-
1
-
-
0035163913
-
Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease
-
Brenner M, Johnson AB, Boespflug-Tanguy O, Rodriguez D, Goldman JE, Messing A. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease. Nat Genet 2001; 27: 117-20.
-
(2001)
Nat Genet
, vol.27
, pp. 117-120
-
-
Brenner, M.1
Johnson, A.B.2
Boespflug-Tanguy, O.3
Rodriguez, D.4
Goldman, J.E.5
Messing, A.6
-
2
-
-
0000879584
-
Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant
-
Alexander WS. Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant. Brain 1949; 72: 373-81.
-
(1949)
Brain
, vol.72
, pp. 373-381
-
-
Alexander, W.S.1
-
3
-
-
33750249403
-
A case of Alexander's disease
-
Jeon HJ, Lee BH, Hwang SH, Hwang YS, Chi JG. A case of Alexander's disease. J Korean Child Neurol Soc 1993; 1: 173-8.
-
(1993)
J Korean Child Neurol Soc
, vol.1
, pp. 173-178
-
-
Jeon, H.J.1
Lee, B.H.2
Hwang, S.H.3
Hwang, Y.S.4
Chi, J.G.5
-
4
-
-
0344875982
-
Alexander's disease
-
Gordon N. Alexander's disease. Eur J Paediatr Neurol 2003; 7: 395-9.
-
(2003)
Eur J Paediatr Neurol
, vol.7
, pp. 395-399
-
-
Gordon, N.1
-
5
-
-
3142748164
-
Alexander's disease: A leukodystrophy caused by a mutation in GFAP
-
Johnson AB. Alexander's disease: a leukodystrophy caused by a mutation in GFAP. Neurochem Res 2004; 29: 961-4.
-
(2004)
Neurochem Res
, vol.29
, pp. 961-964
-
-
Johnson, A.B.1
-
6
-
-
1842614425
-
Diagnosing "undiagnosed" leukodystrophies: The role of molecular genetics
-
Noetzel MJ. Diagnosing "undiagnosed" leukodystrophies: The role of molecular genetics. Neurology 2004; 62: 847-8.
-
(2004)
Neurology
, vol.62
, pp. 847-848
-
-
Noetzel, M.J.1
-
7
-
-
0017074881
-
Alexander's disease: A report and reappraisal
-
Russo LS, Aron A, Anderson PJ. Alexander's disease: A report and reappraisal. Neurology 1976; 26: 607-14.
-
(1976)
Neurology
, vol.26
, pp. 607-614
-
-
Russo, L.S.1
Aron, A.2
Anderson, P.J.3
-
8
-
-
0021775984
-
Alexander's disease
-
Townsend JJ, Wilson JF, Harris T, Coulter D, Fife R. Alexander's disease. Acta Neuropathol 1985; 67: 163-6.
-
(1985)
Acta Neuropathol
, vol.67
, pp. 163-166
-
-
Townsend, J.J.1
Wilson, J.F.2
Harris, T.3
Coulter, D.4
Fife, R.5
-
9
-
-
0026733382
-
Alexander's disease in infancy and childhood: A case report of two cases
-
Neal JW, Cave EM, Singhrao SK, Cole G, Wallace SJ. Alexander's disease in infancy and childhood: A case report of two cases. Acta Neuropathol 1992; 84: 322-7.
-
(1992)
Acta Neuropathol
, vol.84
, pp. 322-327
-
-
Neal, J.W.1
Cave, E.M.2
Singhrao, S.K.3
Cole, G.4
Wallace, S.J.5
-
10
-
-
0032988904
-
Infantile and juvenile presentation of Alexander's disease: A report of two cases
-
Deprez M, D'Hooghe M, Mission JP, de Leval L, Ceuterick C, Reznik M, Martin JJ. Infantile and juvenile presentation of Alexander's disease: A report of two cases. Acta Neurol Scand 1999; 99: 158-65.
-
(1999)
Acta Neurol Scand
, vol.99
, pp. 158-165
-
-
Deprez, M.1
D'Hooghe, M.2
Mission, J.P.3
De Leval, L.4
Ceuterick, C.5
Reznik, M.6
Martin, J.J.7
-
11
-
-
11144249812
-
Alexander disease: Past and present
-
Hanefeld FA. Alexander disease: past and present. Cell Mol Life Sci 2004; 61: 2750-2.
-
(2004)
Cell Mol Life Sci
, vol.61
, pp. 2750-2752
-
-
Hanefeld, F.A.1
-
12
-
-
19944413968
-
A case of long-term survival of a patient with infantile Alexander's disease diagnosed by DNA analysis
-
Wakabayashi K, Lai M, Masuko K, Yamashita S, Yamada M, Iwamoto H, Aida N, Shiroma N, Kanazawa N, Tsujino S. A case of long-term survival of a patient with infantile Alexander's disease diagnosed by DNA analysis. No To Hattatsu 2005; 37: 55-9.
-
(2005)
No To Hattatsu
, vol.37
, pp. 55-59
-
-
Wakabayashi, K.1
Lai, M.2
Masuko, K.3
Yamashita, S.4
Yamada, M.5
Iwamoto, H.6
Aida, N.7
Shiroma, N.8
Kanazawa, N.9
Tsujino, S.10
-
13
-
-
0027276701
-
Alexander's disease: Clues to diagnosis
-
Pridmore CL, Baraitser M, Harding B, Boyd SG, Kendall B, Brett EM. Alexander's disease: clues to diagnosis. J Child Neurol 1993; 8: 134-44.
-
(1993)
J Child Neurol
, vol.8
, pp. 134-144
-
-
Pridmore, C.L.1
Baraitser, M.2
Harding, B.3
Boyd, S.G.4
Kendall, B.5
Brett, E.M.6
-
15
-
-
0023881165
-
Isolation of a major protein component of Rosenthal fibers
-
Goldman JE, Corbin E. Isolation of a major protein component of Rosenthal fibers. Am J Pathol 1988; 130: 569-78.
-
(1988)
Am J Pathol
, vol.130
, pp. 569-578
-
-
Goldman, J.E.1
Corbin, E.2
-
16
-
-
0027742866
-
Alpha B-crystallin and 27-kd heat shock protein are regulated by stress conditions in the central nervous system and accumulate in Rosenthal fibers
-
Iwaki T, Iwaki A, Tateishi J, Sakaki Y, Goldman JE. Alpha B-crystallin and 27-kd heat shock protein are regulated by stress conditions in the central nervous system and accumulate in Rosenthal fibers. Am J Pathol 1993; 143: 487-95.
-
(1993)
Am J Pathol
, vol.143
, pp. 487-495
-
-
Iwaki, T.1
Iwaki, A.2
Tateishi, J.3
Sakaki, Y.4
Goldman, J.E.5
-
17
-
-
0025890235
-
Alexander's disease: A case report with brain biopsy, ultrasound, CT scan and MRI finding
-
Arend AO, Leary PM, Rutherfoord GS. Alexander's disease: a case report with brain biopsy, ultrasound, CT scan and MRI finding. Clin Neuropathol 1991; 10: 122-6.
-
(1991)
Clin Neuropathol
, vol.10
, pp. 122-126
-
-
Arend, A.O.1
Leary, P.M.2
Rutherfoord, G.S.3
-
18
-
-
0035100718
-
Alexander disease: Diagnosis with MR imaging
-
van der Knaap MS, Naidu S, Breiter SN, Blaser S, Stroink H, Springer S, Begeer JC, van Coster R, Barth PG, Thomas NH, Valk J, Powers JM. Alexander disease: Diagnosis with MR imaging. Am J Neuroradiol 2001; 22: 541-52.
-
(2001)
Am J Neuroradiol
, vol.22
, pp. 541-552
-
-
Van Der Knaap, M.S.1
Naidu, S.2
Breiter, S.N.3
Blaser, S.4
Stroink, H.5
Springer, S.6
Begeer, J.C.7
Van Coster, R.8
Barth, P.G.9
Thomas, N.H.10
Valk, J.11
Powers, J.M.12
-
20
-
-
0000441953
-
Dysmyelinogenic leukodystrophy; report of a case of a new, presumably familial type of leukodystrophy with megalobarencephaly
-
Wohlwill FJ, Bernstein J, Yakovlev PI. Dysmyelinogenic leukodystrophy; report of a case of a new, presumably familial type of leukodystrophy with megalobarencephaly. J Neuropathol Exper Neurol 1959; 18: 359-83.
-
(1959)
J Neuropathol Exper Neurol
, vol.18
, pp. 359-383
-
-
Wohlwill, F.J.1
Bernstein, J.2
Yakovlev, P.I.3
-
21
-
-
0029445919
-
Hereditary adult onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxia
-
Schwankhaus JD, Parisi JE, Gulledge WR, Chin L, Currier RD. Hereditary adult onset Alexander's disease with palatal myoclonus, spastic paraparesis, and cerebellar ataxia. Neurology 1995; 45: 2266-71.
-
(1995)
Neurology
, vol.45
, pp. 2266-2271
-
-
Schwankhaus, J.D.1
Parisi, J.E.2
Gulledge, W.R.3
Chin, L.4
Currier, R.D.5
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