The role of glial fibrillary acidic protein (GFAP) mutations in Alexander disease was analyzed in 44 patients, including 18 with later onset, at the University of Alabama, Birmingham, AL, and at other centers in the US, UK and Europe
Alexaneder disease (AxD) is a primary genetic disorder of astrocyte caused by mutations in the type ...
Researchers at the All India Institute of Medical Sciences, New Delhi, India, and VU University Medi...
To delineate the phenotype and genotype in Chinese children with type I Alexander disease (AxD) and ...
Alexander disease is a rare disorder of the central nervous system of unknown etiology. Infants with...
Alexander disease (AD), a rare neurodegenerative disorder of the central nervous system, is characte...
Heterozygous, de novo mutations in the glial fibrillary acidic protein (GFAP) gene have recently bee...
Alexander disease is a progressive, usually fatal neurological disorder defined by the widespread an...
Alexander disease is a degenerative white matter disorder due to mutations in the glial fibrillary a...
Pathogenic, dominant, de novo missense mutations in the glial fibrillary acidic protein (GFAP) have ...
[[abstract]]Alexander disease is a fatal neurological illness characterized by white-matter degenera...
Alexander disease (AxD) is a usually fatal astrogliopathy primarily caused by mutations in the gene ...
To characterize Alexander disease (AxD) phenotypes and determine correlations with age at onset (AAO...
ObjectiveTo characterize Alexander disease (AxD) phenotypes and determine correlations with age at o...
none17The purpose of this study was to describe unusual variants of Alexander's disease. We studied ...
Objective To report the clinical phenotype and genetic characteristics of an Alexander's disease typ...
Alexaneder disease (AxD) is a primary genetic disorder of astrocyte caused by mutations in the type ...
Researchers at the All India Institute of Medical Sciences, New Delhi, India, and VU University Medi...
To delineate the phenotype and genotype in Chinese children with type I Alexander disease (AxD) and ...
Alexander disease is a rare disorder of the central nervous system of unknown etiology. Infants with...
Alexander disease (AD), a rare neurodegenerative disorder of the central nervous system, is characte...
Heterozygous, de novo mutations in the glial fibrillary acidic protein (GFAP) gene have recently bee...
Alexander disease is a progressive, usually fatal neurological disorder defined by the widespread an...
Alexander disease is a degenerative white matter disorder due to mutations in the glial fibrillary a...
Pathogenic, dominant, de novo missense mutations in the glial fibrillary acidic protein (GFAP) have ...
[[abstract]]Alexander disease is a fatal neurological illness characterized by white-matter degenera...
Alexander disease (AxD) is a usually fatal astrogliopathy primarily caused by mutations in the gene ...
To characterize Alexander disease (AxD) phenotypes and determine correlations with age at onset (AAO...
ObjectiveTo characterize Alexander disease (AxD) phenotypes and determine correlations with age at o...
none17The purpose of this study was to describe unusual variants of Alexander's disease. We studied ...
Objective To report the clinical phenotype and genetic characteristics of an Alexander's disease typ...
Alexaneder disease (AxD) is a primary genetic disorder of astrocyte caused by mutations in the type ...
Researchers at the All India Institute of Medical Sciences, New Delhi, India, and VU University Medi...
To delineate the phenotype and genotype in Chinese children with type I Alexander disease (AxD) and ...
DOI
Add to ORKG