cellular and molecular approaches to motor neuron therapy in amyotrophic lateral sclerosis and spinal muscular atrophy.
    O'Connor DM; Boulis NM
    Neurosci Lett; 2012 Oct; 527(2):78-84. PubMed ID: 22579818
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.