Zobrazeno 1 - 10
of 294
pro vyhledávání: '"KUMANDAŞ, Sefer"'
Autor:
Kanmaz, Seda, Kayilioglu, Hulya, Atas, Yavuz, Olculu, Cemile Busra, Dogan, Dilara Ece Toprak, Kart, Pinar Ozkan, Yildiz, Nihal, Gumus, Hakan, Per, Huseyin, Canpolat, Mehmet, Gulec, Ayten, Yildirim, Nalan, Turk, Emre, Celik, Neslihan, Ozturk, Selcan, Kumandas, Sefer, Kilic, Betul, Topcu, Yasemin, Ozpinar, Esra, Coskun, Aysenur, Arslan, Mutluay, Akkoyunlu, Deniz Sunnetci, Cine, Naci, Uzan, Gamze Sarikaya, Gunay, Cagatay, Akyol, Duygu, Ersoy, Ozlem, Direk, Meltem Cobanogullari, Komur, Mustafa, Kirkgoz, Hilal, Karaoğlu, Pakize, Ibis, Ipek Burcu Parlak, Cerci, Cisil, Orak, Ali, Oktay, Secil, Ayanoglu, Muge, Yildirim, Mirac, Bektas, Omer, Serdaroglu, Esra, Yilmaz, Sema Bozkaya, Cankurt, Ilknur, Hirfanoglu, Tugba, Arhan, Ebru, Gencpinar, Pinar, Dundar, Nihal Olgac, Teber, Serap, Serin, Hepsen Mine, Yilmaz, Sanem, Tosun, Ayse, Polat, Muzaffer, Yilmaz, Unsal, Unalp, Aycan, Kara, Bulent, Okuyaz, Cetin, Yis, Uluc, Hiz, Semra, Aktan, Gul, Gokben, Sarenur, Unay, Bulent, Serdaroglu, Ayse, Cansu, Ali, Aydin, Kursad, Tekgul, Hasan
Publikováno v:
In Seizure: European Journal of Epilepsy December 2024 123:17-25
Autor:
Acer, Hamit, Özçora, Gül Demet, Canpolat, Mehmet, Doğan, Muhammet Ensar, Karaman, Zehra Filiz, Kumandaş, Sefer
Publikováno v:
Journal of Pediatric Academy (J. Pediatr. Acad.); 2024, Vol. 5 Issue 3, p93-98, 6p
Publikováno v:
In Seizure: European Journal of Epilepsy February 2018 55:36-47
Autor:
Bayram, Ayşe Kaçar, Canpolat, Mehmet, Karacabey, Neslihan, Gumus, Hakan, Kumandas, Sefer, Doğanay, Selim, Arslan, Duran, Per, Hüseyin
Publikováno v:
In Brain and Development March 2016 38(3):274-279
Autor:
Bayram, Ayşe Kaçar ∗, Canpolat, Mehmet ∗, Çınar, Salih Levent †, Tahan, Fulya ‡, Gumus, Hakan ∗, Kumandaş, Sefer ∗, Per, Hüseyin ∗
Publikováno v:
In Journal of Emergency Medicine February 2016 50(2):e61-e66
Autor:
Canpolat, Mehmet, Kumandas, Sefer, Poyrazoglu, Hatice Gamze, Gumus, Hakan, Elmali, Ferhan, Per, Huseyin
Publikováno v:
In Seizure: European Journal of Epilepsy October 2014 23(9):708-716
Autor:
Per, Hüseyin, Canpolat, Mehmet, Gümüş, Hakan, Poyrazoğlu, Hatice Gamze, Yıkılmaz, Ali, Karaküçük, Sarper, Doğan, Hakkı, Kumandaş, Sefer
Publikováno v:
In Brain and Development June 2013 35(6):561-568
Autor:
Kiraz, Aslıhan, Gümüş, Hakan, Balta, Burhan, Erdoğan, Murat, Güven, Ahmet Sami, Savranlar, Ahmet, Çelik, Serkan Fazlı, Kumandaş, Sefer, Karaman, Zehra Filiz, Özdemir, Sevda Yeşim, Gümüş, Ümmü Gülsüm Özgül, Bayram, Nurettin, Per, Hüseyin
Publikováno v:
Journal of Clinical Practice & Research; Mar2023, Vol. 45 Issue 2, p152-158, 7p
Autor:
Kiraz, Aslıhan, Gümüş, Hakan, Balta, Burhan, Erdoğan, Murat, Güven, Ahmet Sami, Savranlar, Ahmet, Çelik, Serkan Fazlı, Kumandaş, Sefer, Karaman, Zehra Filiz, Özdemir, Sevda Yeşim, Özgül Gümüş, Ümmü Gülsüm, Bayram, Nurettin, Per, Hüseyin
Publikováno v:
Erciyes Medical Journal.
Makale
WOS:000925992500001
Objective: Neurofibromatosis type 1 (NF1, #162200) is a common neurological disorder with de novo or inherited germline mutations of the Neurofibromin (NF1, *613113). The purpose of this study is to increase the l
WOS:000925992500001
Objective: Neurofibromatosis type 1 (NF1, #162200) is a common neurological disorder with de novo or inherited germline mutations of the Neurofibromin (NF1, *613113). The purpose of this study is to increase the l
Autor:
Kumandaş, Sefer, Dündar, Munis, Özkul, Yusuf, Atasay, Rumeysa, Demir, Mikail, Erdoğan, Murat, Yıldırım, Abdulbaki, Gündüz, Cengiz
The Emanuel syndrome is a chromosomal disorder characterized by partial duplication of chromosomes 11 and 22, or supernumerary der(22)t(11;22). It is an unbalanced translocation syndrome, usually resulting from 3:1 meiosis I malsegregation during gam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9447::51b77cf24a076f69578982ed25081697
https://avesis.erciyes.edu.tr/publication/details/bedcca0f-ad41-4e28-90d3-e14ff930a156/oai
https://avesis.erciyes.edu.tr/publication/details/bedcca0f-ad41-4e28-90d3-e14ff930a156/oai