Results 111 to 120 of about 9,876 (239)
Screening British CADASIL families for mutations in the NOTCH3 gene [PDF]
, 2000 R.P.J. de Lange
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Description of a simple test for CADASIL disease and determination of mutation frequencies in sporadic ischaemic stroke and dementia patients [PDF]
, 2000 Tengyao Wang
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CADASIL AND BIPOLAR AFFECTIVE DISORDER [PDF]
, 2019 Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a rare monogenic disorder caused by mutations in the NOTCH3 gene.
A. Millar, Zachary +2 more
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Phenotype of a Homozygous CADASIL Patient in Comparison to 9 Age-Matched Heterozygous Patients With the Same R133C Notch3 Mutation [PDF]
, 2001 Susanna Tuominen +11 more
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Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy – CADASIL
Clinical and Biomedical Research, 2017 We report here neuroimaging findings of a 41 years-old female with molecular diagnosis of CADASIL (Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy).
Rosane Brondani +8 more
doaj
An Animal Model for the Molecular Genetics of CADASIL [PDF]
, 2001 Karl J. Fryxell +2 more
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The pathomechanism and treatment of CADASIL
Rinsho Shinkeigaku, 2011 CADASIL has been reported notably in Europe, has recently been found to occur in Japan and, with the increase in the number of reported cases, has been attracting attention. Currently, the diagnosis of CADASIL is established clinically if the patient: (1) develops the condition at a relatively young age (40-50 years), (2) is not at risk for stroke, (3)
openaire +4 more sources
A Diagnostic view of the Genetics of CASADIL [PDF]
, 2009 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL, OMIM #125310) is an inherited vascular disease. The main symptoms include migraineous headache, recurrent strokes and progressive cognitive impairment ...
Mykkänen, Kati
core
False-Negative Tests in CADASIL [PDF]
, 2001 Gabriel Ribeiro de Freitas +4 more
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