Murat Karaoglan
12PUBLICATIONS
16CO-AUTHORS
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Publications (12)
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|Jun 24, 2025
Genotype-Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency Using Next Generation Sequencing.Nurgul Atas, Murat Karaoglan, Gülper Nacarkahya
|Sep 07, 2024
Allergic reactions to enzyme replacement therapy in children with lysosomal storage diseases and their management.Elif Arik, Özlem Keskin, Serpil Albayrak
|May 03, 2024
Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia.Murat Karaoglan, Gulper Nacarkahya, Emel Hatun Aytac
|Mar 07, 2021
Challenges of CYP21A2 genotyping in children with 21-hydroxylase deficiency: determination of genotype-phenotype correlation using next generation sequencing in Southeastern Anatolia.M Karaoğlan, G Nacarkahya, E H Aytaç
|Dec 05, 2020
Immunological interpretation of minipuberty: Minipuberty as the driving force of sexual dimorphism in the immune response.Murat Karaoglan, Gulper Nacarkahya
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Frequent Collaborators
3 joint publications
Gulper Nacarkahya
3 joint publications
Mehmet Keskin
2 joint publications
Ozlem Keskin
1 joint publications
Emel Hatun Aytac
1 joint publications
Elif Arik
1 joint publications
Serpil Albayrak
1 joint publications
Mahmut Cesur
1 joint publications
Gaye Inal
1 joint publications
Ahmet Yildirim
1 joint publications
Ercan Kucukosmanoglu