Results 131 to 140 of about 3,805 (159)

CYSTEINE-SPARING NOTCH3 MUTATIONS: CADASIL OR CADASIL VARIANTS?

Neurology, 2008
Copyright (2008) LIPPINCOTT WILLIAMS ...
Scheid, R., Heinritz, W., Leyhe, T., Thal, D., Schober, R., Strenge, S., von Cramon, D., Froster, U.   +7 more
openaire   +4 more sources

The pathogenesis of CADASIL: an update

Journal of the Neurological Sciences, 2004
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) appears to be the most common form of hereditary stroke disorder. CADASIL is associated with arterial smooth muscle degeneration linked to mutations in the Notch3 gene, whose product is a transmembrane receptor that functions in cell-cell communication.
R N, Kalaria, M, Viitanen, H, Kalimo, M, Dichgans, T, Tabira   +4 more
openaire   +2 more sources

CADASIL

Advances in Anatomic Pathology, 1998
M. Dichgans, T. Gasser
  +5 more sources

Active immunotherapy reduces NOTCH3 deposition in brain capillaries in a CADASIL mouse model

EMBO Molecular Medicine, 2023
Daniel V Oliveira, Kirsten G Coupland, Shaobo Jin   +2 more
exaly  

Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations

CNS Neuroscience and Therapeutics, 2022
Wang Ni, Juan-Juan Xie, Hong-Fu Li
exaly  

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

Lancet, The, 1997
Anne Joutel, K Vahedi, Christophe Corpechot   +2 more
exaly  

CADASIL ☆

2003
openaire   +1 more source

Interpretation ofNOTCH3mutations in the diagnosis of CADASIL

Expert Review of Molecular Diagnostics, 2014
Julie W Rütten, J Haan, Gisela M Terwindt   +2 more
exaly  

CADASIL Notch3 Mutant Proteins Localize to the Cell Surface and Bind Ligand

Circulation Research, 2002
Talin Haritunians, Carol Hicks, Gerry Weinmaster   +2 more
exaly  

The Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale

Stroke, 2012
Francesca Pescini, Serena Nannucci, Bruno Bertaccini   +2 more
exaly