Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases. (Q44494580)

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23 February 2020

title

Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases (English)

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23 February 2020

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1

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23 February 2020

Yumi Yamamoto

12

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23 February 2020

Catriona A. McLean

8

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23 February 2020

Vincent Deramecourt

13

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23 February 2020

author name string

Christian Hagel

2

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23 February 2020

Gregor Kuhlenbaeumer

3

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23 February 2020

Anne Borjesson-Hanson

4

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23 February 2020

Oluf Andersen

5

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23 February 2020

Matti Viitanen

6

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23 February 2020

Hannu Kalimo

7

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23 February 2020

Janet Y Slade

9

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23 February 2020

Roslyn A Hall

10

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23 February 2020

Arthur E Oakley

11

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23 February 2020

Rajesh N Kalaria

14

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23 February 2020

language of work or name

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8 March 2013

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23 February 2020

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23 February 2020

volume

23

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23 February 2020

issue

5

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23 February 2020

page(s)

547-557

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Novel ophthalmological features in hereditary endotheliopathy with retinopathy, nephropathy and stroke syndrome

23 February 2020

cites work

1 reference

Staging and natural history of cerebrovascular pathology in dementia

21 January 2018

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MRI features of pontine autosomal dominant microangiopathy and leukoencephalopathy (PADMAL).

21 January 2018

1 reference

The arterial lesions underlying lacunes

21 January 2018

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Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL.

21 January 2018

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Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).

21 January 2018

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Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature

21 January 2018

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Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

21 January 2018

1 reference

Towards defining the neuropathological substrates of vascular dementia.

21 January 2018

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The pathogenesis of CADASIL: an update

21 January 2018

1 reference

Nonhypertensive cerebral small-vessel disease. An autopsy study.

21 January 2018

1 reference

Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL.

21 January 2018

1 reference

Arterioles of the lenticular nucleus in CADASIL.

21 January 2018

1 reference

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3

21 January 2018

1 reference

C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

21 January 2018

1 reference

Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.

21 January 2018

1 reference

Risk factors for silent cerebral infarcts in subcortical white matter and basal ganglia.

21 January 2018

1 reference

Review: molecular genetics and pathology of hereditary small vessel diseases of the brain.

21 January 2018

1 reference

Neuropathological correlates of temporal pole white matter hyperintensities in CADASIL.

21 January 2018

1 reference

The microvascular changes in cases of hereditary multi-infarct disease of the brain

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/BPA.12041

1 reference

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23 February 2020

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