CADASIL: what component of the vessel wall is really a target for Notch 3 gene mutations?

By Rafalowska Janina   Dziewulska Dorota   Fidzianska Anna  

Neurological Research, Vol. 26, Iss. 5, 2004-07 ,pp. : 558-562

Maney Publishing

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Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain

By Monet-Leprêtre Marie  

Brain, Vol. 132, Iss. 6, 2009-06 ,pp. : 1601-1612

Oxford University Press

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“CADASIL coma” in an Italian homozygous CADASIL patient: comparison with clinical and MRI findings in age-matched heterozygous patients with the same G528C NOTCH3 mutation

By Ragno Michele   Pianese Luigi   Morroni Manrico   Cacchiò Gabriella   Manca Antonio   Marzio Fabio   Silvestri Serena   Miceli Cristina   Scarcella Maria   Onofrj Marco   Trojano Luigi  

Neurological Sciences, Vol. 34, Iss. 11, 2013-11 ,pp. : 1947-1953

Springer Publishing Company

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An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene

By Guidetti D.   Casali B.   Mazzei R.   Cenacchi G.   Berti G.   Zuccoli G.   Nicoli D.   Conforti F.   Sprovieri T.   Pasquinelli G.   Brini M.  

Neurological Sciences, Vol. 24, Iss. 6, 2004-02 ,pp. : 401-406

Springer Publishing Company

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Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene

By Ragno M.   Fabrizi G.   Cacchiò G.   Scarcella M.   Sirocchi G.   Selvaggio F.   Taioli F.   Ferrarini M.   Trojano L.  

Neurological Sciences, Vol. 27, Iss. 4, 2006-09 ,pp. : 252-256

Springer Publishing Company

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