Erdem Kındış

5PUBLICATIONS
13CO-AUTHORS
Medical infection agents (incl. prions)Developmental genetics (incl. sex determination)Optical technologyMolecular targetsNeonatology
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Publications (5)

|May 18, 2026
Further delineation of the phenotype and genotype in a newly identified PAN2-related disorder.

|Mar 25, 2026
A Case of Restrictive Dermopathy With Atypical Cardiac Anomalies and a Novel ZMPSTE24 Variant.

Erdem Kındış, Ömer Varol

|Aug 05, 2025
Expanding the Genotypic and Phenotypic Spectrum of P3H1 Related Osteogenesis Imperfecta.

Erdem Kındış, Enise Avcı Durmuşaliğlu, Elif Eviz

|Mar 22, 2021
Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features.

Erdem Kındış, Pelin Özlem Simsek-Kiper, Can Koşukcu

|Jul 05, 2020
Poikiloderma with Neutropenia, Clericuzio-Type Accompanied by Loss of Digits Due to Severe Osteomyelitis.

Neslihan Akdogan, Erdem Kindis, Ecem Bostan

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Frequent Collaborators

2 joint publications

Eda Utine

1 joint publications

Neslihan Akdogan

1 joint publications

Ecem Bostan

1 joint publications

Mehmet Alikasifoglu