http://www.cnr.it/ontology/cnr/individuo/prodotto/ID50265
A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL (Articolo in rivista)
- Type
- Label
- A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1007/s10072-009-0040-z (literal)
- Alternative label
Ungaro C, Servillo P, Mazzei R, Consoli D, Conforti FL, Sprovieri T, Lanza PL, Quattrone A. (2009)
A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL
in Neurological sciences (Testo stamp.)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Ungaro C, Servillo P, Mazzei R, Consoli D, Conforti FL, Sprovieri T, Lanza PL, Quattrone A. (literal)
- Pagina inizio
- Pagina fine
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- Rivista
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Institute of Neurological Sciences, National Research Council,
Loc. Burga, 87050 Piano Lago di Mangone (CS), Italy;
Department of Neurosciences, Psychiatric and Anesthesiological
Sciences, University of Messina, Messina, Italy;
Neurology Unit, ''G. Jazzolino'' Hospital, Vibo Valentia, Italy;
Institute of Neurology, University ''Magna Graecia'',
Catanzaro, Italy (literal)
- Titolo
- A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASIL (literal)
- Abstract
- Cerebral Autosomal Dominant Arteriopathy with Subcortical
Infarcts and Leukoencephalopathy (CADASIL, MIM
125310) is an inherited vascular dementia caused by
mutations in the NOTCH3 gene. The clinical phenotypic
spectrum of the disease is characterized by recurrent subcortical
ischemic strokes and white matter lesions in brain
magnetic resonance images (MRI); additional symptoms
such as progressive cognitive disorder, mood disturbance,
and migraine with aura are often observed, Here, we
report an Italian patient affected by CADASIL in whom a
rare missense mutation was detected on exon 22. The same
patient was included in a previous collaborative study in
which the Italian CADASIL mutations were summarized in
a review (literal)
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