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Items: 1 to 20 of 139

1.

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 15;331(1-2):152-4. doi: 10.1016/j.jns.2013.05.006. Epub 2013 May 23.

PMID:
23706596
2.

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 15;331(1-2):161-4. doi: 10.1016/j.jns.2013.05.019. Epub 2013 Jun 4.

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. doi: 10.1093/brain/awn178. Epub 2008 Aug 6. Review.

4.

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. doi: 10.1111/j.1600-0404.2010.01427.x. Epub 2010 Sep 16.

PMID:
20849398
5.

Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature.

Namekawa M, Takiyama Y, Honda J, Shimazaki H, Sakoe K, Nakano I.

BMC Neurol. 2010 Apr 1;10:21. doi: 10.1186/1471-2377-10-21. Review.

6.

[Adult onset Alexander disease with a novel variant (S398F) in the glial fibrillary acidic protein gene].

Sueda Y, Takahashi T, Ochi K, Ohtsuki T, Namekawa M, Kohriyama T, Takiyama Y, Matsumoto M.

Rinsho Shinkeigaku. 2009 Jun;49(6):358-63. Review. Japanese.

PMID:
19618846
7.

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.

PMID:
12975300
8.

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. Epub 2007 Oct 15.

PMID:
17934883
9.

Adult-onset Alexander disease : report on a family.

Balbi P, Seri M, Ceccherini I, Uggetti C, Casale R, Fundarò C, Caroli F, Santoro L.

J Neurol. 2008 Jan;255(1):24-30. Epub 2007 Nov 21.

PMID:
18004641
10.

An unusual presentation of juvenile Alexander disease.

Osorio MJ, Risen S, Alper G.

J Child Neurol. 2012 Apr;27(4):507-10. doi: 10.1177/0883073811419263. Epub 2011 Sep 21.

PMID:
21940697
11.

A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?

Brockmann K, Meins M, Taubert A, Trappe R, Grond M, Hanefeld F.

Eur Neurol. 2003;50(2):100-5.

PMID:
12944715
12.

Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.

van der Knaap MS, Ramesh V, Schiffmann R, Blaser S, Kyllerman M, Gholkar A, Ellison DW, van der Voorn JP, van Dooren SJ, Jakobs C, Barkhof F, Salomons GS.

Neurology. 2006 Feb 28;66(4):494-8.

PMID:
16505300
13.

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 30;350(3):169-72.

PMID:
14550921
14.

Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder.

Nishri D, Edvardson S, Lev D, Leshinsky-Silver E, Ben-Sira L, Henneke M, Lerman-Sagie T, Blumkin L.

Eur J Paediatr Neurol. 2014 Jul;18(4):495-501. doi: 10.1016/j.ejpn.2014.03.009. Epub 2014 Apr 8.

PMID:
24742911
15.

Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortex.

Suzuki H, Yoshida T, Kitada M, Ichihashi J, Sasayama H, Nishikawa Y, Mistui Y, Nakagawa M, Kusunoki S.

J Neurol. 2012 Mar;259(3):457-61. doi: 10.1007/s00415-011-6201-z. Epub 2011 Aug 7.

PMID:
21822933
16.

An autopsied case of adult-onset bulbospinalform Alexander disease with a novel S393R mutation in the GFAP gene.

Iwasaki Y, Saito Y, Mori K, Ito M, Mimuro M, Aiba I, Saito K, Mizuta I, Yoshida T, Nakagawa M, Yoshida M.

Clin Neuropathol. 2015 Jul-Aug;34(4):207-14. doi: 10.5414/NP300806.

PMID:
25828773
17.

Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis.

Yoshida T, Sasaki M, Yoshida M, Namekawa M, Okamoto Y, Tsujino S, Sasayama H, Mizuta I, Nakagawa M; Alexander Disease Study Group in Japan.

J Neurol. 2011 Nov;258(11):1998-2008. doi: 10.1007/s00415-011-6056-3. Epub 2011 May 1.

PMID:
21533827
18.

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. doi: 10.1111/j.1469-8749.2010.03784.x. Epub 2010 Oct 21.

19.

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. Epub 2007 Mar 23.

PMID:
17383133
20.

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
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