Pınar Ata

Akademik Profiller

1. 1
   Clinical and genetic characterization of children with cubilin variantsPediatric Nephrology
   2023
2. 2
   First Patient Diagnosed as Feingold Syndrome Type 2 with Alport Syndrome and Review of the Current LiteratureMolecular Syndromology
   2022
3. 3
   Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the LiteratureCalcified Tissue International
   2021
4. 4
   Biallelic Mutations in DNAJB11are Associated with Prenatal Polycystic Kidney Disease in a Turkish FamilyMolecular Syndromology
   2021
5. 5
   Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) MutationHormone Research in Paediatrics
   2020
6. 6
   Novel mutations and deletions in cystic fibrosis in a tertiary cystic fibrosis center in IstanbulPediatric Pulmonology
   2019
7. 7
   Association between occurrence of ossicular chain defect and osteoprotegerin gene expression in patients with chronic otitis mediaEuropean Archives of Oto-Rhino-Laryngology
   2019
8. 8
   Challenges in the treatment of fibrodysplasia ossificans progressivaRheumatology International
   2018
9. 9
   Intraoperative Tissue-Immunosuppressive Therapy Reduces Rejection Episodes in Heart Transplant RecipientsExperimental and Clinical Transplantation
   2018

Yayın listesi ORCID kaydından alındı.