Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
about
Microvascular pathology and morphometrics of sporadic and hereditary small vessel diseases of the brainCADASIL: hereditary disease of arteries causing brain infarcts and dementia.CADASIL: hereditary arteriopathy leading to multiple brain infarcts and dementia.Accuracy of clinical diagnosis in primary degenerative dementia: correlation with neuropathological findingsHereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneityNew phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical featureCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease.Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families.Notch deficiency implicated in the pathogenesis of congenital disorder of glycosylation IIcCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family.Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.Genetics of ischaemic stroke; single gene disorders.Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variantReview: molecular genetics and pathology of hereditary small vessel diseases of the brain.Changing clinical patterns and increasing prevalence in CADASIL.CADASIL: Treatment and Management Options.Atypical dementia syndrome in an elderly man.Heterogeneity of vascular dementia: mechanisms and subgroups.Recent advances in the genetics of Alzheimer's disease and vascular dementia with an emphasis on gene-environment interactions.Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease.Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases.Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1.CADASIL syndrome: a genetic form of vascular dementia.Vascular dementia: a contemporary review of epidemiology, diagnosis, prevention, and treatment.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Neuropathological and in vitro studies of abnormal elastogenesis.Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathy.CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): a neurovascular disease diagnosed by ultrastructural examination of the skin.Update on Vascular Cognitive Impairment Associated with Subcortical Small-Vessel Disease.The C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene and vascular dementia.Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
P2860
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P2860
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年学术文章
@wuu
1977年学术文章
@zh
1977年学术文章
@zh-cn
1977年学术文章
@zh-hans
1977年学术文章
@zh-my
1977年学术文章
@zh-sg
1977年學術文章
@yue
1977年學術文章
@zh-hant
name
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
@en
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
@nl
type
label
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
@en
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
@nl
prefLabel
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
@en
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
@nl
P356
P1476
Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.
@en
P2093
J Wålinder
P Sourander
P2888
P304
P356
10.1007/BF00691704
P577
1977-08-01T00:00:00Z