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 *

148 related articles for article (PubMed ID: 22619055)

  • 1. Adult-onset Alexander disease with an R66Q mutation in GFAP presented with severe vocal cord paralysis during sleep.
    Hida A; Ishiura H; Arai N; Fukuoka H; Hasuo K; Goto J; Uesaka Y; Tsuji S; Takeuchi S
    J Neurol; 2012 Oct; 259(10):2234-6. PubMed ID: 22619055
    [No Abstract]   [Full Text] [Related]  

  • 2. Late onset Alexander's disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP gene.
    Schmidt S; Wattjes MP; Gerding WM; van der Knaap M
    J Neurol; 2011 May; 258(5):938-40. PubMed ID: 21165639
    [No Abstract]   [Full Text] [Related]  

  • 3. Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature.
    Pareyson D; Fancellu R; Mariotti C; Romano S; Salmaggi A; Carella F; Girotti F; Gattellaro G; Carriero MR; Farina L; Ceccherini I; Savoiardo M
    Brain; 2008 Sep; 131(Pt 9):2321-31. PubMed ID: 18684770
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dominantly-inherited adult-onset leukodystrophy with palatal tremor caused by a mutation in the glial fibrillary acidic protein gene.
    Thyagarajan D; Chataway T; Li R; Gai WP; Brenner M
    Mov Disord; 2004 Oct; 19(10):1244-8. PubMed ID: 15390001
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial adult-onset Alexander disease with a novel mutation (D78N) in the glial fibrillary acidic protein gene with unusual bilateral basal ganglia involvement.
    Wada Y; Yanagihara C; Nishimura Y; Namekawa M
    J Neurol Sci; 2013 Aug; 331(1-2):161-4. PubMed ID: 23743246
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel GFAP mutation in patient with adult-onset Alexander disease presenting with spastic ataxia.
    Kaneko H; Hirose M; Katada S; Takahashi T; Naruse S; Tsuchiya M; Yoshida T; Nakagawa M; Onodera O; Nishizawa M; Ikeuchi T
    Mov Disord; 2009 Jul; 24(9):1393-5. PubMed ID: 19412928
    [No Abstract]   [Full Text] [Related]  

  • 7. Parkinsonism phenotype in a family with adult onset Alexander disease and a novel mutation of GFAP.
    Vázquez-Justes D; Peñalva-García J; López R; Mitjana R; Begue R; González-Mingot C
    Clin Neurol Neurosurg; 2020 Aug; 195():105893. PubMed ID: 32417628
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel mutation in the GFAP gene in a familial adult onset Alexander disease.
    Salmaggi A; Botturi A; Lamperti E; Grisoli M; Fischetto R; Ceccherini I; Caroli F; Boiardi A
    J Neurol; 2007 Sep; 254(9):1278-80. PubMed ID: 17703343
    [No Abstract]   [Full Text] [Related]  

  • 9. Type II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene.
    Chang KE; Pratt D; Mishra BB; Edwards N; Hallett M; Ray-Chaudhury A
    Clin Neuropathol; 2015; 34(5):298-302. PubMed ID: 25997626
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GFAP canonical transcript may not be suitable for the diagnosis of adult-onset Alexander disease.
    Pinto E Vairo F; Bertsch N; Klee EW; Gavrilova RH
    Acta Neuropathol Commun; 2018 Oct; 6(1):112. PubMed ID: 30355306
    [No Abstract]   [Full Text] [Related]  

  • 11. Long-term follow-up of a case of adult-onset Alexander disease presenting with cognitive impairment as the initial symptom.
    Kawai Y; Hattori M; Mori K; Ieda T
    Neurol India; 2017; 65(4):887-889. PubMed ID: 28681773
    [No Abstract]   [Full Text] [Related]  

  • 12. [Glial fibrillary acidic protein mutation in a Chinese girl with infantile Alexander disease].
    Ma HW; Lu JF; Jiang J; Chen LY; Niu GH; Wu BM; Kanazawa N; Tsujino S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):79-81. PubMed ID: 15696488
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.
    Yoshida T; Sasayama H; Mizuta I; Okamoto Y; Yoshida M; Riku Y; Hayashi Y; Yonezu T; Takata Y; Ohnari K; Okuda S; Aiba I; Nakagawa M
    Acta Neurol Scand; 2011 Aug; 124(2):104-8. PubMed ID: 20849398
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case of Alexander disease with dropped head syndrome].
    Maeda K; Iwai K; Kobayashi Y; Tsuji H; Yoshida T; Kobayashi Y
    Rinsho Shinkeigaku; 2018 Mar; 58(3):198-201. PubMed ID: 29491332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Adult onset Alexander disease presenting with progressive spastic paraplegia.
    Pedroso JL; Raskin S; Barsottini OG; Oliveira AS
    Parkinsonism Relat Disord; 2014 Feb; 20(2):241-2. PubMed ID: 24188966
    [No Abstract]   [Full Text] [Related]  

  • 16. A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutation.
    Kinoshita T; Imaizumi T; Miura Y; Fujimoto H; Ayabe M; Shoji H; Okamoto Y; Takashima H; Osame M; Nakagawa M
    Neurosci Lett; 2003 Oct; 350(3):169-72. PubMed ID: 14550921
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acute onset of adult Alexander disease.
    Schmidt H; Kretzschmar B; Lingor P; Pauli S; Schramm P; Otto M; Ohlenbusch A; Brockmann K
    J Neurol Sci; 2013 Aug; 331(1-2):152-4. PubMed ID: 23706596
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An adult form of Alexander disease: a novel mutation in glial fibrillary acidic protein.
    Ohnari K; Yamano M; Uozumi T; Hashimoto T; Tsuji S; Nakagawa M
    J Neurol; 2007 Oct; 254(10):1390-4. PubMed ID: 17934883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation in the
    Casasnovas C; Verdura E; Vélez V; Schlüter A; Pons-Escoda A; Homedes C; Ruiz M; Fourcade S; Launay N; Pujol A
    J Med Genet; 2019 Dec; 56(12):846-849. PubMed ID: 31004048
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Alexander disease with periventricular calcification: a novel mutation of the GFAP gene.
    Jefferson RJ; Absoud M; Jain R; Livingston JH; VAN DER Knaap MS; Jayawant S
    Dev Med Child Neurol; 2010 Dec; 52(12):1160-3. PubMed ID: 20964669
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.