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2. Alexander's disease: a case report with brain biopsy, ultrasound, CT scan and MRI findings. Arend AO; Leary PM; Rutherfoord GS Clin Neuropathol; 1991; 10(3):122-6. PubMed ID: 1650301 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Alpha B-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain. Iwaki T; Kume-Iwaki A; Liem RK; Goldman JE Cell; 1989 Apr; 57(1):71-8. PubMed ID: 2539261 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Alpha A-crystallin and alpha B-crystallin, newly identified interaction proteins of protease-activated receptor-2, rescue astrocytes from C2-ceramide- and staurosporine-induced cell death. Li R; Rohatgi T; Hanck T; Reiser G J Neurochem; 2009 Sep; 110(5):1433-44. PubMed ID: 19558454 [TBL] [Abstract][Full Text] [Related]
7. Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold. Tomokane N; Iwaki T; Tateishi J; Iwaki A; Goldman JE Am J Pathol; 1991 Apr; 138(4):875-85. PubMed ID: 1707236 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Alexander's disease: a case report of a biopsy proven case. Tatke M; Sharma A Neurol India; 1999 Dec; 47(4):333-5. PubMed ID: 10625914 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Reinduced expression of developmental proteins (nestin, small heat shock protein) in and around cerebral arteriovenous malformations. Ha Y; Kim TS; Yoon DH; Cho YE; Huh SG; Lee KC Clin Neuropathol; 2003; 22(5):252-61. PubMed ID: 14531551 [TBL] [Abstract][Full Text] [Related]
13. Alexander disease: a case report and review of the literature. Reichard EA; Ball WS; Bove KE Pediatr Pathol Lab Med; 1996; 16(2):327-43. PubMed ID: 9025838 [TBL] [Abstract][Full Text] [Related]
14. Interactions of GFAP with ceftriaxone and phenytoin: SRCD and molecular docking and dynamic simulation. Ruzza P; Vitale RM; Hussain R; Biondi B; Amodeo P; Sechi G; Siligardi G Biochim Biophys Acta; 2016 Oct; 1860(10):2239-48. PubMed ID: 27133445 [TBL] [Abstract][Full Text] [Related]
15. Up-regulation of osteopontin and alphaBeta-crystallin in the normal-appearing white matter of multiple sclerosis: an immunohistochemical study utilizing tissue microarrays. Sinclair C; Mirakhur M; Kirk J; Farrell M; McQuaid S Neuropathol Appl Neurobiol; 2005 Jun; 31(3):292-303. PubMed ID: 15885066 [TBL] [Abstract][Full Text] [Related]
16. Effects of divalent metal ions on the alphaB-crystallin chaperone-like activity: spectroscopic evidence for a complex between copper(II) and protein. Ganadu ML; Aru M; Mura GM; Coi A; Mlynarz P; Kozlowski H J Inorg Biochem; 2004 Jun; 98(6):1103-9. PubMed ID: 15149821 [TBL] [Abstract][Full Text] [Related]
17. Class III beta-tubulin is constitutively coexpressed with glial fibrillary acidic protein and nestin in midgestational human fetal astrocytes: implications for phenotypic identity. Dráberová E; Del Valle L; Gordon J; Marková V; Smejkalová B; Bertrand L; de Chadarévian JP; Agamanolis DP; Legido A; Khalili K; Dráber P; Katsetos CD J Neuropathol Exp Neurol; 2008 Apr; 67(4):341-54. PubMed ID: 18379434 [TBL] [Abstract][Full Text] [Related]
18. Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies. Ferrer I; Hernández I; Boada M; Llorente A; Rey MJ; Cardozo A; Ezquerra M; Puig B Acta Neuropathol; 2003 Nov; 106(5):419-35. PubMed ID: 12955398 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Alexander disease and intermediate filaments in astrocytes: a fatal gain of function. Jaeken J Eur J Paediatr Neurol; 2001; 5(4):151-3. PubMed ID: 11587378 [No Abstract] [Full Text] [Related] [Next] [New Search]