Microgyria and cytomegalic inclusion disease in infancy.
about
Polymicrogyria: a common and heterogeneous malformation of cortical development.Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patientsX-linked malformations of cortical development.Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposisDevelopmental analysis of the cytomegalovirus enhancer in transgenic animals.Cytomegalic inclusion diseasePrevalence of cytomegalovirus in France.THE INCIDENCE OF INFECTION WITH CYTOMEGALOVIRUS IN A NORMAL POPULATION. A SEROLOGICAL STUDY IN GREATER LONDONRetinoic acid receptors initiate induction of the cytomegalovirus enhancer in embryonal cells.[Cytomegaly and central nervous system abnormalities. Report of 2 cases associated with agenesia of the corpus callosum and cystic encephalopathy]Ultra-high-field MR imaging in polymicrogyria and epilepsyHomozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria.Isolation of cytomegalovirus and clinical manifestations of infection at different ages.Malformations of cortical development and epilepsy
P2860
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P2860
Microgyria and cytomegalic inclusion disease in infancy.
description
1959 nî lūn-bûn
@nan
1959年の論文
@ja
1959年論文
@yue
1959年論文
@zh-hant
1959年論文
@zh-hk
1959年論文
@zh-mo
1959年論文
@zh-tw
1959年论文
@wuu
1959年论文
@zh
1959年论文
@zh-cn
name
Microgyria and cytomegalic inclusion disease in infancy.
@ast
Microgyria and cytomegalic inclusion disease in infancy.
@en
type
label
Microgyria and cytomegalic inclusion disease in infancy.
@ast
Microgyria and cytomegalic inclusion disease in infancy.
@en
prefLabel
Microgyria and cytomegalic inclusion disease in infancy.
@ast
Microgyria and cytomegalic inclusion disease in infancy.
@en
P2860
P356
P1476
Microgyria and cytomegalic inclusion disease in infancy.
@en
P2093
P2860
P304
P356
10.1136/JCP.12.5.427
P407
P577
1959-09-01T00:00:00Z