Ibrahim Gokce

9PUBLICATIONS
79CO-AUTHORS
Infant and child healthNeonatologyCellular immunologyEpigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)
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Publications (9)

|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

|Jan 31, 2025
Listeria Meningitis as an Indication of Undiagnosed Primary Immune Deficiency, Activated Phosphoinositide 3-Kinase Delta Syndrome: A Case Report.

Pinar Canizci Erdemli, Sevliya Öcal Demir, Selcen Bozkurt

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

Mehmet Eltan, Ceren Alavanda, Zehra Yavas Abali

|Dec 02, 2023
Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil?

Neslihan Günay, İsmail Dursun, İbrahim Gökçe

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