A patient with Parkinson’s disease carrying a rare variant in the kinase domain of LRRK2

by Halil Onder, Vehap Topcu, Selcuk Comoglu
Published 2023-01-01

A juvenile-onset case of autosomal recessive spastic ataxia of charlevoix–saguenay with a novel mutation in the SACS gene

by Halil Onder, Vehap Topcu, Selcuk Comoglu
Published 2023-01-01

EFFECT OF HEREDITARY THROMBOPHILIA ON ARTERIAL THROMBOSIS

by Ferda Can, Tansu Büyükgül, Nuray Yılmaz Cakmak, Ihsan Ates, Vehap Topcu, Said Furkan Yıldırım, Sema Akıncı
Published 2024-05-01