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 *

104 related articles for article (PubMed ID: 20429685)

  • 1. Biomarkers of disease in a case of familial lower motor neuron ALS.
    Baumann F; Rose SE; Nicholson GA; Hutchinson N; Pannek K; Pettitt A; Mccombe PA; Henderson RD
    Amyotroph Lateral Scler; 2010 Oct; 11(5):486-9. PubMed ID: 20429685
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.
    Cudkowicz ME; McKenna-Yasek D; Chen C; Hedley-Whyte ET; Brown RH
    Ann Neurol; 1998 Jun; 43(6):703-10. PubMed ID: 9629839
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Objective markers for upper motor neuron involvement in amyotrophic lateral sclerosis].
    Iwata NK
    Brain Nerve; 2007 Oct; 59(10):1053-64. PubMed ID: 17969345
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Activation of microglial neuregulin1 signaling in the corticospinal tracts of ALS patients with upper motor neuron signs.
    Song F; Chiang P; Ravits J; Loeb JA
    Amyotroph Lateral Scler Frontotemporal Degener; 2014 Mar; 15(1-2):77-83. PubMed ID: 24229388
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluation of corticospinal tracts in ALS with diffusion tensor MRI and brainstem stimulation.
    Iwata NK; Aoki S; Okabe S; Arai N; Terao Y; Kwak S; Abe O; Kanazawa I; Tsuji S; Ugawa Y
    Neurology; 2008 Feb; 70(7):528-32. PubMed ID: 18268244
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diffusion tensor MRI of early upper motor neuron involvement in amyotrophic lateral sclerosis.
    Sach M; Winkler G; Glauche V; Liepert J; Heimbach B; Koch MA; Büchel C; Weiller C
    Brain; 2004 Feb; 127(Pt 2):340-50. PubMed ID: 14607785
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical electrophysiology of the upper and lower motor neuron in amyotrophic lateral sclerosis.
    Eisen A
    Semin Neurol; 2001 Jun; 21(2):141-54. PubMed ID: 11442323
    [TBL] [Abstract][Full Text] [Related]  

  • 8. SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis.
    Luigetti M; Madia F; Conte A; Marangi G; Zollino M; Del Grande A; Dileone M; Tonali PA; Sabatelli M
    Amyotroph Lateral Scler; 2009; 10(5-6):479-82. PubMed ID: 19922144
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diffusion tensor MRI as a diagnostic tool of upper motor neuron involvement in amyotrophic lateral sclerosis.
    Hong YH; Lee KW; Sung JJ; Chang KH; Song IC
    J Neurol Sci; 2004 Dec; 227(1):73-8. PubMed ID: 15546594
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Preserved slow conducting corticomotoneuronal projections in amyotrophic lateral sclerosis with autosomal recessive D90A CuZn-superoxide dismutase mutation.
    Weber M; Eisen A; Stewart HG; Andersen PM
    Brain; 2000 Jul; 123 ( Pt 7)():1505-15. PubMed ID: 10869061
    [TBL] [Abstract][Full Text] [Related]  

  • 11. F-Waves and the corticospinal lesion in amyotrophic lateral sclerosis.
    de Carvalho M; Scotto M; Lopes A; Swash M
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Sep; 3(3):131-6. PubMed ID: 12495574
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rapid disease progression correlates with instability of mutant SOD1 in familial ALS.
    Sato T; Nakanishi T; Yamamoto Y; Andersen PM; Ogawa Y; Fukada K; Zhou Z; Aoike F; Sugai F; Nagano S; Hirata S; Ogawa M; Nakano R; Ohi T; Kato T; Nakagawa M; Hamasaki T; Shimizu A; Sakoda S
    Neurology; 2005 Dec; 65(12):1954-7. PubMed ID: 16291929
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression.
    Keckarević D; Stević Z; Keckarević-Marković M; Kecmanović M; Romac S
    Amyotroph Lateral Scler; 2012 Feb; 13(2):237-40. PubMed ID: 22214314
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spreading in ALS: The relative impact of upper and lower motor neuron involvement.
    Gromicho M; Figueiral M; Uysal H; Grosskreutz J; Kuzma-Kozakiewicz M; Pinto S; Petri S; Madeira S; Swash M; de Carvalho M
    Ann Clin Transl Neurol; 2020 Jul; 7(7):1181-1192. PubMed ID: 32558369
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Quantitative objective markers for upper and lower motor neuron dysfunction in ALS.
    Mitsumoto H; Ulug AM; Pullman SL; Gooch CL; Chan S; Tang MX; Mao X; Hays AP; Floyd AG; Battista V; Montes J; Hayes S; Dashnaw S; Kaufmann P; Gordon PH; Hirsch J; Levin B; Rowland LP; Shungu DC
    Neurology; 2007 Apr; 68(17):1402-10. PubMed ID: 17452585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions.
    Ohi T; Nabeshima K; Kato S; Yazawa S; Takechi S
    J Neurol Sci; 2004 Oct; 225(1-2):19-25. PubMed ID: 15465081
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis.
    Luigetti M; Conte A; Madia F; Marangi G; Zollino M; Mancuso I; Dileone M; Del Grande A; Di Lazzaro V; Tonali PA; Sabatelli M
    Neurol Sci; 2009 Dec; 30(6):517-20. PubMed ID: 19685200
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Primary lateral sclerosis as a phenotypic manifestation of familial ALS.
    Brugman F; Wokke JH; Vianney de Jong JM; Franssen H; Faber CG; Van den Berg LH
    Neurology; 2005 May; 64(10):1778-9. PubMed ID: 15911810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel central motor conduction abnormality in D90A-homozygous patients with amyotrophic lateral sclerosis.
    Osei-Lah AD; Turner MR; Andersen PM; Leigh PN; Mills KR
    Muscle Nerve; 2004 Jun; 29(6):790-4. PubMed ID: 15170611
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS.
    Ricci C; Benigni M; Battistini S; Greco G; Torzini A; Giannini F
    Amyotroph Lateral Scler; 2010 Oct; 11(5):481-5. PubMed ID: 20331403
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.