Literature DB >> 22955859

First report of a Tunisian CADASIL patient.

Michele Ragno, Katia Nardi, Antonio Manca, Manrico Morroni, Luigi Trojano.   

Abstract

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Year:  2012        PMID： 22955859     DOI： 10.1007/s10072-012-1184-9

Source DB:  PubMed          Journal:  Neurol Sci        ISSN： 1590-1874            Impact factor:   3.307


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  8 in total

1.  p.Arg332Cys mutation of NOTCH3 gene in two unrelated Japanese families with CADASIL.

Authors:  Yasuteru Sano; Fumitaka Shimizu; Motoharu Kawai; Masatoshi Omoto; Kiyoshi Negoro; Tetsu Kurokawa; Hirosuke Fujisawa; Michiyasu Suzuki; Naoko Okayama; Yutaka Suehiro; Yuji Hinoda; Takashi Kanda
Journal:  Intern Med       Date:  2011-11-15       Impact factor: 1.271

Review 2.  The spectrum of mutations for CADASIL diagnosis.

Authors:  A Federico; S Bianchi; M T Dotti
Journal:  Neurol Sci       Date:  2005-06       Impact factor: 3.307

3.  A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings.

Authors:  R L Oliveri; M Muglia; N De Stefano; R Mazzei; A Labate; F L Conforti; A Patitucci; A L Gabriele; G Tagarelli; A Magariello; M Zappia; A Gambardella; A Federico; A Quattrone
Journal:  Arch Neurol       Date:  2001-09

4.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy affecting an African American man: identification of a novel 15-base pair NOTCH3 duplication.

Authors:  Soo Jung Lee; He Meng; Omar Elmadhoun; Mila Blaivas; Michael Mei-Hwa Wang
Journal:  Arch Neurol       Date:  2011-12

5.  Subcortical lacunar lesions: an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  Rivka van Den Boom; Saskia A J Lesnik Oberstein; Sjoerd G van Duinen; Marjolijn Bornebroek; Michel D Ferrari; Joost Haan; Mark A van Buchem
Journal:  Radiology       Date:  2002-09       Impact factor: 11.105

6.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Authors:  Chris Retief; Clara-Maria Schutte; Malcolm Kevin Baker
Journal:  S Afr Med J       Date:  2009-06

7.  Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation.

Authors:  M Ragno; G Cacchiò; G M Fabrizi; M Scarcella; F Silvaggio; T Cavallaro; F Taioli; L Trojano
Journal:  Neurol Sci       Date:  2007-08-10       Impact factor: 3.307

8.  The phenotypic spectrum of CADASIL: clinical findings in 102 cases.

Authors:  M Dichgans; M Mayer; I Uttner; R Brüning; J Müller-Höcker; G Rungger; M Ebke; T Klockgether; T Gasser
Journal:  Ann Neurol       Date:  1998-11       Impact factor: 10.422
  8 in total
  2 in total

Review 1.  Neurogenomics in Africa: Perspectives, progress, possibilities and priorities.

Authors:  Rufus O Akinyemi; Mayowa O Owolabi; Tolulope Oyeniyi; Bruce Ovbiagele; Donna K Arnett; Hemant K Tiwari; Richard Walker; Adesola Ogunniyi; Raj N Kalaria
Journal:  J Neurol Sci       Date:  2016-05-06       Impact factor: 3.181

2.  CADASIL: Ultrastructural insights into the morphology of granular osmiophilic material.

Authors:  Teresa Lorenzi; Michele Ragno; Francesca Paolinelli; Clara Castellucci; Marina Scarpelli; Manrico Morroni
Journal:  Brain Behav       Date:  2017-02-22       Impact factor: 2.708
  2 in total

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