Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

By Tikka Saara  

Brain, Vol. 132, Iss. 4, 2009-04 ,pp. : 933-939

Oxford University Press

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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

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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

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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

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Cortical changes in cerebral small vessel diseases: a 3D MRI study of cortical morphology in CADASIL

By Jouvent Eric  

Brain, Vol. 131, Iss. 8, 2008-08 ,pp. : 2201-2208

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