Results 151 to 160 of about 9,876 (239)

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients [PDF]

, 2009
Saara Tikka, Kati Mykkänen, Marie‐Magdeleine Ruchoux, Robert Bergholm, Maija Junna, Minna Pöyhönen, Hannele Yki‐Järvinen, Anne Joutel, Matti Viitanen, Marc Baumann, Hannu Kalimo   +10 more
openalex   +1 more source

NON-MIGRAINE RELATED PAIN BEHAVIOURS IN A TRANSGENIC "MIGRAINE MOUSE" WITH CIRCADIAN DISRUPTION [PDF]

, 2017
Goadsby, Peter J, Holland, Philip R, Holton, Christopher, Lopes, Douglas M, McMahon, Stephen B, Ptacek, Louis J, Strother, Lauren C   +6 more
core   +1 more source

Effects of Gender on the Phenotype of CADASIL [PDF]

, 2011
Bence Gunda, Dominique Hervé, O Godin, Martina Bruno, Sonia Reyes, Nassira Alili, Christian Opherk, Éric Jouvent, Marco Düring, Marie‐Germaine Bousser, Martin Dichgans, Hugues Chabriat   +11 more
openalex   +1 more source

First intravenous thrombolysis for pCys194Arg Notch 3 mutation in a Moroccan CADASIL patient with stroke

Radiology Case Reports
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene. Clinical manifestations of CADASIL include lacunar infarcts, transient ischemic attacks, dementia, migraine ...
Mohamed Amine Mnaili, MD
doaj  

The relation between cerebral small vessel function and white matter microstructure in monogenic and sporadic small vessel disease - the ZOOM@SVDs study. [PDF]

Cereb Circ Cogn Behav
Vlegels N, van den Brink H, Kopczak A, Arts T, Pham SDT, Siero JCW, Gesierich B, De Luca A, Duering M, Zwanenburg JJM, Dichgans M, Biessels GJ.   +11 more
europepmc   +1 more source

Is inadequate family history a barrier to diagnosis in CADASIL?

, 2005
Saif Razvi, R. Davidson, I Bone, Keith W. Muir   +3 more
openalex   +1 more source

Rapid improvement of a complex migrainous episode with sodium valproate in a patient with CADASIL [PDF]

, 2011
Mika H. Martikainen, Susanna Roine
openalex   +1 more source

NOTCH3 Variant Position Affects the Phenotype at the Pluripotent Stem Cell Level in CADASIL. [PDF]

Neuromolecular Med
Bugallo-Casal A, Muiño E, Bravo SB, Hervella P, Arias-Rivas S, Rodríguez-Yáñez M, Vara-León E, Quintas-Rey R, Pérez-Gayol L, Maisterra-Santos O, Pizarro-Gonzálvez J, Martorell-Riera MR, Vives-Bauzá C, Fernández-Cadenas I, Castillo J, Campos F.   +15 more
europepmc   +1 more source

Spontaneous lobar haemorrhage in CADASIL

, 2005
Ainsley Maclean
openalex   +1 more source

CADASIL Syndrome Presenting as Obsessive-Compulsive Disorder: A Case Report. [PDF]

Noro Psikiyatr Ars
Canlı D, Keskin M.
europepmc   +1 more source