Etiological, clinical, and laboratory evaluation of congenital hypothyroidism and determination of levothyroxine (LT4) dose at treatment interruption in differentiating permanent v...

por DÜNDAR, İsmail, BÜYÜKAVCI, Mehmet Akif, ÇİFTÇİ, Nurdan
Publicado 2022

46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report

por Çiftci, Nurdan, Kayaş, Leman, Çamtosun, Emine, Akıncı, Ayşehan
Publicado 2022

Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success

por Çamtosun, Emine, Akıncı, Ayşehan, Kayaş, Leman, Çiftci, Nurdan, Tekedereli, İbrahim
Publicado 2023

Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience

por Çamtosun, Emine, Dündar, İsmail, Akıncı, Ayşehan, Kayaş, Leman, Çiftçi, Nurdan
Publicado 2021

Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth

por Dündar, İsmail, Akıncı, Ayşehan, Çamtosun, Emine, Kayaş, Leman, Çiftçi, Nurdan, Özçetin, Erdener
Publicado 2023

Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism

por Çiftci, Nurdan, Akıncı, Ayşehan, Akbulut, Ekrem, Çamtosun, Emine, Dündar, İsmail, Doğan, Mustafa, Kayaş, Leman
Publicado 2023

Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus

por Güven Baysal, Şenay, Çiftci, Nurdan, Dündar, İsmail, Büyükavcı, Mehmet Akif, Yağın, Fatma Hilal, Çamtosun, Emine, Gümüş Doğan, Derya, Akıncı, Ayşehan
Publicado 2023