Showing 1 - 20 results of 28 for search 'Belde Kasap‐Demir', query time: 0.06s
Refine Results
-
1
Awareness of FMF among Caregivers by Belde Kasap Demir, Tuğçe Karahafız, Gülşah Yılmaz, Eren Soyaltın
Published 2021-12-01
Article -
2
-
3
Protracted Febrile Myalgia Associated with Fever of Unknown Origin by Özlem Üzüm, Hayrullah Manyas, Kerem Yıldız, Abbasqulu Baghırov, Belde Kasap-Demir
Published 2020-12-01
Article -
4
A novel OCRL1 gene mutation in a Turkish child with Lowe syndrome by Ali Kanık, Belde Kasap-Demir, Rüya Ateşli, Kayı Eliaçık, Onder Yavaşcan, Mehmet Helvacı
Published 2013-02-01
Article -
5
A Rare Cause of Abdominal Pain and Fever of Unknown Origin: Takayasu Arteritis by Özlem Üzüm, Muhammed Ali Kanık, Kader Vardı, Yeliz Pekçevik, Kayı Eliaçık, Belde Kasap Demir
Published 2019-03-01
Article -
6
-
7
-
8
-
9
-
10
-
11
Known But Forgotten Disease: A Ten-year-old Scurvy Case by Özlem ÜZÜM, İnci Türkan YILMAZ, Ceyda TANRIVERDİ, Fatma Ceren SARIOĞLU, Gülberat İNCE, Belde KASAP-DEMİR, Ali KANIK
Published 2024-04-01
Article -
12
Assessment of Knowledge and Opinions of Family Medicine Residents About the Diagnosis and Treatment of Enuresis in Children by Seçil Arslansoyu Çamlar, Esma Uysal, Eren Soyaltın, Gökçen Erfidan, Demet Alaygut, Fatma Mutlubaş, Hülya Parıldar, Belde Kasap Demir
Published 2021-09-01
Article -
13
-
14
Mutation Analysis of the AGXT Gene in Combined Liver-Kidney and Isolated Liver Transplanted Children for Primary Hyperoxaluria Type 1: a Single Center Experience by Mehmet Turkmen, Demet Alaygut, Sinem Agılkaya, Meral Torun Bayram, Belde Kasap Demir, Alper Soylu, Salih Kavukcu, Sultan Cingoz
Published 2022-10-01
Article -
15
-
16
-
17
-
18
-
19
-
20
A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings by Caner Alparslan, Elif Perihan Öncel, Sinem Akbay, Demet Alaygut, Fatma Mutlubaş, Mansur Tatlı, Martin Konrad, Önder Yavaşcan, Belde Kasap-Demir
Published 2018-02-01
Article