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American Journal of Medical Genetics. Part A|October 21, 2022
A novel MTX2 gene splice site variant resulting in exon skipping, causing the recently described mandibuloacral dysplasia progeroid syndromeBurcu Yeter Doğan, Neslihan Günay, Yasin Ada, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|March 5, 2020
Calcified renal artery aneurism in the right kidney causing hypertensionNeslihan Günay, Ayşe Seda Pınarbaşı, İsmail Dursun, et al.
Pediatric Nephrology (Berlin, Germany)|January 18, 2021
Do children with solitary or hypofunctioning kidney have the same prevalence for masked hypertension?Sibel Yel, Neslihan Günay, Ayşe Seda Pınarbaşı, et al.
Fetal and Pediatric Pathology|September 7, 2019
Patient Outcomes of Henoch-Schönlein Purpura Nephritis According to the New Semiquantitative ClassificationSibel Yel, Ismail Dursun, Ayşe Seda Pinarbaşi, et al.
Blood Purification|March 30, 2021
Erythropoietin Resistance Index and the Affecting Factors in Children with Peritoneal DialysisAyşe Seda Pınarbaşı, Ismail Dursun, Neslihan Günay, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|January 14, 2020
Epidermolysis bullosa complicated with nephrotic syndrome due to AA amyloidosis: A case report and brief review of literatureAyşe Seda Pınarbaşı, Ismail Dursun, Burcu Daldaban, et al.
European Journal of Pediatrics|May 12, 2023
Clinical usefulness of anti-nuclear antibody in childhood: real-world experience at a tertiary care center : Usefulness of ANA in pediatric autoimmune diseasesNihal Şahin, Ayşenur Paç Kısaarslan, Sümeyra Özdemir Çiçek, et al.
Pediatric Nephrology (Berlin, Germany)|October 12, 2025
Multicenter evaluation of ambulatory blood pressure in children with CAKUT: distinctive profiles in the cystic dysplasia subgroupSibel Yel, Neslihan Günay, Pelin Abdal Yıldırım, et al.
Turkish Journal of Medical Sciences|June 27, 2021
A nationwide retrospective study in Turkish children with nephrocalcinosisSerra Sürmeli Döven, Sebahat Tülpar, Funda Baştuğ, et al.
Pediatric Nephrology (Berlin, Germany)|December 2, 2023
Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil?Neslihan Günay, İsmail Dursun, İbrahim Gökçe, et al.
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