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Items: 1 to 20 of 89

1.

Alexander disease.

Messing A, Brenner M, Feany MB, Nedergaard M, Goldman JE.

J Neurosci. 2012 Apr 11;32(15):5017-23. doi: 10.1523/JNEUROSCI.5384-11.2012. No abstract available.

2.

Alexander disease: GFAP mutations unify young and old.

Messing A, Brenner M.

Lancet Neurol. 2003 Feb;2(2):75. No abstract available.

PMID:
12849260
3.

Alexander disease and megalencephalic leukoencephalopathy with subcortical cysts: leukodystrophies arising from astrocyte dysfunction.

Gorospe JR, Maletkovic J.

Ment Retard Dev Disabil Res Rev. 2006;12(2):113-22. Review. No abstract available.

PMID:
16807904
4.

[Glial fibrillary acidic protein: the component of intermediate filaments in the vertebrate brain astrocytes].

Sukhorukova EG, Kruzhevskiĭ DÉ, Alekseeva OS.

Zh Evol Biokhim Fiziol. 2015 Jan-Feb;51(1):3-10. Review. Russian.

PMID:
25859599
5.

Alexander disease: a review and the gene.

Johnson AB.

Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):391-4. Review.

PMID:
12175878
6.

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.

PMID:
15732097
7.

Alexander disease with occipital predominance and a novel c.799G>C mutation in the GFAP gene.

Hinttala R, Karttunen V, Karttunen A, Herva R, Uusimaa J, Remes AM.

Acta Neuropathol. 2007 Nov;114(5):543-5. Epub 2007 Sep 6. No abstract available.

PMID:
17805552
8.

A novel GFAP mutation in a type II (late-onset) Alexander disease patient.

de Paiva AR, Freua F, Lucato LT, Parmera J, Dória D, Nóbrega PR, Olávio TR, Macedo-Souza LI, Kok F.

J Neurol. 2016 Apr;263(4):821-2. doi: 10.1007/s00415-016-8065-8. Epub 2016 Feb 25. No abstract available.

PMID:
26914930
9.

Alexander disease: combined gene analysis and MRI clarify pathogenesis and extend phenotype.

Moser HW.

Ann Neurol. 2005 Mar;57(3):307-8. No abstract available.

PMID:
15732119
10.

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 15;24(9):1393-5. doi: 10.1002/mds.22556. No abstract available.

PMID:
19412928
11.

Alexander disease: putative mechanisms of an astrocytic encephalopathy.

Mignot C, Boespflug-Tanguy O, Gelot A, Dautigny A, Pham-Dinh D, Rodriguez D.

Cell Mol Life Sci. 2004 Feb;61(3):369-85. Review.

PMID:
14770299
12.

Suppression of GFAP toxicity by alphaB-crystallin in mouse models of Alexander disease.

Hagemann TL, Boelens WC, Wawrousek EF, Messing A.

Hum Mol Genet. 2009 Apr 1;18(7):1190-9. doi: 10.1093/hmg/ddp013. Epub 2009 Jan 7.

13.

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 Sep-Oct;37(5):698-700. doi: 10.1097/RCT.0b013e31829f5a04.

PMID:
24045243
14.

Strategies for treatment in Alexander disease.

Messing A, LaPash Daniels CM, Hagemann TL.

Neurotherapeutics. 2010 Oct;7(4):507-15. doi: 10.1016/j.nurt.2010.05.013. Review.

15.

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. doi: 10.1007/s00415-010-5849-0. Epub 2010 Dec 17. No abstract available.

PMID:
21165639
16.

Synemin is expressed in reactive astrocytes and Rosenthal fibers in Alexander disease.

Pekny T, Faiz M, Wilhelmsson U, Curtis MA, Matej R, Skalli O, Pekny M.

APMIS. 2014 Jan;122(1):76-80. doi: 10.1111/apm.12088. Epub 2013 Apr 18.

PMID:
23594359
17.

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.

PMID:
18054694
18.

Infantile-onset Alexander disease: a genetically proven case with mild clinical course in a 6-year-old Indian boy.

Ramesh K, Sharma S, Kumar A, Salomons GS, van der Knaap MS, Gulati S.

J Child Neurol. 2013 Mar;28(3):396-8. doi: 10.1177/0883073812444313. Epub 2012 May 7.

PMID:
22566711
19.

Plectin regulates the organization of glial fibrillary acidic protein in Alexander disease.

Tian R, Gregor M, Wiche G, Goldman JE.

Am J Pathol. 2006 Mar;168(3):888-97.

20.

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. Epub 2005 Sep 15.

PMID:
16168593

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