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Demet Alaygut

Showing results (61-70 of 97) with videos related to

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The Turkish Journal of Pediatrics|October 17, 2018
A rare cause of neonatal hypertension: Congenital mesoblastic nephromaEren Soyaltın, Demet Alaygut, Caner Alparslan, et al.
Klinische Padiatrie|September 20, 2024
10 Years of Antenatal Hydronephrosis Experience: Comparing Two Different GuidelinesEsra Ensari, Onder Yavascan, Caner Alparslan, et al.
Pediatric Reports|December 22, 2022
Evaluation of Pediatric Patients with a Diagnosis of UreteroceleÖzgür Özdemir Şimşek, Sibel Tiryaki, Gökçen Erfidan, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 16, 2021
Is coronavirus pandemic-related anxiety higher in children with chronic kidney disease than healthy children?Gökçen Erfidan, Gonca Özyurt, Seçil Arslansoyu-Çamlar, et al.
Biochemical Genetics|April 24, 2016
Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of TurkeyCan Huzmeli, Ferhan Candan, Demet Alaygut, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 21, 2019
Adolescents with unexplained chest pain reported depression and impaired emotional and social functioningKayi Eliacik, Nurullah Bolat, Ali Kanik, et al.
The Turkish Journal of Pediatrics|August 14, 2018
A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblingsCaner Alparslan, Elif Perihan Öncel, Sinem Akbay, et al.
Clinical Rheumatology|June 3, 2017
Frequency of familial Mediterranean fever (MEFV) gene mutations in patients with biopsy-proven primary glomerulonephritisCan Huzmeli, Ferhan Candan, Gokhan Bagci, et al.
Turkish Archives of Pediatrics|February 3, 2022
Prediction of More Severe MEFV Gene Mutations in ChildhoodSeviye Güneş-Yılmaz, Belde Kasap-Demir, Eren Soyaltın, et al.
Turkish Journal of Medical Sciences|December 14, 2020
Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experienceBelde Kasap Demir, Fatma Mutlubaş, Eren Soyaltın, et al.
Pageof 10

Showing results (61-70 of 97) with videos related to

Sort By:
Pageof 10
The Turkish Journal of Pediatrics|October 17, 2018
A rare cause of neonatal hypertension: Congenital mesoblastic nephromaEren Soyaltın, Demet Alaygut, Caner Alparslan, et al.
Klinische Padiatrie|September 20, 2024
10 Years of Antenatal Hydronephrosis Experience: Comparing Two Different GuidelinesEsra Ensari, Onder Yavascan, Caner Alparslan, et al.
Pediatric Reports|December 22, 2022
Evaluation of Pediatric Patients with a Diagnosis of UreteroceleÖzgür Özdemir Şimşek, Sibel Tiryaki, Gökçen Erfidan, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 16, 2021
Is coronavirus pandemic-related anxiety higher in children with chronic kidney disease than healthy children?Gökçen Erfidan, Gonca Özyurt, Seçil Arslansoyu-Çamlar, et al.
Biochemical Genetics|April 24, 2016
Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of TurkeyCan Huzmeli, Ferhan Candan, Demet Alaygut, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 21, 2019
Adolescents with unexplained chest pain reported depression and impaired emotional and social functioningKayi Eliacik, Nurullah Bolat, Ali Kanik, et al.
The Turkish Journal of Pediatrics|August 14, 2018
A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblingsCaner Alparslan, Elif Perihan Öncel, Sinem Akbay, et al.
Clinical Rheumatology|June 3, 2017
Frequency of familial Mediterranean fever (MEFV) gene mutations in patients with biopsy-proven primary glomerulonephritisCan Huzmeli, Ferhan Candan, Gokhan Bagci, et al.
Turkish Archives of Pediatrics|February 3, 2022
Prediction of More Severe MEFV Gene Mutations in ChildhoodSeviye Güneş-Yılmaz, Belde Kasap-Demir, Eren Soyaltın, et al.
Turkish Journal of Medical Sciences|December 14, 2020
Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experienceBelde Kasap Demir, Fatma Mutlubaş, Eren Soyaltın, et al.
Pageof 10