Bilimsel çalışmalar

Uzm. Dr. Serim Pul

15 yayın. Her yayının yanında bilginin kaynağı yazar.

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  1. 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 Açık erişimli tam metinKaynak: ORCID

  2. 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 Kaynak: ORCID

  3. Acute Kidney Injury After Pediatric Hematopoietic Stem Cell Transplantation: Incidence, Risk Factors, and Outcomes

    Pediatric transplantation, 2026

    DOI 10.1111/petr.70405 PMID 42461237 Açık erişimli tam metinKaynak: Europe PMC

  4. Long-term clinical course of pediatric familial Mediterranean fever with heterozygous pathogenic MEFV exon 10 variants

    European Journal of Pediatrics, 2026

    DOI 10.1007/s00431-026-07462-9 PMID 42811127 Kaynak: ORCID

  5. Benign proximal tubular albuminuria due to AMN mutation: A challenging presentation of Imerslund-Gräsbeck syndrome

    Pediatric Nephrology, 2026

    DOI 10.1007/s00467-025-07052-1 PMID 41236624 Açık erişimli tam metinKaynak: ORCID

  6. OP–153 Impaired circadian blood pressure pattern in pediatric alport syndrome: a single-center experience

    BMJ Paediatrics Open, 2026

    DOI 10.1136/bmjpo-2026-epa-unepsa.150 Açık erişimli tam metinKaynak: OpenAlex

  7. Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings

    Journal of clinical research in pediatric endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2024.2024-1-17 PMID 39113392 2 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC

  8. Benign Proximal Tubular Albuminuria due to AMN mutation: A Challenging Presentation of Imerslund-Gräsbeck Syndrome

    2025

    DOI 10.21203/rs.3.rs-6564862/v1 Açık erişimli tam metinKaynak: ORCID

  9. Pediatric kidney care experience after the 2023 Türkiye earthquake

    Nephrology Dialysis Transplantation, 2024

    DOI 10.1093/ndt/gfae033 PMID 38327222 10 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex

  10. Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation

    Turkish Journal of Pediatrics, 2023

    DOI 10.24953/turkjped.2022.288 PMID 37114699 1 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  11. Clinical and genetic characterization of children with cubilin variants

    Pediatric Nephrology, 2023

    DOI 10.1007/s00467-022-05730-y PMID 36112210 10 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

  12. Phenotypic and genotypic characteristics of children with Bartter

    Turkish Journal of Pediatrics, 2022

    DOI 10.24953/turkjped.2021.4697 PMID 36305432 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID

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

    Pediatric Nephrology, 2021

    Kaynak: ORCID

  14. CATASTROPHIC ANTIPHOSPHOLIPIDE SYNDROME ACCOMPANIED WITH DYSREGULATION OF THE COMPLEMENT SYSTEM

    Dspace Repository (Marmara Üniversitesi), 2021

    Kaynak: OpenAlex

  15. THE ROLE OF THE URINARY ANTIMICROBIAL PEPTIDE CATHELICIDIN LEVELS IN EARLY DIAGNOSIS OF URINARY TRACT INFECTION, DIFFERENTIATION OF CYSTITIS-PYELONEPHRITIS AND PREDICTION OF THE RESISTANT MICROORGANISMS

    Dspace Repository (Marmara Üniversitesi), 2017

    Açık erişimli tam metinKaynak: OpenAlex