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 *

351 related articles for article (PubMed ID: 15911810)

  • 1. 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]  

  • 2. 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]  

  • 3. Genetics of familial Amyotrophic lateral sclerosis.
    Ticozzi N; Tiloca C; Morelli C; Colombrita C; Poletti B; Doretti A; Maderna L; Messina S; Ratti A; Silani V
    Arch Ital Biol; 2011 Mar; 149(1):65-82. PubMed ID: 21412717
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS.
    Gordon PH; Cheng B; Katz IB; Mitsumoto H; Rowland LP
    Neurology; 2009 Jun; 72(22):1948-52. PubMed ID: 19487653
    [TBL] [Abstract][Full Text] [Related]  

  • 5. In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient.
    Niessen HG; Angenstein F; Sander K; Kunz WS; Teuchert M; Ludolph AC; Heinze HJ; Scheich H; Vielhaber S
    Exp Neurol; 2006 Oct; 201(2):293-300. PubMed ID: 16740261
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis.
    Dalla Bella E; Rigamonti A; Mantero V; Morbin M; Saccucci S; Gellera C; Mora G; Lauria G
    J Neurol Neurosurg Psychiatry; 2014 Sep; 85(9):1009-11. PubMed ID: 24591457
    [TBL] [Abstract][Full Text] [Related]  

  • 7. TDP-43 in differential diagnosis of motor neuron disorders.
    Dickson DW; Josephs KA; Amador-Ortiz C
    Acta Neuropathol; 2007 Jul; 114(1):71-9. PubMed ID: 17569066
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
    Watanabe M; Dykes-Hoberg M; Culotta VC; Price DL; Wong PC; Rothstein JD
    Neurobiol Dis; 2001 Dec; 8(6):933-41. PubMed ID: 11741389
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel SOD1 mutation in a young amyotrophic lateral sclerosis patient with a very slowly progressive clinical course.
    Georgoulopoulou E; Gellera C; Bragato C; Sola P; Chiari A; Bernabei C; Mandrioli J
    Muscle Nerve; 2010 Oct; 42(4):596-7. PubMed ID: 20740631
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Diffusion tensor imaging in sporadic and familial (D90A SOD1) forms of amyotrophic lateral sclerosis.
    Stanton BR; Shinhmar D; Turner MR; Williams VC; Williams SC; Blain CR; Giampietro VP; Catani M; Leigh PN; Andersen PM; Simmons A
    Arch Neurol; 2009 Jan; 66(1):109-15. PubMed ID: 19139308
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutational analysis of the Cu/Zn superoxide dismutase gene in a Catalan ALS population: should all sporadic ALS cases also be screened for SOD1?
    Gamez J; Corbera-Bellalta M; Nogales G; Raguer N; García-Arumí E; Badia-Canto M; Lladó-Carbó E; Alvarez-Sabín J
    J Neurol Sci; 2006 Aug; 247(1):21-8. PubMed ID: 16674979
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients.
    Alavi A; Nafissi S; Rohani M; Zamani B; Sedighi B; Shamshiri H; Fan JB; Ronaghi M; Elahi E
    Neurobiol Aging; 2013 May; 34(5):1516.e1-8. PubMed ID: 23062701
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
    Mackenzie IR; Bigio EH; Ince PG; Geser F; Neumann M; Cairns NJ; Kwong LK; Forman MS; Ravits J; Stewart H; Eisen A; McClusky L; Kretzschmar HA; Monoranu CM; Highley JR; Kirby J; Siddique T; Shaw PJ; Lee VM; Trojanowski JQ
    Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
    García-Redondo A; Bustos F; Juan Y Seva B; Del Hoyo P; Jiménez S; Campos Y; Martín MA; Rubio JC; Cañadillas F; Arenas J; Esteban J
    Muscle Nerve; 2002 Aug; 26(2):274-8. PubMed ID: 12210393
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees.
    Praline J; Guennoc AM; Vourc'h P; De Toffol B; Corcia P
    Amyotroph Lateral Scler; 2010; 11(1-2):154-6. PubMed ID: 20184517
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease.
    Takazawa T; Ikeda K; Hirayama T; Kawabe K; Nakamura Y; Ito H; Kano O; Yoshii Y; Tanaka F; Sobue G; Iwasaki Y
    Intern Med; 2010; 49(2):183-6. PubMed ID: 20075587
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS.
    Robertson J; Sanelli T; Xiao S; Yang W; Horne P; Hammond R; Pioro EP; Strong MJ
    Neurosci Lett; 2007 Jun; 420(2):128-32. PubMed ID: 17543992
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.
    Berdyński M; Kuźma-Kozakiewicz M; Ricci C; Kubiszewska J; Millecamps S; Salachas F; Łusakowska A; Carrera P; Meininger V; Battistini S; Kwieciński H; Zekanowski C
    Amyotroph Lateral Scler; 2012 Jan; 13(1):132-6. PubMed ID: 21877919
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene.
    Hermann A; Reuner U; Ziethe G; Bräuer A; Gölnitz U; Rolfs A; Ricci C
    Amyotroph Lateral Scler; 2011 Sep; 12(5):382-4. PubMed ID: 21413851
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.