Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Çağla Turan"'
Publikováno v:
Türk Patoloji Dergisi, Vol 37, Iss 3, Pp 264-265 (2021)
Lafora disease is a severe form of progressive myoclonic epilepsy with autosomal recessive inheritance diagnosed by inclusion body in biopsy. A 26-year-old woman was admitted due to complaints of frequent twitches and fainting. The 0.5x0.3x0.3 cm axi
Externí odkaz:
https://doaj.org/article/2f3a1e1373ed4c64bc07f7a6453ce915
Publikováno v:
Türk Patoloji Dergisi, Vol 37, Iss 3, Pp 264-265 (2021)
Lafora disease is a severe form of progressive myoclonic epilepsy with autosomal recessive inheritance diagnosed by inclusion body in biopsy. A 26-year-old woman was admitted due to complaints of frequent twitches and fainting. The 0.5x0.3x0.3 cm axi
Publikováno v:
Turkiye Klinikleri Journal of Neurology. 13:67-72
Publikováno v:
Turkiye Klinikleri Journal of Neurology. 13:84-88
Autor:
Mikail Bat, Çağla Turan Yurtseven
Publikováno v:
Gümüşhane Üniversitesi İletişim Fakültesi Elektronik Dergisi. 2
Social media that is appeared through new communication technologies attracts corporations’ attention because it is such a platform that individuals are connecting more each passing day. In the increasing competition environment, being in target gr