A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation.
about
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation.Palatal tremor, progressive multiple cranial nerve palsies, and cerebellar ataxia: a case report and review of literature of palatal tremors in neurodegenerative disease.Alexander's disease: clinical, pathologic, and genetic features.Autonomic dysfunction in adult-onset alexander disease: a case report and review of the literature.Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortex.Encephalopathies with intracranial calcification in children: clinical and genetic characterization
P2860
A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
A familial disorder associated ...... and Rosenthal fibre formation.
@en
type
label
A familial disorder associated ...... and Rosenthal fibre formation.
@en
prefLabel
A familial disorder associated ...... and Rosenthal fibre formation.
@en
P2093
P2860
P356
P1476
A familial disorder associated ...... and Rosenthal fibre formation.
@en
P2093
Greenwood R
Harding AE
Scaravilli F
P2860
P304
P356
10.1136/JNNP.56.9.977
P407
P577
1993-09-01T00:00:00Z