X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (601) 601
Book Review (93) 93
Publication (69) 69
Book Chapter (17) 17
Newsletter (5) 5
Conference Proceeding (3) 3
Web Resource (3) 3
Reference (2) 2
Book / eBook (1) 1
Streaming Video (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (415) 415
humans (397) 397
alexander disease (235) 235
clinical neurology (204) 204
male (178) 178
glial fibrillary acidic protein - genetics (169) 169
female (164) 164
fibrillary acidic protein (162) 162
alexander disease - genetics (157) 157
neurosciences (152) 152
animals (141) 141
magnetic resonance imaging (139) 139
gfap (137) 137
alexander-disease (134) 134
mutation (115) 115
alexander disease - pathology (109) 109
astrocytes (107) 107
adult (104) 104
brain - pathology (102) 102
alpha-b-crystallin (95) 95
rosenthal fibers (92) 92
glial fibrillary acidic protein (87) 87
leukodystrophy (85) 85
alexander's disease (83) 83
child (80) 80
brain (79) 79
infant (79) 79
mutations (78) 78
glial fibrillary acidic protein - metabolism (77) 77
mice (77) 77
alexander disease - diagnosis (71) 71
pathology (67) 67
astrocytes - metabolism (66) 66
astrocytes - pathology (63) 63
diagnosis (61) 61
neurology (60) 60
pediatrics (60) 60
intermediate filament proteins (57) 57
alexander disease - metabolism (56) 56
middle aged (56) 56
biochemistry & molecular biology (55) 55
child, preschool (55) 55
cell biology (52) 52
adolescent (46) 46
age of onset (46) 46
alexanders disease (46) 46
alexander disease - physiopathology (44) 44
brain - metabolism (43) 43
nervous system (43) 43
article (42) 42
gene (41) 41
mice, transgenic (41) 41
mutation - genetics (41) 41
proteins (40) 40
analysis (38) 38
abridged index medicus (36) 36
diagnosis, differential (36) 36
genetic aspects (36) 36
alexander disease - complications (35) 35
expression (35) 35
aged (34) 34
disease models, animal (34) 34
astrocyte (33) 33
central-nervous-system (32) 32
dna mutational analysis (32) 32
genetics & heredity (31) 31
infantile (31) 31
intermediate filaments (31) 31
leukoencephalopathy (30) 30
magnetic resonance imaging - methods (30) 30
research (30) 30
transgenic mice (29) 29
medicine & public health (28) 28
nervous system diseases (28) 28
radiology, nuclear medicine & medical imaging (27) 27
spinal cord - pathology (27) 27
ataxia (26) 26
cells, cultured (26) 26
cytoskeleton (26) 26
phenotype (26) 26
alzheimers-disease (25) 25
cells (25) 25
immunohistochemistry (25) 25
protein (25) 25
mri (24) 24
neuroimaging (24) 24
palatal myoclonus (24) 24
spinal-cord (24) 24
gene mutations (23) 23
gfap mutations (23) 23
macromolecular substances (23) 23
multiple-sclerosis (23) 23
rats (23) 23
intermediate-filaments (22) 22
neurodegenerative diseases (22) 22
alpha-crystallin b chain - metabolism (21) 21
disease progression (21) 21
genetics (21) 21
neurodegeneration (21) 21
oxidative stress (21) 21
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (593) 593
Japanese (8) 8
German (6) 6
Spanish (6) 6
Chinese (4) 4
Polish (4) 4
French (3) 3
Czech (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neurology, ISSN 0028-3878, 10/2018, Volume 91, Issue 14, pp. e1368 - e1369
Journal Article
02/2014
Background: Alexander disease (AD) is a sporadic leukodystrophy that predominantly affects infants and children and usually results in death within ten years... 
Alexander Disease | Megalencephaly | Leukoencephalopathy | Alexander's leukodystrophy | Macrocephaly
Web Resource
Cell Stem Cell, ISSN 1934-5909, 11/2018, Volume 23, Issue 5, pp. 630 - 631
Gain-of-function mutations in the canonical astrocyte protein, GFAP, cause a fatal neurodevelopmental disorder with myelination abnormalities, seizures, and... 
ALEXANDER-DISEASE | CENTRAL-NERVOUS-SYSTEM | MUTATIONS | FIBRILLARY ACIDIC PROTEIN | CELL & TISSUE ENGINEERING | CELL BIOLOGY
Journal Article
Neurology, ISSN 0028-3878, 04/2018, Volume 90, Issue 20, pp. 925 - 930
Journal Article
Cell stem cell, ISSN 1934-5909, 8/2018, Volume 23, Issue 2, pp. 239 - 251.e6
Alexander disease (AxD) is a leukodystrophy that primarily affects astrocytes and is caused by mutations in the astrocytic filament gene GFAP . While... 
iPSCs | oligodendrocyte progenitor cells | myelination | Alexander disease | CHI3L1 | oligodendrocytes | leukodystrophy | astrocytes
Journal Article
Clinical Neurology, ISSN 0009-918X, 2018, Volume 58, Issue 3, pp. 198 - 201
Journal Article
Neurologia, ISSN 0213-4853, 2017
Introduction: Alexander disease is a rare disorder caused by mutations in the gene coding for glial fibrillary acidic protein (GFAP). In a previous study,... 
Glioma | NG2 | Alexander disease | Caspase-3 | GFAP
Journal Article
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, ISSN 0022-3050, 12/2017, Volume 88, Issue 12, pp. A61 - A61
Conference Proceeding
Neuropediatrics, ISSN 0174-304X, 2013, Volume 44, Issue 3, pp. 174 - 176
Journal Article
Pediatric Neurology, ISSN 0887-8994, 04/2019, Volume 93, pp. 61 - 62
Journal Article
JAMA Neurology, ISSN 2168-6149, 07/2017, Volume 74, Issue 7, pp. 869 - 869
Journal Article
Brain and Development, ISSN 0387-7604, 02/2019, Volume 41, Issue 2, pp. 195 - 200
Alexander disease (AxD) is a neurodegenerative disease in astrocytes caused by a mutation in the gene encoding glial fibrillary acidic protein, . We herein... 
Aggregation | Glial fibrillary acidic protein (GFAP) | Alexander disease (AxD) | Precocious puberty | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 2009, Volume 72, Issue 8, pp. 750 - 759
Journal Article
Histology and histopathology, ISSN 0213-3911, 04/2019, Volume 34, Issue 9, pp. 18110 - 1088
The various forms of Alexander disease (AD) have been linked to heterozygous point mutations in the coding region of the HUMAN GLIAL FIBRILLARY ACIDIC PROTEIN... 
Immunohistochemistry | Pathology | DIAGNOSIS | MRI | FIBRILLARY ACIDIC PROTEIN | Alexander disease | D128N GFAP mutation | MICE | ROSENTHAL FIBERS | CELL BIOLOGY
Journal Article
Brain and Development, ISSN 0387-7604, 04/2018, Volume 40, Issue 4, pp. 330 - 333
Infantile Alexander disease is a rare progressive leukodystrophy caused by autosomal dominant mutations in the (GFAP) gene typically presenting with... 
Alexander disease | Spinal manifestation | Leukodystrophy | GFAP | FIBRILLARY ACIDIC PROTEIN | ALEXANDER-DISEASE | CLINICAL NEUROLOGY | Index Medicus
Journal Article
Multiple Sclerosis and Related Disorders, ISSN 2211-0348, 2013, Volume 3, Issue 3, pp. 402 - 407
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.