Cerebral calcifications and cerebellar hypoplasia in two children: clinical, radiologic and neuropathological studies--a separate neurodevelopmental entity.
about
The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).Aicardi-Goutières syndrome: clinical and neuroradiological findings of 10 new cases.Recurrent pseudo-TORCH appearances of the brain presenting as "Dandy-Walker" malformation.
P2860
Cerebral calcifications and cerebellar hypoplasia in two children: clinical, radiologic and neuropathological studies--a separate neurodevelopmental entity.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年学术文章
@wuu
1984年学术文章
@zh
1984年学术文章
@zh-cn
1984年学术文章
@zh-hans
1984年学术文章
@zh-my
1984年学术文章
@zh-sg
1984年學術文章
@yue
1984年學術文章
@zh-hant
name
Cerebral calcifications and ce ...... ate neurodevelopmental entity.
@en
Cerebral calcifications and ce ...... ate neurodevelopmental entity.
@nl
type
label
Cerebral calcifications and ce ...... ate neurodevelopmental entity.
@en
Cerebral calcifications and ce ...... ate neurodevelopmental entity.
@nl
prefLabel
Cerebral calcifications and ce ...... ate neurodevelopmental entity.
@en
Cerebral calcifications and ce ...... ate neurodevelopmental entity.
@nl
P2093
P356
P1433
P1476
Cerebral calcifications and ce ...... ate neurodevelopmental entity.
@en
P2093
Veiga Pires J
Willemse J
van Rossum A
P304
P356
10.1055/S-2008-1052350
P577
1984-05-01T00:00:00Z