Ceren Alavanda
11PUBLICATIONS
47CO-AUTHORS
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Publications (11)
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|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
|Feb 04, 2025
Identification of Novel Variants in the NHS in Four Turkish Patients With Nance-Horan Syndrome.Ceren Alavanda, Esra Arslan Ateş, Şenol Demir
|Jan 06, 2025
Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in TürkiyeÖmer Doğru, Ceren Alavanda, Şenol Demir
|Dec 19, 2024
Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.Mehmet Eltan, Ceren Alavanda, Zehra Yavas Abali
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Frequent Collaborators
6 joint publications
Pınar Ata
5 joint publications
Sercin Guven
5 joint publications
Ibrahim Gokce
4 joint publications
Serçin Güven
4 joint publications
Serim Pul
3 joint publications
Nurdan Yıldız
2 joint publications
Esra Arslan Ates
2 joint publications
Mehtap Kaya
2 joint publications
Özde Nisa Türkkan
2 joint publications
Şenol Demir
