Search research articles
Contact Us
Filters
Showing results (21-30 of 147) with videos related to
Page
of 15
Sort By:
Pediatric Nephrology (Berlin, Germany)
|
August 23, 2006
Paracellin-1 gene mutation with multiple congenital abnormalities
Mehmet 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WITHDRAWN: TRANSIENT TACHYPNEA OF THE NEWBORN: A PREDICTIVE FACTOR FOR PROLONGED TACHYPNEA
Belde 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 period
Salih Kavukçu, Alper Soylu, Mehmet Türkmen, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 9, 2022
A surprising cause of proteinuria: Questions
Belde 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 mutation
Alper 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 five
Ali 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 group
Demet 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 bladder
Nergis 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 mutations
Hande 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 nephropathy
Demet Alaygut, Meral Torun-Bayram, Alper Soylu, et al.
Page
of 15
Search research articles
Search
Showing results (21-30 of 147) with videos related to
Sort By:
Page
of 15
Pediatric Nephrology (Berlin, Germany)
|
August 23, 2006
Paracellin-1 gene mutation with multiple congenital abnormalities
Mehmet 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 TACHYPNEA
Belde 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 period
Salih Kavukçu, Alper Soylu, Mehmet Türkmen, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 9, 2022
A surprising cause of proteinuria: Questions
Belde 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 mutation
Alper 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 five
Ali 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 group
Demet 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 bladder
Nergis 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 mutations
Hande 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 nephropathy
Demet Alaygut, Meral Torun-Bayram, Alper Soylu, et al.
Page
of 15