Wissenschaftliche Arbeiten

Uzm. Dr. Özde Nisa Türkkan

62 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  1. Awareness, perceptions, and practices regarding transition to adult care for nephropathic cystinosis in Türkiye: a nationwide cross-sectional survey of pediatric nephrologists

    Orphanet Journal of Rare Diseases, 2026

    DOI 10.1186/s13023-026-04557-2 PMID 42881396 Frei zugänglicher VolltextQuelle: OpenAlex

  2. Clinical course of proteinuria due to cubilin variants: a large multicenter pediatric cohort

    Pediatric Nephrology, 2026

    DOI 10.1007/s00467-026-07227-4 PMID 41781699 Frei zugänglicher VolltextQuelle: ORCID

  3. Predictors of kidney survival in children with autosomal recessive polycystic kidney disease

    Clinical and Experimental Nephrology, 2026

    DOI 10.1007/s10157-025-02801-w PMID 41420720 Quelle: ORCID

  4. Follow-up of Pediatric Patients With Renovascular Hypertension in Türkiye

    Research Square, 2026

    DOI 10.21203/rs.3.rs-8786518/v1 Frei zugänglicher VolltextQuelle: OpenAlex

  5. Additional file 1 of Awareness, perceptions, and practices regarding transition to adult care for nephropathic cystinosis in Türkiye: a nationwide cross-sectional survey of pediatric nephrologists

    Figshare, 2026

    DOI 10.6084/m9.figshare.34558226 Frei zugänglicher VolltextQuelle: OpenAlex

  6. Does cytoreductive surgery and hyperthermic intraperitoneal chemotherapy improve survival in children with desmoplastic small round cell tumors? First experiences from Turkey

    Marmara medical journal, 2025

    DOI 10.5472/marumj.1627763 Frei zugänglicher VolltextQuelle: OpenAlex

  7. First Results of the European Cystinuria Registry

    Journal of the American Society of Nephrology, 2025

    DOI 10.1681/asn.2025bdqnghxs Quelle: OpenAlex

  8. The relationship between urine heat shock protein 70 and congenital anomalies of the kidney and urinary tract: UTILISE study

    Frontiers in Urology, 2024

    DOI 10.3389/fruro.2023.1281081 PMID 40778050 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  9. Pediatric kidney care experience after the 2023 Türkiye earthquake

    Nephrology Dialysis Transplantation, 2024

    DOI 10.1093/ndt/gfae033 PMID 38327222 10 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  10. Pediatri Polikliniklerinde Sık Görülen Vakalar

    Akademisyen Kitabevi eBooks, 2023

    DOI 10.37609/akya.2508 Frei zugänglicher VolltextQuelle: OpenAlex

  11. Urine soluble TLR4 levels may contribute to predict urinary tract infection in children: the UTILISE Study

    Pediatric Nephrology, 2023

    DOI 10.1007/s00467-023-06063-0 PMID 37462743 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  12. Çocuklarda Hipertansiyon Risk Faktörü Olarak Obezite ve Metabolik Sendrom

    OSMANGAZİ JOURNAL OF MEDICINE, 2023

    DOI 10.20515/otd.1344723 Frei zugänglicher VolltextQuelle: ORCID

  13. A RARE ASSOCIATION OF PROPIONIC ACIDEMIA AND NEPHROLITHIASIS

    Pediatric Nephrology, 2023

    Quelle: ORCID

  14. Association between serum biomarkers and oral health status in children with chronic kidney disease: A cross-sectional study

    Clinical Oral Investigations, 2023

    DOI 10.1007/s00784-023-04989-1 PMID 37014503 11 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  15. CLINICAL PROGRESS AND PROGNOSIS IN C3 GLOMERULOPAYHY

    Pediatric Nephrology, 2023

    Quelle: ORCID

  16. Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation

    Turkish Journal of Pediatrics, 2023

    DOI 10.24953/turkjped.2022.288 PMID 37114699 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  17. Clinical and genetic characterization of children with cubilin variants

    Pediatric Nephrology, 2023

    DOI 10.1007/s00467-022-05730-y PMID 36112210 10 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  18. EVALUATION OF CONGENITAL NEPHROGENIC DIABETES INSIPIDUS CASES WITH AVPR2 MUTATION: A SINGLE CENTER EXPERIENCE

    Pediatric Nephrology, 2023

    Quelle: ORCID

  19. Urinary HSP70 improves diagnostic accuracy for urinary tract infection in children: UTILISE study

    Pediatric Nephrology, 2022

    DOI 10.1007/s00467-022-05664-5 PMID 35849222 7 Zitationen (Europe PMC) Quelle: OpenAlex

  20. A CASE OF C3 GLOMERULOPATHY PRESENTING WITH HENOCH-SCHoNLEIN PURPURA-LIKE CLINIC

    Pediatric Nephrology, 2022

    Quelle: ORCID

  21. A LATE ONSET UVEITIS AFTER TUBULOINTERTITIAL NEPHRITIS AND UVEIT (TINU) SYNDROME

    Pediatric Nephrology, 2022

    Quelle: ORCID

  22. A RARE HISTOPATHOLOGY: GRANULOMATOUS BK VIRUS NEPHROPATHY

    Pediatric Nephrology, 2022

    Quelle: ORCID

  23. CLINICAL SPECTRUM OF CUBULIN MUTATIONS

    Pediatric Nephrology, 2022

    Quelle: ORCID

  24. COULD NEUTROPHIL-LYMPHOCYTE RATIO BE USED AS A PROGNOSTIC FACTOR IN HEMOLYTIC UREMIC SYNDROME?

    Pediatric Nephrology, 2022

    Quelle: ORCID

  25. DIFFICULT CASES OF PERITONITIS WITH UNUSUAL MICROORGANISMS IN CHILDREN WITH PERITONEAL DIALYSIS

    Pediatric Nephrology, 2022

    Quelle: ORCID

  26. DOES COVID-19 FACILITATE NEW-ONSET DIABETES MELLITUS AFTER TRANSPLANTATION

    Pediatric Nephrology, 2022

    Quelle: ORCID

  27. EARLY HIGH-DOSE STEROID TREATMENT IS LIFE-SAVING IN RITUXIMAB-RELATED ACUTE LUNG INJURY

    Pediatric Nephrology, 2022

    Quelle: ORCID

  28. GENETIC TESTS IN NON-NEUROGENIC NEUROGENIC BLADDER: TWO SIBLINGS WITH OCHOA SYNDROME

    Pediatric Nephrology, 2022

    Quelle: ORCID

  29. NEUTROPHIL-TO-LYMPHOCYTE AND PLATELET-TO-LYMPHOCYTE RATIO IN PERITONEAL DIALYSIS ASSOCIATED PERITONITIS IN PEDIATRIC PATIENTS

    Pediatric Nephrology, 2022

    Quelle: ORCID

  30. PERITONITIS AND URINARY TRACT INFECTIONS FOLLOWING INTRAVESICAL BOTULINUM TOXIN INJECTION IN CHILDREN ON PERITONEAL DIALYSIS: CASE REPORT

    Pediatric Nephrology, 2022

    Quelle: ORCID

  31. POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME (PRES) AND ASSOCIATION WITH COVID-19

    Pediatric Nephrology, 2022

    Quelle: ORCID

  32. Phenotypic and genotypic characteristics of children with Bartter

    Turkish Journal of Pediatrics, 2022

    DOI 10.24953/turkjped.2021.4697 PMID 36305432 3 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  33. RECURRENT ACUTE KIDNEY INJURY DUE TO THROMBOSIS OF THE VENA CAVA INFERIOR

    Pediatric Nephrology, 2022

    Quelle: ORCID

  34. URINARY HSP70 IMPROVES DIAGNOSTIC ACCURACY FOR URINARY TRACT INFECTION IN CHILDREN: UTILISE STUDY

    Pediatric Nephrology, 2022

    Quelle: ORCID

  35. URINARY SYSTEM INVOLVEMENT IN MUCOPOLYSACCHARIDOSIS DISEASE: TWO CASES WITH CHRONIC KIDNEY DISEASE

    Pediatric Nephrology, 2022

    Quelle: ORCID

  36. USING CORTICOSTEROIDS IN THE TREATMENT OF ACUTE TUBULAR NECROSIS: EFFECTIVE OR NOT?

    Pediatric Nephrology, 2022

    Quelle: ORCID

  37. Vascular endothelial dysfunction in renal replacement therapy modalities

    Revista de Nefrologia, Dialisis Y Transplante, 2022

    Quelle: ORCID

  38. Rituximab treatment for difficult-to-treat nephrotic syndrome in children: a multicenter, retrospective study

    TURKISH JOURNAL OF MEDICAL SCIENCES, 2021

    DOI 10.3906/sag-2012-297 PMID 33581711 4 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  39. ANXIETY, DEPRESSION AND COPING OF CHILDREN WITH CHRONIC KIDNEY DISEASE AND THEIR CAREGIVERS DURING THE COVID-19 PANDEMIC

    Pediatric Nephrology, 2021

    Quelle: ORCID

  40. CHARACTERISTICS OF PATIENTS WITH DISTAL RENAL TUBULAR ACIDOSIS AND ITS ASSOCIATION WITH HYPERAMMONEMIA: A SINGLE-CENTER EXPERIENCE

    Pediatric Nephrology, 2021

    Quelle: ORCID

  41. CLINICAL-GENETIC CHARACTERISTICS AND PREDICTORS OF DISEASE PROGRESSION IN PATIENTS WITH AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

    Pediatric Nephrology, 2021

    Quelle: ORCID

  42. COVID-19 DISEASE IN PEDIATRIC NEPHROLOGY PATIENTS- A SINGLE CENTER EXPERIENCE

    Pediatric Nephrology, 2021

    Quelle: ORCID

  43. Differential diagnosis of classical Bartter syndrome and Gitelman syndrome: Do we need genetic analysis?

    Marmara Medical Journal, 2021

    DOI 10.5472/marumj.1012351 Frei zugänglicher VolltextQuelle: ORCID

  44. KIDNEY DIMENSION IS THE MOST IMPORTANT PARAMETER ASSOCIATED WITH DETERIORATION IN KIDNEY FUNCTION IN CHILDREN WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE

    Pediatric Nephrology, 2021

    Quelle: ORCID

  45. PHENOTYPIC AND GENOTYPIC CHARACTERISTICS OF CHILDREN WITH BARTTER SYNDROME

    Pediatric Nephrology, 2021

    Quelle: ORCID

  46. Nephroprotective Therapies: Complementary and Alternative Medicine

    Journal of Literature Pharmacy Sciences, 2021

    DOI 10.5336/pharmsci.2020-76002 Frei zugänglicher VolltextQuelle: OpenAlex

  47. Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype

    European Journal of Medical Genetics, 2020

    DOI 10.1016/j.ejmg.2019.01.011 PMID 30682496 10 Zitationen (Europe PMC) Quelle: ORCID

  48. RESULTS OF URINE DIPSTICK SCREENING TEST IN ELEMENTARY SCHOOL CHILDREN

    İstanbul Tıp Fakültesi Dergisi, 2020

    DOI 10.26650/iuitfd.2019.0037 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

  49. Akut Poststreptokoksik Glomerülonefrite Bağlı Gelişen Hızlı İlerleyici Glomerülonefrit

    Çocuk Dergisi / Journal of Child, 2019

    DOI 10.5222/j.child.2019.82574 Frei zugänglicher VolltextQuelle: OpenAlex

  50. RITUXIMAB TREATMENT FOR DIFFICULT-TO-TREAT NEPHROTIC SYNDROME IN CHILDREN: A MULTICENTER STUDY

    Trakya University's Institutional Open Access System (Trakya University), 2018

    Frei zugänglicher VolltextQuelle: OpenAlex