Doga Turkkahraman (D Turkkahraman, Doga Turkahraman, Doğa Türkkahraman)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 10

Top Venues

Journal of clinical research in pediatric endocrinology

Journal of pediatric endocrinology & metabolism : JPEM

American journal of medical genetics. Part A

Journal of endocrinological investigation

University of Health Sciences, Antalya Training and Research Hospital

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Health Sciences, Antalya Training and Research Hospital Jun 06 2010

Turkey

Prof. MD. Doga Turkkahraman :: Pediatric Endocrinology

Publications

Doga Turkkahraman, Merve Gullu, Suat Tekin, Tarkan Kalkan
Familial dysalbuminemic hyperthyroxinemia (FDH) due to Arg242 His variant in ALB gene in Turkish children. Journal of pediatric endocrinology & metabolism : JPEM 37 (6) (2024)
Doga Turkkahraman, Merve Gullu, Suat Tekin, Tarkan Kalkan
Familial dysalbuminemic hyperthyroxinemia (FDH) due to Arg242 His variant in ALB gene in Turkish children. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Doga Turkkahraman, Merve Gullu, Suat Tekin, Tarkan Kalkan
Familial dysalbuminemic hyperthyroxinemia (FDH) due to Arg242 His variant in ALB gene in Turkish children. Journal of pediatric endocrinology & metabolism : JPEM 37 (6) (2024)
Suat Tekin, Merve Gullu, Doga Turkkahraman
Late-onset Van Wyk Grumbach syndrome without precocious puberty. Pediatrics international : official journal of the Japan Pediatric Society 65 (1) (2023)
Doga Turkkahraman, Suat Tekin, Merve Gullu, Güzin Aykal
Serum Ghrelin and Glucagon-like Peptide 1 Levels in Children with Prader-Willi and Bardet-Biedl Syndromes Journal of clinical research in pediatric endocrinology 16 (2) (2023)
Doga Turkkahraman, E C Sirazi, Güzin Aykal
Serum alpha-melanocyte-stimulating hormone (a-MSH), brain-derived neurotrophic factor (BDNF), and agouti-related protein (AGRP) levels in children with Prader-Willi or Bardet-Biedl syndromes. Journal of endocrinological investigation 45 (5) (2022)
Doga Turkkahraman, Atiye Nil Palancı Sakarya, Nadide Cemre Randa
A novel EZH2 gene variant in a case of Weaver syndrome with postaxial polydactyly. American journal of medical genetics. Part A 185 (7) (2021)
Doga Turkkahraman, Nimet Karataş Torun, Nadide Cemre Randa
A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene Journal of clinical research in pediatric endocrinology 13 (3) (2020)
Ayşehan Akıncı, Doga Turkkahraman, İbrahim Tekedereli, Leyla Özer, Bahri Evren, Ibrahim Sahin, Tarkan Kalkan, Yusuf Çürek, Emine Çamtosun, Esra Döğer, Aysun Bideci, Ayla Güven, Erdal Eren, Özlem Sangün, Atilla Çayır, Pelin Bilir, Ayça Törel Ergür, Oya Ercan
Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study Journal of clinical research in pediatric endocrinology 11 (4) (2019)
Suheyla Gorar, Doga Turkkahraman, Kanay Yararbas
A Large PROP1 Gene Deletion in a Turkish Pedigree. Case reports in endocrinology 2018 (2018)

Doga Turkkahraman.css-eqlu8i{font-size:small;padding-left:4px;} (D Turkkahraman, Doga Turkahraman, Doğa Türkkahraman)

Publication Activity (10 Years)

Top Topics

Top Venues

Doga Turkkahraman (D Turkkahraman, Doga Turkahraman, Doğa Türkkahraman)