(Q34989471)

5 August 2017

1 reference

title

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: phenotypic and mutational spectrum (English)

1 reference

5 August 2017

1

Martin Dichgans

1 reference

5 August 2017

publication date

1 November 2002

1 reference

Journal of the Neurological Sciences

5 August 2017

published in

1 reference

5 August 2017

volume

203-204

1 reference

5 August 2017

page(s)

77-80

1 reference

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

5 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

The natural history of CADASIL: a pooled analysis of previously published cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Phenotypic variability of CADASIL and novel morphologic findings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Quantitative MRI in CADASIL: correlation with disability and cognitive performance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Clinical severity in CADASIL related to ultrastructural damage in white matter: in vivo study with diffusion tensor MRI.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Schizophrenia in a patient with cerebral autosomally dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL disease)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Reversible coma with raised intracranial pressure: an unusual clinical manifestation of CADASIL

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Cerebrospinal fluid findings in CADASIL

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Binswanger's disease--revisited

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

The ins and outs of notch signaling

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Notch signaling: cell fate control and signal integration in development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Cerebral hemodynamics in CADASIL before and after acetazolamide challenge assessed with MRI bolus tracking

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Reduced cerebrovascular CO(2) reactivity in CADASIL: A transcranial Doppler sonography study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Prolonged cerebral transit time in CADASIL: a transcranial ultrasound study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Reduced vasomotor reactivity in cerebral microangiopathy : a study with near-infrared spectroscopy and transcranial Doppler sonography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Impaired cerebrovascular reactivity as a risk marker for first-ever lacunar infarction: A case-control study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Acetazolamide for the treatment of migraine with aura in CADASIL.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Cerebral microbleeds in CADASIL: a gradient-echo magnetic resonance imaging and autopsy study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Diagnostic Notch3 sequence analysis in CADASIL: three new mutations in Dutch patients. Dutch CADASIL Research Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Cerebral microbleeds in CADASIL.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2802%2900270-8

10.1016/S0022-510X(02)00270-8

7 January 2021

Identifiers

DOI

1 reference

5 August 2017

1 reference