Bilimsel çalışmalar

Prof. Dr. Rezan Topaloğlu

308 yayın. Her yayının yanında bilginin kaynağı yazar.

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  1. COVID-19 IN PEDIATRIC NEPHROLOGY CENTERS IN TURKEY

    Pediatric Nephrology, 2021

    2 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  2. NEPHROTIC SYNDROME WITH MUTATION IN SPHINGOSINE-1-PHOSPHATE LYASE: 6 CASES

    2021

    Kaynak: OpenAlex

  3. EFFECTS OF RAAS INHIBITION AND IMMUNOSUPPRESSIVE THERAPY IN PEDIATRIC PATIENTS WITH X-LINKED ALPORT SYNDROME

    Çanakkale Onsekiz Mart University AVESIS, 2021

    Kaynak: OpenAlex

  4. TÜRKİYE'DE ÇOCUK NEFROLOJİ MERKEZLERİNDE COVID-19

    Çanakkale Onsekiz Mart University AVESIS, 2021

    Kaynak: OpenAlex

  5. Development and testing of an artificial intelligence tool for predicting end-stage kidney disease in patients with immunoglobulin A nephropathy

    Kidney International, 2020

    DOI 10.1016/j.kint.2020.07.046 PMID 32889014 73 atıf (Europe PMC) Kaynak: OpenAlex

  6. Updating the International IgA Nephropathy Prediction Tool for use in children

    Kidney International, 2020

    DOI 10.1016/j.kint.2020.10.033 PMID 33220356 59 atıf (Europe PMC) Kaynak: OpenAlex

  7. Improving treatment decisions using personalized risk assessment from the International IgA Nephropathy Prediction Tool

    Kidney International, 2020

    DOI 10.1016/j.kint.2020.04.042 PMID 32464215 44 atıf (Europe PMC) Kaynak: OpenAlex

  8. Clinical practice recommendations for recurrence of focal and segmental glomerulosclerosis/steroid‐resistant nephrotic syndrome

    Pediatric Transplantation, 2020

    DOI 10.1111/petr.13955 PMID 33378587 25 atıf (Europe PMC) Kaynak: OpenAlex

  9. Promoting Breastfeeding and Interaction of Pediatric Associations With Providers of Nutritional Products

    Frontiers in Pediatrics, 2020

    DOI 10.3389/fped.2020.562870 PMID 33324589 11 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  10. Clinical characteristics of children with congenital anomalies of the kidney and urinary tract and predictive factors of chronic kidney disease

    The Turkish Journal of Pediatrics, 2020

    DOI 10.24953/turkjped.2020.05.005 PMID 33108076 9 atıf (Europe PMC) Kaynak: OpenAlex

  11. COL4A3 mutation is an independent risk factor for poor prognosis in children with Alport syndrome

    Pediatric Nephrology, 2020

    DOI 10.1007/s00467-020-04574-8 PMID 32394188 12 atıf (Europe PMC) Kaynak: OpenAlex

  12. Cystinosis beyond kidneys: gastrointestinal system and muscle involvement

    BMC Gastroenterology, 2020

    DOI 10.1186/s12876-020-01385-x PMID 32727395 12 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  13. Transplantation in pediatric aHUS within the era of eculizumab therapy

    Pediatric Transplantation, 2020

    DOI 10.1111/petr.13914 PMID 33217100 2 atıf (Europe PMC) Kaynak: OpenAlex

  14. P1809EARLY URINARY SYSTEM COMPLICATIONS IN CHILDREN WITH HEMATOPOIETIC STEM CELL TRANSPLANTATION

    Nephrology Dialysis Transplantation, 2020

    DOI 10.1093/ndt/gfaa142.p1809 Kaynak: OpenAlex

  15. P1825ANALYSIS OF LATE RENAL COMPLICATIONS AND RISK FACTORS IN CHILDREN WITH HEMATOPOIETIC STEM CELL TRANSPLANTATION

    Nephrology Dialysis Transplantation, 2020

    DOI 10.1093/ndt/gfaa142.p1825 Kaynak: OpenAlex

  16. P0063CLINICAL CHARACTERISTICS OF PATIENTS WITH GENETICALLY CONFIRMED ALPORT SYNDROME

    Nephrology Dialysis Transplantation, 2020

    DOI 10.1093/ndt/gfaa142.p0063 Kaynak: OpenAlex

  17. Predictors for the use of herbal and dietary supplements in children and adolescents with kidney and urinary tract diseases

    European Journal of Pediatrics, 2020

    DOI 10.1007/s00431-020-03757-7 PMID 32761383 Kaynak: OpenAlex

  18. Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis

    Kidney International, 2019

    DOI 10.1016/j.kint.2019.09.026 PMID 31959358 47 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  19. Management of bone disease in cystinosis: Statement from an international conference

    Journal of Inherited Metabolic Disease, 2019

    DOI 10.1002/jimd.12134 PMID 31177550 41 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  20. Growth Patterns After Kidney Transplantation in European Children Over the Past 25 Years: An ESPN/ERA-EDTA Registry Study

    Transplantation, 2019

    DOI 10.1097/tp.0000000000002726 PMID 30946218 26 atıf (Europe PMC) Kaynak: OpenAlex

  21. Sex and age as determinants for high blood pressure in pediatric renal transplant recipients: a longitudinal analysis of the CERTAIN Registry

    Pediatric Nephrology, 2019

    DOI 10.1007/s00467-019-04395-4 PMID 31811541 17 atıf (Europe PMC) Kaynak: OpenAlex

  22. Rituximab for Children With Difficult-to-Treat Nephrotic Syndrome: Its Effects on Disease Progression and Growth

    Frontiers in Pediatrics, 2019

    DOI 10.3389/fped.2019.00313 PMID 31417883 11 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  23. Psychiatric morbidity and different treatment modalities in children with chronic kidney disease

    Archives de Pédiatrie, 2019

    DOI 10.1016/j.arcped.2019.05.013 PMID 31278026 12 atıf (Europe PMC) Kaynak: OpenAlex

  24. Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in the asymptomatic period: effects of early initiation of CoQ10 supplementation

    The Turkish Journal of Pediatrics, 2019

    DOI 10.24953/turkjped.2019.05.003 PMID 32104996 16 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  25. Clinical and histopathological prognostic factors affecting the renal outcomes in childhood ANCA-associated vasculitis

    Pediatric Nephrology, 2019

    DOI 10.1007/s00467-018-4162-5 PMID 30607566 13 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  26. Do not Miss Rare and Treatable Cause of Early-Onset Hemolytic Uremic Syndrome: Cobalamin C Deficiency

    The Nephron journals/Nephron journals, 2019

    DOI 10.1159/000497822 PMID 31137025 6 atıf (Europe PMC) Kaynak: OpenAlex

  27. CD 80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood

    Pediatrics International, 2019

    DOI 10.1111/ped.14005 PMID 31513327 11 atıf (Europe PMC) Kaynak: OpenAlex

  28. The European Society for Paediatric Nephrology study of pediatric renal care in Europe: comparative analysis 1998–2017

    Pediatric Nephrology, 2019

    DOI 10.1007/s00467-019-04378-5 PMID 31664556 13 atıf (Europe PMC) Kaynak: OpenAlex

  29. Surgical management of renovascular hypertension in children and young adults: a 13-year experience

    Interactive Cardiovascular and Thoracic Surgery, 2019

    DOI 10.1093/icvts/ivz157 PMID 31651975 4 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  30. BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immuneosseous- dysplasia

    The Turkish Journal of Pediatrics, 2019

    DOI 10.24953/turkjped.2019.01.018 PMID 31559731 3 atıf (Europe PMC) Kaynak: OpenAlex

  31. A rare cause of steroid-resistant nephrotic syndrome in a child: Answers

    Pediatric Nephrology, 2019

    DOI 10.1007/s00467-019-04385-6 PMID 31811537 Kaynak: OpenAlex

  32. A rare cause of steroid resistant nephrotic syndrome in a child: Questions

    Pediatric Nephrology, 2019

    DOI 10.1007/s00467-019-04381-w PMID 31811535 Kaynak: OpenAlex

  33. Is there long-term value of pathology scoring in immunoglobulin A nephropathy? A validation study of the Oxford Classification for IgA Nephropathy (VALIGA) update

    Nephrology Dialysis Transplantation, 2018

    DOI 10.1093/ndt/gfy302 PMID 30418652 81 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  34. Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study

    Transplantation, 2018

    DOI 10.1097/tp.0000000000002414 PMID 30130322 56 atıf (Europe PMC) Kaynak: OpenAlex

  35. Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

    The Journal of Pediatrics, 2018

    DOI 10.1016/j.jpeds.2018.03.052 PMID 29753540 39 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  36. Outcome of renal transplantation in small infants: a match-controlled analysis

    Pediatric Nephrology, 2018

    DOI 10.1007/s00467-018-3895-5 PMID 29536257 17 atıf (Europe PMC) Kaynak: OpenAlex

  37. Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation

    Pediatric Neurology, 2018

    DOI 10.1016/j.pediatrneurol.2018.07.008 PMID 30337132 24 atıf (Europe PMC) Kaynak: OpenAlex

  38. JC polyomavirus replication and associated disease in pediatric renal transplantation: an international CERTAIN Registry study

    Pediatric Nephrology, 2018

    DOI 10.1007/s00467-018-4029-9 PMID 30058047 12 atıf (Europe PMC) Kaynak: OpenAlex

  39. FP755EUROPEAN SOCIETY OF PAEDIATRIC NEPHROLOGY (ESPN) STUDY OF PAEDIATRIC RENAL CARE IN EUROPE: COMPARATIVE ANALYSIS 1998 - 2017

    Nephrology Dialysis Transplantation, 2018

    DOI 10.1093/ndt/gfy104.fp755 Kaynak: OpenAlex

  40. CLINICAL AND PATHOLOGIC CHARACTERISTICS OF GENETICALLY CONFIRMED ALPORT SYNDROME PATIENTS

    2018

    Kaynak: OpenAlex

  41. Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

    Nature Genetics, 2017

    DOI 10.1038/ng.3933 PMID 28805828 184 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  42. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment

    Pediatric Nephrology, 2017

    DOI 10.1007/s00467-017-3634-3 PMID 28337616 55 atıf (Europe PMC) Kaynak: OpenAlex

  43. The Clinical and Mutational Spectrum of Turkish Patients with Cystinosis

    Clinical Journal of the American Society of Nephrology, 2017

    DOI 10.2215/cjn.00180117 PMID 28793998 16 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  44. Dyslipidemia after pediatric renal transplantation—The impact of immunosuppressive regimens

    Pediatric Transplantation, 2017

    DOI 10.1111/petr.12914 PMID 28370750 15 atıf (Europe PMC) Kaynak: OpenAlex

  45. Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one

    Pediatric Rheumatology, 2017

    DOI 10.1186/s12969-017-0141-9 Kaynak: OpenAlex

  46. Incomplete vaccination coverage in European children with end-stage kidney disease prior to renal transplantation

    Pediatric Nephrology, 2017

    DOI 10.1007/s00467-017-3776-3 PMID 28983694 14 atıf (Europe PMC) Kaynak: OpenAlex

  47. Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis

    Clinical Immunology, 2017

    DOI 10.1016/j.clim.2017.10.010 PMID 29107076 7 atıf (Europe PMC) Kaynak: OpenAlex

  48. Predictors of methotrexate response in Turkish children with oligoarticular and polyarticular juvenile idiopathic arthritis

    The Turkish Journal of Pediatrics, 2017

    DOI 10.24953/turkjped.2017.01.002 PMID 29168357 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  49. Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

    Proceedings of the National Academy of Sciences, 2016

    DOI 10.1073/pnas.1612594113 PMID 27559085 211 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  50. Risk factors for progression in children and young adults with IgA nephropathy: an analysis of 261 cases from the VALIGA European cohort

    Pediatric Nephrology, 2016

    DOI 10.1007/s00467-016-3469-3 PMID 27557557 75 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex