Results 81 to 90 of about 14,274 (181)
Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL
Folia Neuropathologica, 2020 Jolanta Dorszewska +8 more
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Prominent juxtacortical white matter lesion hallmarks NOTCH3-related intracerebral haemorrhage
Stroke and Vascular NeurologyBackground and purpose NOTCH3 p.R544C mutation accounts for 5% of spontaneous intracerebral haemorrhage (ICH) in East Asian patients. We investigated whether certain CT features are associated with NOTCH3-related ICH.Methods Patients with spontaneous ICH
Sung-Chun Tang +5 more
doaj +1 more source
Top-NOTCH3 Variants in the Population at Large [PDF]
Stroke, 2020 Raj N. Kalaria, Steven J. Kittner
openaire +2 more sources
Scientific ReportsNOTCH receptor 3 (NOTCH3) is known to regulate the transcription of oncogenes or tumor suppressor genes, thereby playing a crucial role in tumor development, invasion, maintenance, and chemotherapy resistance.
Jia Xu +7 more
doaj +1 more source
NOTCH3-related CADASIL and Non-NOTCH3-related CADASIL-like syndrome
Nosotchu, 2008 Mizuno, Toshiki +5 more
openaire +2 more sources
Association of imaging-defined brain age with disease severity and adverse outcomes in CADASIL. [PDF]
Alzheimers DementHsu SL +7 more
europepmc +1 more source
A novel missense variant Cys559Gly in <i>NOTCH3</i> in CADASIL family and vascular lesions in patients with migraine. [PDF]
Postep Psychiatr NeurolJastrzębski K +4 more
europepmc +1 more source
Inflammatory CADASIL: the cross-link between CADASIL and multiple sclerosis: a report of two cases and systematic review of the literature. [PDF]
BMC NeurolAhmed AM, Mistry N, Gehad AS, Hassan AM.
europepmc +1 more source