Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Nida, Dinçel"'
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 11, Iss 1, Pp 23-28 (2021)
Objective: The aim of this study was to determine the relationship between number of passes and complications in pediatric native kidney biopsies performed under ultrasonography guidance. Methods: Forty-nine children who underwent native kidney biops
Externí odkaz:
https://doaj.org/article/563adbd947284847a7acc1ee0f4fe1e9
Autor:
Uğur Seyhan, Betül Pehlivan Zorlu, Özlem Dur, Büşra Koç, Aslı Kantar, Mehmet Coskun, Fatma Devrim, Nida Dinçel
Publikováno v:
Journal of Contemporary Medicine, Vol 11, Iss 2, Pp 244-247 (2021)
Pheochromocytoma is a rare tumor that develops from the chromaffin cells of the sympathetic nervous system. Although hypertension is the most common manifestation of pheochromocytoma, it is less common in children than in adults. This condition may b
Externí odkaz:
https://doaj.org/article/c2303f4f336f4721a92ad54dd86fea44
Autor:
Fatma Devrim, Nida Dinçel
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 10, Iss 2, Pp 170-176 (2020)
INTRODUCTION: Uroflowmetry is an essential noninvasive test with important diagnostic method in patients with initial diagnosis of lower urinary tract dysfunction. We aimed to compare the results of conventional uroflowmetry with those of the new sma
Externí odkaz:
https://doaj.org/article/ca85081e37a54cc8909ec2391f53d658
Publikováno v:
Neuropediatrics.
Background Although it is a valuable option for children with drug-resistant epilepsy, ketogenic diet (KD) therapy is associated with several side effects. The frequency of kidney stones and risk factors for their development in epileptic children re
Autor:
Fatma Devrim, Erkin Serdaroğlu, İlknur Çağlar, Yeliz Oruç, Nevbahar Demiray, Nuri Bayram, Hasan Ağın, Şebnem Çalkavur, Yelda Sorguç, Nida Dinçel, Yüce Ayhan, Ebru Yılmaz, İlker Devrim
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 10, Iss 1, Pp e2018055-e2018055 (2018)
Background: Healthcare–associated infections results increased healthcare costs and mortality. There are limited studies concerning the distribution of the etiologic agents and the resistance patterns of the microorganisms causing healthcare–asso
Externí odkaz:
https://doaj.org/article/aecb773b5b1b4802bf1be2304a5cf114
Autor:
Şükran Keskin Gözmen, Erkin Serdaroğlu, Nida Dinçel, Pınar Erturgut, Cemaliye Başaran, Fatma Devrim, Betül Pehlivan Zorlu, Özlem Dur, Orhan Deniz Kara, Ebru Bekiroğlu Yilmaz
Publikováno v:
Nephrologietherapeutique.
Peritoneal dialysis is the treatment of choice for end-stage renal disease. Peritoneal dialysis related peritonitis is of great importance for patient and technical survival. The aim of our study was to evaluate the accuracy and the correlation betwe
Publikováno v:
Pediatric surgery international. 38(7)
To present baseline characteristics and the long-term treatment results of three groups of patients with idiopathic detrusor overactivity (IDOD) and vesicoureteral reflux (VUR) according to different treatment regimens, which underwent endoscopic sub
Publikováno v:
Journal of Dr. Behcet Uz Children s Hospital.
Objective: The aim of this study was to determine the relationship between number of passes and complications in pediatric native kidney biopsies performed under ultrasonography guidance. Methods: Forty-nine children who underwent native kidney biops
Autor:
Büşra Koç, Fatma Devrim, Nida Dinçel, Aslı Kantar, Uğur Seyhan, Betül Pehlivan Zorlu, Özlem Dur, Mehmet Coskun
Publikováno v:
Volume: 11, Issue: 2 244-247
Journal of Contemporary Medicine
Journal of Contemporary Medicine, Vol 11, Iss 2, Pp 244-247 (2021)
Journal of Contemporary Medicine
Journal of Contemporary Medicine, Vol 11, Iss 2, Pp 244-247 (2021)
Pheochromocytoma is a rare tumor that develops from the chromaffin cells of the sympathetic nervous system. Although hypertension is the most common manifestation of pheochromocytoma, it is less common in children than in adults. This condition may b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1df5d3f357ff1bfba275993239a048f4
https://dergipark.org.tr/tr/pub/jcm/issue/58926/838712
https://dergipark.org.tr/tr/pub/jcm/issue/58926/838712
Publikováno v:
Iranian Journal of Pediatrics.
WOS: 000471326300002
Background: Infantile nephrotic syndrome (INS) refers to disease that is present after the first three months of life up to one year of age. There is genetic heterogeneity and genotype-phenotype correlation is not clear. Obj
Background: Infantile nephrotic syndrome (INS) refers to disease that is present after the first three months of life up to one year of age. There is genetic heterogeneity and genotype-phenotype correlation is not clear. Obj