Cite
Moyamoya Syndrome as a rare vasculopathy of the Central Nervous System in children with Neurofibromatosis Type 1
MLA
Delin, Sanja, et al. Moyamoya Syndrome as a Rare Vasculopathy of the Central Nervous System in Children with Neurofibromatosis Type 1. Jan. 2019. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.57a035e5b1ae..447508e7ffd0593733c11d1d2fc91dbe&authtype=sso&custid=ns315887.
APA
Delin, S., Kovač Šižgorić, M., Krakar, G., Đuranović, V., & Sabol, Z. (2019). Moyamoya Syndrome as a rare vasculopathy of the Central Nervous System in children with Neurofibromatosis Type 1.
Chicago
Delin, Sanja, Matilda Kovač Šižgorić, Goran Krakar, Vlasta Đuranović, and Zlatko Sabol. 2019. “Moyamoya Syndrome as a Rare Vasculopathy of the Central Nervous System in Children with Neurofibromatosis Type 1,” January. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.57a035e5b1ae..447508e7ffd0593733c11d1d2fc91dbe&authtype=sso&custid=ns315887.