Paediatric Neurology

Uzm. Dr. Serim Pul

Doctor and researcher Ümraniye Eğitim ve Araştırma Hastanesi İstanbul
Proteinuria
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Person ↔ Disease

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  • SpecialtyPaediatric Neurologysaglik.gov.trFrom source
  • Department name at the sourceÇocuk Nörolojisaglik.gov.trFrom source
  • InstitutionÜmraniye Eğitim ve Araştırma Hastanesisaglik.gov.trFrom source
  • Area of workProteinuriaExtracted from 3 publications · Model version —From source
  • Publications15 publicationsORCID, Europe PMC, OpenAlexFrom source
  • ORCID0000-0001-6896-404XORCIDFrom source
  • Last synchronised5 November 2026 08:56https://umraniyeah.saglik.gov.tr/TR-1512997/doktorlarimiz.html#serim-pulsaglik.gov.tr

Scientific work

Publications on Proteinuria

15 publications

  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 Open-access full textSource: 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 Source: 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 Open-access full textSource: 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 Source: 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 Open-access full textSource: 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 Open-access full textSource: 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 citations (Europe PMC) Open-access full textSource: 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 Open-access full textSource: ORCID

  9. Pediatric kidney care experience after the 2023 Türkiye earthquake

    Nephrology Dialysis Transplantation, 2024

    DOI 10.1093/ndt/gfae033 PMID 38327222 10 citations (Europe PMC) Open-access full textSource: 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 citation (Europe PMC) Open-access full textSource: ORCID

View all 15 publications