Serçin Güven

10PUBLICATIONS
52CO-AUTHORS
Infant and child healthNeonatologyEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesNephrology and urology
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Publications (10)

|Jul 14, 2026
Clinical Characteristics, Genetic Spectrum, and Treatment Outcomes in Children With Primary Hyperoxaluria: Results From a National Turkish Registry.

|Mar 04, 2026
Clinical course of proteinuria due to cubilin variants: a large multicenter pediatric cohort.

Neslihan Cicek, Ceren Alavanda, Ayse Seda Pınarbası

|Dec 20, 2025
Predictors of kidney survival in children with autosomal recessive polycystic kidney disease.

Neslihan Çiçek, İbrahim Gökçe, Ceren Alavanda

|Nov 14, 2025
Benign proximal tubular albuminuria due to AMN mutation: A challenging presentation of Imerslund-Gräsbeck syndrome.

Serim Pul, Serçin Güven, Neslihan Çiçek

|Dec 19, 2024
Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.

Mehmet Eltan, Ceren Alavanda, Zehra Yavas Abali

|Aug 31, 2024
Pediatric crush-related acute kidney injury and risk factors: a single center experience.

Sevgin Taner, Ulas Ozdemir, Tugba Kandemir Gulmez

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Frequent Collaborators

5 joint publications

Serçin Güven

5 joint publications

Ceren Alavanda

5 joint publications

Pınar Ata

5 joint publications

İbrahim Gökçe