CADASIL

Citations 21-26 of 26 total displayed.

Past content (since Mar 2001):

BRIEF COMMUNICATIONS
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL

A. Malandrini, F. Albani, S. Palmeri, F. Fattapposta, S. Gambelli, G. Berti, A. Bracco, A. Tammaro, S. Calzavara, M. Villanova, M. Ferrari, A. Rossi, and P. Carrera
Neurology 2002; 59: 617-620. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke

J. F. Arboleda–Velasquez, F. Lopera, E. Lopez, M. P. Frosch, D. Sepulveda–Falla, J. E. Gutierrez, S. Vargas, M. Medina, C. Martinez de Arrieta, R. V. Lebo, S. A. Slaugenhaupt, R. A. Betensky, A. Villegas, M. Arcos–Burgos, D. Rivera, J. C. Restrepo, and K. S. Kosik
Neurology 2002; 59: 277-279. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

Sohei Yanagawa, Nobuo Ito, Kunimasa Arima, and Shu-ichi Ikeda
Neurology 2002; 58: 817-820. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL

Martin Dichgans, Jürgen Herzog, and Thomas Gasser
Neurology 2001; 57: 1714-1717. [Abstract] [Full text] [PDF]  

ARTICLES
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family

P. de la Peña, B. Bornstein, P. del Hoyo, M. A. Fernández–Moreno, M. A. Martín, Y. Campos, C. Gómez–Escalonilla, J. A. Molina, A. Cabello, J. Arenas, and R. Garesse
Neurology 2001; 57: 1235-1238. [Abstract] [Full text] [PDF]  

ARTICLES
Altered white and gray matter metabolism in CADASIL: A proton MR spectroscopy and ¹H-MRSI study

D. P. Auer, T. Schirmer, J. O. Heidenreich, J. Herzog, B. Pütz, and M. Dichgans
Neurology 2001; 56: 635-642. [Abstract] [Full text] [PDF]  

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