Sennur Delibaş

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CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a rare autosomal dominant genetic disease characterized with recurrent stroke, migrainous headache, cognitive deficits, and psychiatric symptoms associated with mutations in the NOTCH 3 gene on chromosome 19. Here, we report a case of CADASIL who(More)
Keeping in mind that lesions located in the splenium of the corpus callosum can sometimes be temporary may help us avoid invasive diagnostic and therapeutic methods. Transient lesion in the splenium of the corpus related to using or withdrawal of antiepileptic drugs are rarely encountered. In this article, we present a non-epileptic patient found to have a(More)
Factors related with hyperhomocysteinemia (HHcy) and the impact of HHcy in Parkinson's disease (PD) are not well understood. We investigated the factors associated with increased levels of homocysteine (Hcy) and the relationship between HHcy and motor symptoms, cognitive status, and vascular risk in patients with Parkinson's disease. Among 60 patients (29(More)
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