Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome.
about
Cerebral small vessel disease: Capillary pathways to stroke and cognitive declineHereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3Genetics of vascular dementia - review from the ICVD working group.Neuroimaging of cerebral small vessel disease.[HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy]New roles for the major human 3'-5' exonuclease TREX1 in human disease.Retinal vascular image analysis as a potential screening tool for cerebrovascular disease: a rationale based on homology between cerebral and retinal microvasculatures.Hereditary endotheliopathy with retinopathy and encephalopathy: pathological and genetic studies of a familyMigraine and genetic and acquired vasculopathies.Migraine and neurogenetic disorders.Neuropathology and genetics of cerebroretinal vasculopathies.Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations.TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy.C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.A 44-year-old man with eye, kidney, and brain dysfunction.Multiple sclerosis-like lesions and type I interferon signature in a patient with RVCL.Hereditary systemic angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy, and hepatopathy.A gene for a new monogenic neurovascular migraine syndrome: a next step in unravelling molecular pathways for migraine?
P2860
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P2860
Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Cerebroretinal vasculopathy mi ...... of a rare hereditary syndrome.
@en
Cerebroretinal vasculopathy mi ...... of a rare hereditary syndrome.
@nl
type
label
Cerebroretinal vasculopathy mi ...... of a rare hereditary syndrome.
@en
Cerebroretinal vasculopathy mi ...... of a rare hereditary syndrome.
@nl
prefLabel
Cerebroretinal vasculopathy mi ...... of a rare hereditary syndrome.
@en
Cerebroretinal vasculopathy mi ...... of a rare hereditary syndrome.
@nl
P2093
P356
P1433
P1476
Cerebroretinal vasculopathy mi ...... of a rare hereditary syndrome.
@en
P2093
P304
P356
10.1212/WNL.53.3.629
P407
P577
1999-08-01T00:00:00Z