216 related articles for article (PubMed ID: 21233330)
1. A Rosenthal fiber encephalomyelopathy resembling Alexander's disease in 3 sheep.
Kessell AE; Finnie JW; Manavis J; Cheetham GD; Blumbergs PC
Vet Pathol; 2012 Mar; 49(2):248-54. PubMed ID: 21233330
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. 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. PubMed ID: 23594359
[TBL] [Abstract][Full Text] [Related]
5. The clinicopathological spectrum of Rosenthal fibre encephalopathy and Alexander's disease: a case report and review of the literature.
Jacob J; Robertson NJ; Hilton DA
J Neurol Neurosurg Psychiatry; 2003 Jun; 74(6):807-10. PubMed ID: 12754360
[TBL] [Abstract][Full Text] [Related]
6. The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27.
Der Perng M; Su M; Wen SF; Li R; Gibbon T; Prescott AR; Brenner M; Quinlan RA
Am J Hum Genet; 2006 Aug; 79(2):197-213. PubMed ID: 16826512
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Clinical aspects and pathology of Alexander disease, and morphological and functional alteration of astrocytes induced by GFAP mutation.
Yoshida T; Nakagawa M
Neuropathology; 2012 Aug; 32(4):440-6. PubMed ID: 22118268
[TBL] [Abstract][Full Text] [Related]
9. Rosenthal fiber encephalopathy in a dog resembling Alexander disease in humans.
Alemañ N; Marcaccini A; Espino L; Bermúdez R; Nieto JM; López-Peña M
Vet Pathol; 2006 Nov; 43(6):1025-8. PubMed ID: 17099166
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The origin of Rosenthal fibers and their contributions to astrocyte pathology in Alexander disease.
Sosunov AA; McKhann GM; Goldman JE
Acta Neuropathol Commun; 2017 Mar; 5(1):27. PubMed ID: 28359321
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Alexander's disease: clinical, pathologic, and genetic features.
Johnson AB; Brenner M
J Child Neurol; 2003 Sep; 18(9):625-32. PubMed ID: 14572141
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Generation of mice with glial cell dysfunction].
Tanaka K; Lee HU; Ikenaka K
Brain Nerve; 2007 Jul; 59(7):747-53. PubMed ID: 17663146
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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; 18(7):1190-9. PubMed ID: 19129171
[TBL] [Abstract][Full Text] [Related]
18. Alexander disease-associated glial fibrillary acidic protein mutations in mice induce Rosenthal fiber formation and a white matter stress response.
Hagemann TL; Connor JX; Messing A
J Neurosci; 2006 Oct; 26(43):11162-73. PubMed ID: 17065456
[TBL] [Abstract][Full Text] [Related]
19. Fibrinoid leukodystrophy (Alexander's disease-like disorder) in a young adult French bulldog.
Ito T; Uchida K; Nakamura M; Nakashima K; Suzuki K; Nakayama H
J Vet Med Sci; 2010 Oct; 72(10):1387-90. PubMed ID: 20526046
[TBL] [Abstract][Full Text] [Related]
20. Astrocytes cultured from transgenic mice carrying the added human glial fibrillary acidic protein gene contain Rosenthal fibers.
Eng LF; Lee YL; Kwan H; Brenner M; Messing A
J Neurosci Res; 1998 Aug; 53(3):353-60. PubMed ID: 9698163
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]