Researchers at the All India Institute of Medical Sciences, New Delhi, India, and VU University Medical Center, Amsterdam report a 6-year-old Indian boy with infantile-onset Alexander disease having an unusually mild clinical course and a de novo mutation in the glial fibrillary acidic protein (GFAP) gene
Objectives: Alexander disease (AxD) is a rare autosomal dominant disorder due to GFAP mutations; inf...
Alexander disease (AD) is a leukodystrophy caused by heterozygous mutations in the gene encoding the...
The value of clinical and MRI criteria in the diagnosis of Alexander disease was determined by using...
Alexander disease is a degenerative white matter disorder due to mutations in the glial fibrillary a...
Background: Alexander disease (AD) is a sporadic leukodystrophy that predominantly affects infants a...
Alexander disease is an autosomal dominant leukoencephalopathy characterized by developmental delay,...
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 caused by mutations in the gene f...
Heterozygous, de novo mutations in the glial fibrillary acidic protein (GFAP) gene have recently bee...
The role of glial fibrillary acidic protein (GFAP) mutations in Alexander disease was analyzed in 44...
Alexander disease is a progressive, usually fatal neurological disorder defined by the widespread an...
Alexander’s disease is a rare, generally sporadic, fatal dis-order of the central nervous system. It...
Alexander Disease (ALXDRD) is an autosomal dominant leukodystrophy caused by mutation in one allele ...
Alexander disease is a rare disorder of the central nervous system of unknown etiology. Infants with...
To delineate the phenotype and genotype characteristics in 12 Chinese children with Alexander diseas...
Objectives: Alexander disease (AxD) is a rare autosomal dominant disorder due to GFAP mutations; inf...
Alexander disease (AD) is a leukodystrophy caused by heterozygous mutations in the gene encoding the...
The value of clinical and MRI criteria in the diagnosis of Alexander disease was determined by using...
Alexander disease is a degenerative white matter disorder due to mutations in the glial fibrillary a...
Background: Alexander disease (AD) is a sporadic leukodystrophy that predominantly affects infants a...
Alexander disease is an autosomal dominant leukoencephalopathy characterized by developmental delay,...
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 caused by mutations in the gene f...
Heterozygous, de novo mutations in the glial fibrillary acidic protein (GFAP) gene have recently bee...
The role of glial fibrillary acidic protein (GFAP) mutations in Alexander disease was analyzed in 44...
Alexander disease is a progressive, usually fatal neurological disorder defined by the widespread an...
Alexander’s disease is a rare, generally sporadic, fatal dis-order of the central nervous system. It...
Alexander Disease (ALXDRD) is an autosomal dominant leukodystrophy caused by mutation in one allele ...
Alexander disease is a rare disorder of the central nervous system of unknown etiology. Infants with...
To delineate the phenotype and genotype characteristics in 12 Chinese children with Alexander diseas...
Objectives: Alexander disease (AxD) is a rare autosomal dominant disorder due to GFAP mutations; inf...
Alexander disease (AD) is a leukodystrophy caused by heterozygous mutations in the gene encoding the...
The value of clinical and MRI criteria in the diagnosis of Alexander disease was determined by using...
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