Zobrazeno 1 - 10
of 22
pro vyhledávání: '"İbrahim Gökçe"'
Autor:
İbrahim Gökçe, Neslihan Çiçek, Serçin Güven, Ülger Altuntaş, Neşe Bıyıklı, Nurdan Yıldız, Harika Alpay
Publikováno v:
Balkan Medical Journal, Vol 34, Iss 5, Pp 432-435 (2017)
Background: The causative agent spectrum and resistance patterns of urinary tract infections in children are affected by many factors. Aims: To demonstrate antibiotic resistance in urinary tract infections and changing ratio in antibiotic resistance
Externí odkaz:
https://doaj.org/article/4e03dccbecf8457a8d64500dbb8c5e7a
Publikováno v:
Balkan Medical Journal, Vol 28, Iss 02, Pp 222-223 (2011)
Protracted febrile myalgia (PFM) is a rare form of vasculitic disease which is an uncommon dramatic manifestation of familial Mediterranean fever (FMF), characterized by severe crippling myalgia and high fever. We describe a 14-year-old boy who prese
Externí odkaz:
https://doaj.org/article/37cb1a63af88430485719e9a3d64123a
Autor:
Serçin, Güven, İbrahim, Gökçe, Ceren, Alavanda, Burcu, Öztürk Hişmi, Neslihan, Çiçek, Ece, Bodur Demirci, Mehtap, Sak, Nurdan, Yıldız, Pınar, Ata, Harika, Alpay
Publikováno v:
Turkish Archives of Pediatrics. 57:432-440
Objective: We aimed to present the characteristics, genetic analysis results, long-term prognosis of our patients with distal kidney tubular acidosis, and the relationship between hyperammonemia and distal kidney tubular acidosis. Materials and Metho
Autor:
Seda SARIKAYA, Halil İbrahim GÖKÇE
Publikováno v:
Veterinary Journal of Mehmet Akif Ersoy University. 6:133-138
Bu çalışma ile feline calicivirus (FCV) ile enfekte kedilerde hücresel immün yanıtın, oksidatif stresin ve yangısal sürecin belirlenmesi amaçlanmıştır. Çalışmada FCV ile enfekte 20 adet kedi ve 10 adet klinik olarak sağlıklı olmak
Autor:
Funda Baştuğ, Ayşe Ağbaş, Sebahat Tülpar, Zeynep Nagehan Yürük Yıldırım, Neslihan Çiçek, Neslihan Günay, Atilla Gemici, Binnaz Çelik, Emine Özlem Çam Delebe, Hülya Nalçacıoğlu, Alev Yılmaz, İbrahim Gökçe, Gülay Demircin, Duygu Övünç Hacıhamdioğlu, Kenan Yılmaz, Bahriye Atmış, Esra Karabağ Yılmaz, Pelin Ertan, İsmail Dursun, Bağdagül Aksu, Burcu Bulum Akbulut, Serra Sürmeli Döven, Nimet Öner, Sibel Yel, Ahmet Midhat Elmacı, Yeşim Özdemir Atikel, Gökçen Erfidan, Berfin Uysal, Neşe Bıyıklı, Burcu Yazıcıoğlu, Nuran Küçük, Elif Çomak, Fatma Lale Sever, İpek Akil, Özlem Aksoy, Harika Alpay
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.We evaluated the demographic features, etiologic risk factors, treatment strategies, and outcome of the infants and children with urolithiasis (U
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4c64e2e95b8d1482226de65ff443d04
https://hdl.handle.net/11424/289564
https://hdl.handle.net/11424/289564
Publikováno v:
Journal of Experimental and Basic Medical Sciences. 1:147-158
Publikováno v:
Volume: 7, Issue: 3 155-160
Veterinary Journal of Mehmet Akif Ersoy University
Mehmet Akif Ersoy Üniversitesi Veteriner Fakültesi Dergisi
Veterinary Journal of Mehmet Akif Ersoy University
Mehmet Akif Ersoy Üniversitesi Veteriner Fakültesi Dergisi
The aims of the present study was to determine whether or not abomasal damages occurs in calves with abdominal distention using by plasma pepsinogen levels and the positivity of the fecal occult blood test (FOBT). In the study, 30 calves with abdomin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4de37f6dcff1b9007615ddc62db94fc
https://dergipark.org.tr/tr/pub/maeuvfd/issue/73681/1110471
https://dergipark.org.tr/tr/pub/maeuvfd/issue/73681/1110471
Autor:
Serçin Güven, İbrahim Gökçe, Ceren Alavanda, Neslihan Çiçek, Ece Bodur Demirci, Mehtap Sak, Serim Pul, Özde Nisa Türkkan, Nurdan Yıldız, Pınar Ata, Harika Alpay
Publikováno v:
Web of Science
Introduction. Bartter syndrome (BS) is a group of autosomal-recessive tubular disorders and it is classified into five genetic subtypes. BS can also be classified by phenotype (antenatal, classic). Patients with mutations in the same gene can present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28558ebd3f92bd7f22e117848f9bf0d4
https://hdl.handle.net/11424/282848
https://hdl.handle.net/11424/282848
Autor:
Serim Pul, İbrahim Gökçe, Ece Demirci Bodur, Serçin Güven, Neslihan Çiçek, Mehtap Sak, Özde Nisa Türkkan, Deniz Filinte, Cemile Pehlivanoğlu, Betül Sözeri, Harika Alpay
Publikováno v:
The Turkish Journal of Pediatrics. 65:330
Background. Antiphospholipid syndrome (APS), particularly the catastrophic antiphospholipid syndrome (CAPS), is one of the rare causes of thrombotic microangiopathy (TMA). CAPS is the most severe form of APS, especially when accompanied by complement
Publikováno v:
Mehmet Akif Ersoy Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi.