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 *

188 related articles for article (PubMed ID: 20235485)

  • 1. [Two cases of familial amyotrophic lateral sclerosis with a SOD1L126S mutation showing high age at onset and slow progression].
    Iwashima T; Tateishi T; Yamasaki R; Motomura K; Ohyagi Y; Kira J
    Rinsho Shinkeigaku; 2010 Mar; 50(3):163-7. PubMed ID: 20235485
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Neurological CPC.57. An 80-year-old woman with four years history of muscle atrophy involving lower extremities predominantly on the right side].
    Miwa H; Mori H; Sumino S; Matsuoka S; Shirai T; Imai H; Mizuno Y
    No To Shinkei; 1997 Sep; 49(9):857-65. PubMed ID: 9311007
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Different clinical phenotypes of siblings with familial amyotrophic lateral sclerosis showing Cys146Arg point mutation of superoxide dismutase 1 gene].
    Ito K; Uchiyama T; Fukutake T; Arai K; Kanesaka T; Hattori T
    Rinsho Shinkeigaku; 2002 Feb; 42(2):175-7. PubMed ID: 12424972
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A patient with motor neuron syndrome clinically similar to amyotrophic lateral sclerosis, presenting spontaneous recovery].
    Miyoshi K; Ohyagi Y; Amano T; Inoue I; Miyoshi S; Tsuji S; Yamada T; Kira J
    Rinsho Shinkeigaku; 2000 Nov; 40(11):1090-5. PubMed ID: 11332188
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations.
    Abe K; Aoki M; Ikeda M; Watanabe M; Hirai S; Itoyama Y
    J Neurol Sci; 1996 Mar; 136(1-2):108-16. PubMed ID: 8815157
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS.
    Aoki M; Ogasawara M; Matsubara Y; Narisawa K; Nakamura S; Itoyama Y; Abe K
    J Neurol Sci; 1994 Oct; 126(1):77-83. PubMed ID: 7836951
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation.
    Lopate G; Baloh RH; Al-Lozi MT; Miller TM; Fernandes Filho JA; Ni O; Leston A; Florence J; Schierbecker J; Allred P
    Amyotroph Lateral Scler; 2010; 11(1-2):232-6. PubMed ID: 20184521
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [A 49-year-old man with progressive bulbar palsy and respiratory failure].
    Motoi Y; Satoh K; Matsumine H; Wakiya M; Mori H; Shirai T; Kondo T; Mizuno Y
    No To Shinkei; 1998 Jan; 50(1):93-100. PubMed ID: 9493205
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Amyotrophic lateral sclerosis.
    Wijesekera LC; Leigh PN
    Orphanet J Rare Dis; 2009 Feb; 4():3. PubMed ID: 19192301
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS).
    Cervenakova L; Protas II; Hirano A; Votiakov VI; Nedzved MK; Kolomiets ND; Taller I; Park KY; Sambuughin N; Gajdusek DC; Brown P; Goldfarb LG
    J Neurol Sci; 2000 Aug; 177(2):124-30. PubMed ID: 10980308
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. [Familial amyotrophic lateral sclerosis with rapid progression].
    Oyama G; Izawa N; Fujishima K; Kobayashi H; Mizuno Y; Okuma Y
    No To Shinkei; 2005 Nov; 57(11):1003-6. PubMed ID: 16363640
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [The diagnosis of amyotrophic lateral sclerosis supported by motor evoked potential and brain MRI studies].
    Matsunaga K; Iwamoto M; Tsuji S; Hashimoto T; Murai Y
    Rinsho Shinkeigaku; 1997 Mar; 37(3):233-8. PubMed ID: 9217423
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Facial onset amyotrophic lateral sclerosis with K3E variant in the Cu/Zn superoxide dismutase gene.
    Shibuya K; Sawai S; Sugiyama A; Koide M; Nishiyama A; Aoki M; Kuwabara S
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):144-146. PubMed ID: 32729725
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.