Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Yılmaz, Cahide"'
Autor:
Gurkas, Esra, Karalok, Zeynep S., Taskin, Birce D., Aydogmus, Ummu, Guven, Alev, Degerliyurt, Aydan, Bektas, Omer, Yilmaz, Cahide
Publikováno v:
In Brain and Development October 2016 38(9):827-834
Autor:
Davarci, Isil, Karcioglu, Murat, Tuzcu, Kasim, Basarslan, Fatmagul, Davran, Ramazan, Yengil, Erhan, Yilmaz, Cahide, Turhanoglu, Selim
Publikováno v:
In Brazilian Journal of Anesthesiology (Edicion en espanol) September-October 2014 64(5):320-325
Autor:
Davarci, Isil, Karcioglu, Murat, Tuzcu, Kasim, Basarslan, Fatmagul, Davran, Ramazan, Yengil, Erhan, Yilmaz, Cahide, Turhanoglu, Selim
Publikováno v:
In Brazilian Journal of Anesthesiology (English edition) September-October 2014 64(5):320-325
Autor:
Yuca, Sevil Ari, Rendtorff, Nanna Dahl, Boulahbel, Houda, Lodahl, Marianne, Tranebjærg, Lisbeth, Cesur, Yasar, Dogan, Murat, Yilmaz, Cahide, Akgun, Cihangir, Acikgoz, Mehmet
Publikováno v:
In European Journal of Medical Genetics January 2012 55(1):37-42
Autor:
Odabaş, Dursun, Çaksen, Hüseyin *, Şar, Şakir, Tombul, Temel, Kisli, Mesude, Tuncer, Oğuz, Yuca, Köksal, Yılmaz, Cahide
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology 2005 69(7):923-928
Autor:
Schaffer, Ashleigh E, Breuss, Martin W, Caglayan, Ahmet Okay, Al-Sanaa, Nouriya, Al-Abdulwahed, Hind Y, Kaymakçalan, Hande, Yılmaz, Cahide, Zaki, Maha S, Rosti, Rasim O, Copeland, Brett, Baek, Seung Tae, Musaev, Damir, Scott, Eric C, Ben-Omran, Tawfeg, Kariminejad, Ariana, Kayserili, Hulya, Mojahedi, Faezeh, Kara, Majdi, Cai, Na, Silhavy, Jennifer L, Elsharif, Seham, Fenercioglu, Elif, Barshop, Bruce A, Kara, Bulent, Wang, Rengang, Stanley, Valentina, James, Kiely N, Nachnani, Rahul, Kalur, Aneesha, Megahed, Hisham, Incecik, Faruk, Danda, Sumita, Alanay, Yasemin, Faqeih, Eissa, Melikishvili, Gia, Mansour, Lobna, Miller, Ian, Sukhudyan, Biayna, Chelly, Jamel, Dobyns, William B, Bilguvar, Kaya, Jamra, Rami Abou, Gunel, Murat, Gleeson, Joseph G
Publikováno v:
Nature genetics, vol 50, iss 8
Neuronal migration defects, including pachygyria, are among the most severe developmental brain defects in humans. Here, we identify biallelic truncating mutations in CTNNA2, encoding αN-catenin, in patients with a distinct recessive form of pachygy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::068401e6d8c7bcef8afba6331e1ecd0d
https://escholarship.org/uc/item/9s51b96f
https://escholarship.org/uc/item/9s51b96f
Autor:
Başarslan, Fatmagül, Yılmaz, Cahide, Tutanç, Murat, Arıca, Vefik, İnci, Melek, Köksaldı Motor, Vicdan, Bayaroğuları, Hanifi
Suçiçeği, Varicella -zoster virüsünün (VZV) neden olduğu ekzentematöz döküntü ile karakterize bulaşıcı bir hastalıktır. Suçiçeği geçiren hastalarda ensefalit sıklığı %0.1-0.2 olarak belirlenmiştir ve baskılanmış hücresel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4778::e599e02d893a56ad2a9a49f3effab1be
https://hdl.handle.net/20.500.12483/2641
https://hdl.handle.net/20.500.12483/2641
Autor:
Yuca, Sevil Arı1 sevilyuca@yahoo.com, Yılmaz, Cahide2, Cesur, Yaşar1, Doğan, Murat1, Kaya, Avni2, Başaranoğlu, Murat2
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. Dec2010, Vol. 2 Issue 4, p159-163. 5p. 3 Charts, 2 Graphs.
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Akademický článek
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