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Belde Kasap

Showing results (21-30 of 147) with videos related to

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Pediatric Nephrology (Berlin, Germany)|August 23, 2006
Paracellin-1 gene mutation with multiple congenital abnormalitiesMehmet Türkmen, Belde Kasap, Alper Soylu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 25, 2009
WITHDRAWN: TRANSIENT TACHYPNEA OF THE NEWBORN: A PREDICTIVE FACTOR FOR PROLONGED TACHYPNEABelde Kasap, Nuray Duman, Esra Ozer, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 2004
Two-hour post-dose cyclosporin A levels in adolescent renal transplant recipients in the late post-transplant periodSalih Kavukçu, Alper Soylu, Mehmet Türkmen, et al.
Pediatric Nephrology (Berlin, Germany)|January 9, 2022
A surprising cause of proteinuria: QuestionsBelde Kasap Demir, Ali Kanık, Melis Köse, et al.
Seminars in Arthritis and Rheumatism|January 15, 2008
Protracted febrile myalgia syndrome in a patient with familial Mediterranean fever homozygous for the E148Q mutationAlper Soylu, Belde Kasap, Mehmet Türkmen, et al.
International Journal of Pediatric Otorhinolaryngology|May 2, 2022
A comparative study for the clinical features in children with PFAPA syndrome who were diagnosed before and after the age of fiveAli Kanık, Kayı Eliaçık, Esra Toprak Kanık, et al.
Urology|May 17, 2013
The relationships between renal compensatory hypertrophy etiologic factors and anthropometric development in the pediatric age groupDemet Alaygut, Alper Soylu, Belde Kasap, et al.
Pediatric Nephrology (Berlin, Germany)|December 31, 2005
In vitro analysis of the effect of hyperbilirubinemia on rabbit ureter and bladderNergis Murat, Belde Kasap, Salih Kavukcu, et al.
Clinical Rheumatology|November 28, 2025
Validity of the Eurofever/PRINTO genetic FMF classification criteria in FMF and PFAPA patients carrying non-confirmatory MEFV gene mutationsHande Ilgaz Tüzen, Yeşim Yardımcı, Seviye Güneş Yılmaz, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Chronic kidney disease in an adolescent with hyperuricemia: familial juvenile hyperuricemic nephropathyDemet Alaygut, Meral Torun-Bayram, Alper Soylu, et al.
Pageof 15

Showing results (21-30 of 147) with videos related to

Sort By:
Pageof 15
Pediatric Nephrology (Berlin, Germany)|August 23, 2006
Paracellin-1 gene mutation with multiple congenital abnormalitiesMehmet Türkmen, Belde Kasap, Alper Soylu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 25, 2009
WITHDRAWN: TRANSIENT TACHYPNEA OF THE NEWBORN: A PREDICTIVE FACTOR FOR PROLONGED TACHYPNEABelde Kasap, Nuray Duman, Esra Ozer, et al.
Pediatric Nephrology (Berlin, Germany)|April 1, 2004
Two-hour post-dose cyclosporin A levels in adolescent renal transplant recipients in the late post-transplant periodSalih Kavukçu, Alper Soylu, Mehmet Türkmen, et al.
Pediatric Nephrology (Berlin, Germany)|January 9, 2022
A surprising cause of proteinuria: QuestionsBelde Kasap Demir, Ali Kanık, Melis Köse, et al.
Seminars in Arthritis and Rheumatism|January 15, 2008
Protracted febrile myalgia syndrome in a patient with familial Mediterranean fever homozygous for the E148Q mutationAlper Soylu, Belde Kasap, Mehmet Türkmen, et al.
International Journal of Pediatric Otorhinolaryngology|May 2, 2022
A comparative study for the clinical features in children with PFAPA syndrome who were diagnosed before and after the age of fiveAli Kanık, Kayı Eliaçık, Esra Toprak Kanık, et al.
Urology|May 17, 2013
The relationships between renal compensatory hypertrophy etiologic factors and anthropometric development in the pediatric age groupDemet Alaygut, Alper Soylu, Belde Kasap, et al.
Pediatric Nephrology (Berlin, Germany)|December 31, 2005
In vitro analysis of the effect of hyperbilirubinemia on rabbit ureter and bladderNergis Murat, Belde Kasap, Salih Kavukcu, et al.
Clinical Rheumatology|November 28, 2025
Validity of the Eurofever/PRINTO genetic FMF classification criteria in FMF and PFAPA patients carrying non-confirmatory MEFV gene mutationsHande Ilgaz Tüzen, Yeşim Yardımcı, Seviye Güneş Yılmaz, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Chronic kidney disease in an adolescent with hyperuricemia: familial juvenile hyperuricemic nephropathyDemet Alaygut, Meral Torun-Bayram, Alper Soylu, et al.
Pageof 15