(Q34305487)

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Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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Europe PubMed Central

PubMed publication ID

1 August 2017

Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

M M Ruchoux

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

D Guerouaou

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

B Vandenhaute

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

J P Pruvo

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

P Vermersch

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

D Leys

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

1 January 1995

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Europe PubMed Central

PubMed publication ID

1 August 2017

Acta Neuropathologica

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Europe PubMed Central

PubMed publication ID

1 August 2017

89

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

500-512

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Europe PubMed Central

PubMed publication ID

1 August 2017

Juvenile arteriosclerotic leukoencephalopathy: anatomoclinical study of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cicletanine and hypertensive retinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Small arterial granular degeneration in familial Binswanger's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BINSWANGER'S PROGRESSIVE SUBCORTICAL VASCULAR ENCEPHALOPATHY. A CLINICO-NEUROPATHOLOGICAL STUDY

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein E polymorphism and atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The vascularization of the human cerebellar cortex

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features of subcortical arteriosclerotic encephalopathy (Binswanger disease)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endothelium-dependent contractions in arteries and veins

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms of structural vascular changes in genetic hypertension: analyses on cultured vascular smooth muscle cells from spontaneously hypertensive rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructural changes in cerebral pericytes and astrocytes of stroke-prone spontaneously hypertensive rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Effects of cicletanine on kidney lesions associated with age. Light and electron microscopy studies]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endothelin-1-like immunoreactivity is expressed in human reactive astrocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beta-amyloid formation by myocytes of leptomeningeal vessels

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations in vascular smooth muscle mass in the spontaneously hypertensive rat. Role of cellular hypertrophy, hyperploidy, and hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial unusual encephalopathy of Binswanger's type without hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arteriolar tortuosity of the white matter in aging and hypertension. A microradiographic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of cicletanine on cerebrovascular injury in stroke-prone spontaneously hypertensive rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protective action of cicletanine on the vascular walls in stroke-prone spontaneously hypertensive rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial disorder with subcortical ischemic strokes, dementia, and leukoencephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenesis of Binswanger chronic progressive subcortical encephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathological proteins Tau 64 and 69 are specifically expressed in the somatodendritic domain of the degenerating cortical neurons during Alzheimer's disease. Demonstration with a panel of antibodies against Tau proteins.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Astrocytes induce blood–brain barrier properties in endothelial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cortical blood vessels of the human brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial subcortical dementia with arteriopathic leukoencephalopathy. A clinico-pathological case

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary multi-infarct dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predictive and preventive pathology of cardiovascular diseases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic progressive leukoencephalopathy with systemic arteriosclerosis in young adults

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructural Study of the Choroid Plexus of Spontaneously Hypertensive Rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic familial vascular encephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21, 1993.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Binswanger's disease: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The arteriole as a site of metabolic exchange

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Arteriopathic leukoencephalopathy (17 anatomo-clinical cases)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

White matter lesions on magnetic resonance imaging in clinically diagnosed Alzheimer's disease. Evidence for heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/7676806

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S004010050281

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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