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 *

87 related articles for article (PubMed ID: 16435343)

  • 1. Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy.
    Stewart HG; Mackenzie IR; Eisen A; Brännström T; Marklund SL; Andersen PM
    Muscle Nerve; 2006 May; 33(5):701-6. PubMed ID: 16435343
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial ALS with SOD1 mutation misdiagnosed with polyradiculopathy and myopathy.
    Zhou L; Pioro EP
    Amyotroph Lateral Scler; 2009; 10(5-6):476-8. PubMed ID: 19922143
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical phenotype of familial amyotrophic lateral sclerosis with
    Sun JM; Zhang CJ; Wang L; Bi HY
    Clin Neuropathol; 2022; 41(5):219-225. PubMed ID: 35652543
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sporadic amyotrophic lateral sclerosis and breast cancer: Hyaline conglomerate inclusions lead to identification of SOD1 mutation.
    Hays AP; Naini A; He CZ; Mitsumoto H; Rowland LP
    J Neurol Sci; 2006 Mar; 242(1-2):67-9. PubMed ID: 16423367
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation.
    Nakamura S; Wate R; Kaneko S; Ito H; Oki M; Tsuge A; Nagashima M; Asayama S; Fujita K; Nakamura M; Maruyama H; Kawakami H; Kusaka H
    Neuropathology; 2014 Feb; 34(1):58-63. PubMed ID: 23773010
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene.
    Tortelli R; Conforti FL; Cortese R; D'Errico E; Distaso E; Mazzei R; Ungaro C; Magariello A; Gambardella A; Logroscino G; Simone IL
    Neurobiol Aging; 2013 Jun; 34(6):1709.e3-5. PubMed ID: 23182243
    [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. Confirmation of the severe phenotypic effect of serine at codon 41 of the superoxide dismutase 1 gene.
    Subramony SH; Ashizawa T; Langford L; McKenna R; Avvaru B; Siddique T; Vedanarayanan V
    Muscle Nerve; 2011 Oct; 44(4):499-502. PubMed ID: 21755517
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial amyotrophic lateral sclerosis (FALS) with a novel SOD1 gene mutation: a clinicopathological study].
    Kawamata C; Morita M; Shibata N; Nakano I
    Rinsho Shinkeigaku; 2007 May; 47(5):211-6. PubMed ID: 17585602
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. FALS with Gly72Ser mutation in SOD1 gene: report of a family including the first autopsy case.
    Kobayashi Z; Tsuchiya K; Kubodera T; Shibata N; Arai T; Miura H; Ishikawa C; Kondo H; Ishizu H; Akiyama H; Mizusawa H
    J Neurol Sci; 2011 Jan; 300(1-2):9-13. PubMed ID: 21084099
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene.
    Battistini S; Ricci C; Lotti EM; Benigni M; Gagliardi S; Zucco R; Bondavalli M; Marcello N; Ceroni M; Cereda C
    J Neurol Sci; 2010 Jun; 293(1-2):112-5. PubMed ID: 20385392
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amyotrophic lateral sclerosis with mutation of the Cu/Zn superoxide dismutase gene (SOD1) in a patient with Down syndrome.
    Marucci G; Morandi L; Bartolomei I; Salvi F; Pession A; Righi A; Lauria G; Foschini MP
    Neuromuscul Disord; 2007 Oct; 17(9-10):673-6. PubMed ID: 17624778
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel SOD1 N86K mutation is associated with a severe phenotype in familial ALS.
    Beck M; Sendtner M; Toyka KV
    Muscle Nerve; 2007 Jul; 36(1):111-4. PubMed ID: 17299743
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with an H43R mutation in Cu/Zn superoxide dismutase].
    Mochizuki Y; Mizutani T; Nakano R; Fukushima T; Honma T; Nemoto N; Takei K
    Rinsho Shinkeigaku; 2003 Aug; 43(8):491-5. PubMed ID: 14658402
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial amyotrophic lateral sclerosis with bulbar onset and a novel Asp101Tyr Cu/Zn superoxide dismutase gene mutation.
    Tan CF; Piao YS; Hayashi S; Obata H; Umeda Y; Sato M; Fukushima T; Nakano R; Tsuji S; Takahashi H
    Acta Neuropathol; 2004 Oct; 108(4):332-6. PubMed ID: 15235802
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Development of diabetes in a familial amyotrophic lateral sclerosis patient carrying the I113T SOD1 mutation. Case Report.
    Hamasaki H; Takeuchi Y; Masui Y; Ohta Y; Abe K; Yoshino H; Yanai H
    Neuro Endocrinol Lett; 2015; 36(5):414-6. PubMed ID: 26707039
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.