Yazar "Kısabay, Ayşın" için listeleme
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Cadasil with atypical clinical symptoms, magnetic resonance imaging, and novel mutations: Two case reports and a review of the literature
Sarı, Ümmü Serpil; Kısabay, Ayşın; Batum, Melike; Tarhan, Serdar; Doğan, Nihal; Coşkunoğlu, Aysun; Cam, Sırrı; Yılmaz, Hikmet; Selçuki, Deniz (Humana Press INC, 2019)Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary microangiopathy with adult onset caused by a missense mutation in the NOTCH3 gene in chromosome 19p13. ...
