BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 22647583)

  • 1. Distinctive clinicopathological features of 2 large families with amyotrophic lateral sclerosis having L106V mutation in SOD1 gene.
    Hineno A; Nakamura A; Shimojima Y; Yoshida K; Oyanagai K; Ikeda S
    J Neurol Sci; 2012 Aug; 319(1-2):63-74. PubMed ID: 22647583
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1: gene multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes.
    Kato S; Shimoda M; Watanabe Y; Nakashima K; Takahashi K; Ohama E
    J Neuropathol Exp Neurol; 1996 Oct; 55(10):1089-101. PubMed ID: 8858006
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions.
    Kato S; Saito M; Hirano A; Ohama E
    Histol Histopathol; 1999 Jul; 14(3):973-89. PubMed ID: 10425565
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.
    Kato S; Sumi-Akamaru H; Fujimura H; Sakoda S; Kato M; Hirano A; Takikawa M; Ohama E
    Acta Neuropathol; 2001 Sep; 102(3):233-8. PubMed ID: 11585247
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 14-3-3 proteins in Lewy body-like hyaline inclusions in a patient with familial amyotrophic lateral sclerosis with a two-base pair deletion in the Cu/Zn superoxide dismutase (SOD1) gene.
    Kawamoto Y; Akiguchi I; Fujimura H; Shirakashi Y; Honjo Y; Sakoda S
    Acta Neuropathol; 2005 Aug; 110(2):203-4. PubMed ID: 15973542
    [No Abstract]   [Full Text] [Related]  

  • 9. Familial amyotrophic lateral sclerosis with Cys111Tyr mutation in Cu/Zn superoxide dismutase showing widespread Lewy body-like hyaline inclusions.
    Suzuki M; Yasui K; Ishikawai H; Nomura M; Watanabe T; Mikami H; Yamano T; Ono S
    J Neurol Sci; 2011 Jan; 300(1-2):182-4. PubMed ID: 20888599
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
    Kato S; Funakoshi H; Nakamura T; Kato M; Nakano I; Hirano A; Ohama E
    Acta Neuropathol; 2003 Aug; 106(2):112-20. PubMed ID: 12707786
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions.
    Takehisa Y; Ujike H; Ishizu H; Terada S; Haraguchi T; Tanaka Y; Nishinaka T; Nobukuni K; Ihara Y; Namba R; Yasuda T; Nishibori M; Hayabara T; Kuroda S
    Arch Neurol; 2001 May; 58(5):736-40. PubMed ID: 11346368
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis.
    Kawamoto Y; Ito H; Kobayashi Y; Suzuki Y; Akiguchi I; Fujimura H; Sakoda S; Kusaka H; Hirano A; Takahashi R
    Neuropathol Appl Neurobiol; 2010 Jun; 36(4):331-44. PubMed ID: 20202124
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation.
    Kokubo Y; Kuzuhara S; Narita Y; Kikugawa K; Nakano R; Inuzuka T; Tsuji S; Watanabe M; Miyazaki T; Murayama S; Ihara Y
    Arch Neurol; 1999 Dec; 56(12):1506-8. PubMed ID: 10593307
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [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]  

  • 17. Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase.
    Ohi T; Saita K; Takechi S; Nabesima K; Tashiro H; Shiomi K; Sugimoto S; Akematsu T; Nakayama T; Iwaki T; Matsukura S
    J Neurol Sci; 2002 May; 197(1-2):73-8. PubMed ID: 11997070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.
    Ince PG; Tomkins J; Slade JY; Thatcher NM; Shaw PJ
    J Neuropathol Exp Neurol; 1998 Oct; 57(10):895-904. PubMed ID: 9786240
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial amyotrophic lateral sclerosis: a SOD1-unrelated Japanese family of bulbar type with Bunina bodies and ubiquitin-positive skein-like inclusions in lower motor neurons.
    Tagawa A; Tan CF; Kikugawa K; Fukase M; Nakano R; Onodera O; Nishizawa M; Takahashi H
    Acta Neuropathol; 2007 Feb; 113(2):205-11. PubMed ID: 17036243
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 10.