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 *

392 related articles for article (PubMed ID: 26719496)

  • 1. Alexander Disease: A Novel Mutation in GFAP Leading to Epilepsia Partialis Continua.
    Bonthius DJ; Karacay B
    J Child Neurol; 2016 Jun; 31(7):869-72. PubMed ID: 26719496
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel deletion mutation in GFAP gene in an infantile form of Alexander disease.
    Murakami N; Tsuchiya T; Kanazawa N; Tsujino S; Nagai T
    Pediatr Neurol; 2008 Jan; 38(1):50-2. PubMed ID: 18054694
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Whole Exon Deletion in the GFAP Gene Is a Novel Molecular Mechanism Causing Alexander Disease.
    Green L; Berry IR; Childs AM; McCullagh H; Jose S; Warren D; Craven I; Camm N; Prescott K; van der Knaap MS; Sheridan E; Livingston JH
    Neuropediatrics; 2018 Apr; 49(2):118-122. PubMed ID: 29253910
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases.
    Knuutinen O; Kousi M; Suo-Palosaari M; Moilanen JS; Tuominen H; Vainionpää L; Joensuu T; Anttonen AK; Uusimaa J; Lehesjoki AE; Vieira P
    Neuropediatrics; 2018 Aug; 49(4):256-261. PubMed ID: 29801191
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P.
    Suzuki Y; Kanazawa N; Takenaka J; Okumura A; Negoro T; Tsujino S
    Brain Dev; 2004 Apr; 26(3):206-8. PubMed ID: 15030911
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An unusual presentation of late-onset Alexander's disease with slow orthostatic tremor and a novel GFAP variant.
    Stitt DW; Gavrilova R; Watson R; Hassan A
    Neurocase; 2018; 24(5-6):266-268. PubMed ID: 30755139
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and genetic study in Chinese patients with Alexander disease.
    Ye Wu ; Qiang Gu ; Jingmin Wang ; Yanling Yang ; Xiru Wu ; Yuwu Jiang
    J Child Neurol; 2008 Feb; 23(2):173-7. PubMed ID: 18079314
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Alexander disease.
    Messing A
    Handb Clin Neurol; 2018; 148():693-700. PubMed ID: 29478608
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis.
    Brackmann F; Coras R; Rössler K; Kraus C; Rompel O; Trollmann R
    Brain Dev; 2018 Apr; 40(4):330-333. PubMed ID: 29191363
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case of severe Alexander disease with de novo c. 239 T > C, p.(F80S), in GFAP.
    Matsumoto A; Tulyeu J; Furukawa R; Watanabe C; Monden Y; Nozaki Y; Mori M; Namekawa M; Jimbo EF; Aihara T; Yamagata T; Osaka H
    Brain Dev; 2018 Aug; 40(7):587-591. PubMed ID: 29573842
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aggregation-prone GFAP mutation in Alexander disease validated using a zebrafish model.
    Lee SH; Nam TS; Kim KH; Kim JH; Yoon W; Heo SH; Kim MJ; Shin BA; Perng MD; Choy HE; Jo J; Kim MK; Choi SY
    BMC Neurol; 2017 Sep; 17(1):175. PubMed ID: 28882119
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander disease.
    Bachetti T; Caroli F; Bocca P; Prigione I; Balbi P; Biancheri R; Filocamo M; Mariotti C; Pareyson D; Ravazzolo R; Ceccherini I
    Eur J Hum Genet; 2008 Apr; 16(4):462-70. PubMed ID: 18197187
    [TBL] [Abstract][Full Text] [Related]  

  • 14. GFAP mutations in Alexander disease.
    Li R; Messing A; Goldman JE; Brenner M
    Int J Dev Neurosci; 2002; 20(3-5):259-68. PubMed ID: 12175861
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Murine model of Alexander disease: analysis of GFAP aggregate formation and its pathological significance.
    Tanaka KF; Takebayashi H; Yamazaki Y; Ono K; Naruse M; Iwasato T; Itohara S; Kato H; Ikenaka K
    Glia; 2007 Apr; 55(6):617-31. PubMed ID: 17299771
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients.
    Meins M; Brockmann K; Yadav S; Haupt M; Sperner J; Stephani U; Hanefeld F
    Neuropediatrics; 2002 Aug; 33(4):194-8. PubMed ID: 12368989
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aggregate formation analysis of GFAP
    Tulyeu J; Tamaura M; Jimbo E; Shimbo H; Takano K; Iai M; Yamashita S; Goto T; Aida N; Tokuhiro E; Yamagata T; Osaka H
    Brain Dev; 2019 Feb; 41(2):195-200. PubMed ID: 30213442
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Identification of a novel nonsense mutation in the rod domain of GFAP that is associated with Alexander disease.
    Nam TS; Kim JH; Chang CH; Yoon W; Jung YS; Kang SY; Shin BA; Perng MD; Choi SY; Kim MK
    Eur J Hum Genet; 2015 Jan; 23(1):72-8. PubMed ID: 24755947
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Review of Alexander disease: beyond the classical concept of leukodystrophy.
    Sawaishi Y
    Brain Dev; 2009 Aug; 31(7):493-8. PubMed ID: 19386454
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.