Ayca Dilruba Aslanger

13PUBLICATIONS
76CO-AUTHORS
Adolescent healthDevelopmental genetics (incl. sex determination)Disease surveillanceNeurology and neuromuscular diseasesCondensed matter imaging
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Publications (13)

|Aug 06, 2026
Assessment of cardiometabolic risk using single point insulin sensitivity estimator (SPISE) in pediatric Bardet-Biedl Syndrome: a pilot study.

|Aug 01, 2026
Molecular Analysis of SCN1A Gene Variants Associated with Dravet Syndrome: Implications for Diagnosis and Management.

|Jul 27, 2026
Electroclinical phenotypes-genetic characterization of developmental and epileptic encephalopathies in a cohort study.

|Jul 19, 2026
Clinical and Molecular Characterization of a RASopathy Cohort From Türkiye and an AMMECR1-Related Noonan Syndrome-Mimicking Phenotype.

|Apr 27, 2026
Vanishing White Matter with Cerebral Salt Wasting: A Case Report.

|Jul 23, 2025
Hypohidrotic Ectodermal Dysplasias: Phenotypic and Genotypic Findings in 32 Cases.

Zeynep Esener, Mehmet Akif Yücesoy, Alper Gezdirici

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Frequent Collaborators

4 joint publications

Gözde Yeşil Sayın

3 joint publications

Volkan Karaman

3 joint publications

Güven Toksoy

2 joint publications

Zehra Oya Uyguner