Makaleler
Tümü (6)
SCI-E, SSCI, AHCI (6)
SCI-E, SSCI, AHCI, ESCI (6)
Scopus (6)
TRDizin (3)
2021
20211. 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)
2019
20192. 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)
2019
20193. 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)
2018
20184. 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)
2018
20185. 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)
2013
20136. 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)