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 *

181 related articles for article (PubMed ID: 12497239)

  • 1. Alexander's disease in a neurologically normal child: a case report.
    Guthrie SO; Burton EM; Knowles P; Marshall R
    Pediatr Radiol; 2003 Jan; 33(1):47-9. PubMed ID: 12497239
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP.
    Shiihara T; Sawaishi Y; Adachi M; Kato M; Hayasaka K
    J Neurol Sci; 2004 Oct; 225(1-2):125-7. PubMed ID: 15465095
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Atypical focal MRI lesions in a case of juvenile Alexander's disease.
    Probst EN; Hagel C; Weisz V; Nagel S; Wittkugel O; Zeumer H; Kohlschütter A
    Ann Neurol; 2003 Jan; 53(1):118-20. PubMed ID: 12509855
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unusual variants of Alexander's disease.
    van der Knaap MS; Salomons GS; Li R; Franzoni E; Gutiérrez-Solana LG; Smit LM; Robinson R; Ferrie CD; Cree B; Reddy A; Thomas N; Banwell B; Barkhof F; Jakobs C; Johnson A; Messing A; Brenner M
    Ann Neurol; 2005 Mar; 57(3):327-38. PubMed ID: 15732098
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease.
    Namekawa M; Takiyama Y; Aoki Y; Takayashiki N; Sakoe K; Shimazaki H; Taguchi T; Tanaka Y; Nishizawa M; Saito K; Matsubara Y; Nakano I
    Ann Neurol; 2002 Dec; 52(6):779-85. PubMed ID: 12447932
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Juvenile form of Alexander's disease - a case confirmed by detection of mutation in GFAP gene].
    Kmieć T; Bilska M; Mierzewska H; Jurkiewicz E; Jóźwiak S
    Neurol Neurochir Pol; 2007; 41(3):267-71. PubMed ID: 17629821
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluctuation of computed tomographic findings in white matter in Alexander's disease.
    Shiihara T; Kato M; Honma T; Ohtaki S; Sawaishi Y; Hayasaka K
    J Child Neurol; 2002 Mar; 17(3):227-30. PubMed ID: 12026242
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis.
    Sakakibara T; Takahashi Y; Fukuda K; Inoue T; Kurosawa T; Nishikubo T; Shima M; Taoka T; Aida N; Tsujino S; Kanazawa N; Yoshioka A
    Brain Dev; 2007 Sep; 29(8):525-8. PubMed ID: 17383133
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.
    Asahina N; Okamoto T; Sudo A; Kanazawa N; Tsujino S; Saitoh S
    Brain Dev; 2006 Mar; 28(2):131-3. PubMed ID: 16168593
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene.
    Stumpf E; Masson H; Duquette A; Berthelet F; McNabb J; Lortie A; Lesage J; Montplaisir J; Brais B; Cossette P
    Arch Neurol; 2003 Sep; 60(9):1307-12. PubMed ID: 12975300
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease.
    Li R; Johnson AB; Salomons G; Goldman JE; Naidu S; Quinlan R; Cree B; Ruyle SZ; Banwell B; D'Hooghe M; Siebert JR; Rolf CM; Cox H; Reddy A; Gutiérrez-Solana LG; Collins A; Weller RO; Messing A; van der Knaap MS; Brenner M
    Ann Neurol; 2005 Mar; 57(3):310-26. PubMed ID: 15732097
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Adult Alexander's disease without leukoencephalopathy.
    Salvi F; Aoki Y; Della Nave R; Vella A; Pastorelli F; Scaglione C; Matsubara Y; Mascalchi M
    Ann Neurol; 2005 Nov; 58(5):813-4. PubMed ID: 16240361
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. An unusual presentation of juvenile Alexander disease.
    Osorio MJ; Risen S; Alper G
    J Child Neurol; 2012 Apr; 27(4):507-10. PubMed ID: 21940697
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alexander disease: a novel mutation in the glial fibrillary acidic protein gene with initial uncommon clinical and magnetic resonance imaging findings.
    da Silva Pereira CC; Gattás GS; Lucato LT
    J Comput Assist Tomogr; 2013; 37(5):698-700. PubMed ID: 24045243
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Early mitochondrial dysfunction in an infant with Alexander disease.
    Cáceres-Marzal C; Vaquerizo J; Galán E; Fernández S
    Pediatr Neurol; 2006 Oct; 35(4):293-6. PubMed ID: 16996408
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.