Yayınlar & Eserler

Yayın Ağı
Makaleler 6
Tümü (6)
SCI-E, SSCI, AHCI (6)
SCI-E, SSCI, AHCI, ESCI (6)
Scopus (6)
TRDizin (3)

1. Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

KOTAN L. D., Ternier G., Cakir A. D., EMEKSİZ H. C., TURAN İ., Delpouve G., et al.
GENETICS IN MEDICINE , cilt.23, sa.6, ss.1008-1016, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

2. Clinical characteristics and response to growth hormone treatment in patients with Prader-Willi Syndrome

Evliyaoglu O., Cakir A. D., Bas F., Akin O., ŞIKLAR Z., Ozcabi B., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.423, 2019 (SCI-Expanded, Scopus) identifier

3. Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

ESEN İ., Bayramoglu E., Yildiz M., Aydin M., Ozturhan E. K., Aycan Z., et al.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.11, sa.2, ss.164-172, 2019 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier identifier

4. Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

Poyrazoglu S., Bundak R., Abali Z. Y., Onal H., Sarikaya S., Akgun A., et al.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.10, sa.4, ss.336-342, 2018 (SCI-Expanded, Scopus, TRDizin) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

5. Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation.

Evliyaoğlu O., Ercan O., Ataoğlu E., Zübarıoğlu Ü., Özcabı B., Dağdeviren A., et al.
Journal of clinical research in pediatric endocrinology , cilt.10, sa.2, ss.168-174, 2018 (SCI-Expanded, Scopus, TRDizin) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier identifier

6. Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

Evliyaoglu O., Dokurel I., Bucak F., Ozcabi B., Ercan O., Ceylaner S.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.5, sa.1, ss.55-57, 2013 (SCI-Expanded, Scopus) identifier identifier identifier
Metrikler

Yayın

6

Yayın (WoS)

6

Yayın (Scopus)

6

Atıf (WoS)

66

H-İndeks (WoS)

4

Atıf (Scopus)

71

H-İndeks (Scopus)

5

Açık Erişim

3
BM Sürdürülebilir Kalkınma Amaçları