Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Exercise performance in children and adolescents with cystic fibrosis with and without abnormal glucose tolerance: a single center cross-sectional study

Kocaaga E., Inal-Ince D., Dogru D., ALİKAŞİFOĞLU A., Ademhan-Tural D., Bozdemir-Ozel C., et al.
PHYSIOTHERAPY THEORY AND PRACTICE , cilt.40, sa.2, ss.230-240, 2024 (SCI-Expanded) identifier identifier identifier

Alterations in insulin-like growth factor system in spinal muscular atrophy

YEŞBEK KAYMAZ A., Bal S. K., Bora G., TALİM B., Ozon A., ALİKAŞİFOĞLU A., et al.
MUSCLE & NERVE , cilt.66, sa.5, ss.631-638, 2022 (SCI-Expanded) identifier identifier identifier

Feminizing Adrenocortical Tumors as a Rare Etiology of Isosexual/Contrasexual Pseudopuberty

VURALLI KARAOĞLAN D., Gonc N., Ozon A., EKİNCİ S., Dogan H. S., TEKGÜL S., et al.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.14, sa.1, ss.17-28, 2022 (SCI-Expanded) Creative Commons License identifier identifier identifier identifier

Management of prolactinomas in children and adolescents; which factors define the response to treatment?

ALİKAŞİFOĞLU A., ÇELİK ERTAŞ N. B., ÖZÖN Z. A., GÖNÇ E. N., KANDEMİR N.
PITUITARY , cilt.25, sa.1, ss.167-179, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Sleep disordered breathing in patients with Prader willi syndrome: Impact of underlying genetic mechanism

Ozsezen B., EMİRALİOĞLU N., Ozon A., Akin O., Tural D. A., SUNMAN B., et al.
RESPIRATORY MEDICINE , cilt.187, 2021 (SCI-Expanded) identifier identifier identifier

Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism

GÜNBEY C., Ozon A., GÖNÇ E. N., ALİKAŞİFOĞLU A., KARAHAN S., KANDEMİR N.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.13, sa.3, ss.269-275, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier identifier

Cardiovascular risk factors in adolescents with type 1 diabetes: Prevalence and gender differences

VURALLI KARAOĞLAN D., Jalilova L., ALİKAŞİFOĞLU A., ÖZÖN Z. A., GÖNÇ E. N., KANDEMİR N.
HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.236, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier

Epidemiology of type 1 diabetes in children and adolescents: a 50-year, single center experience

KANDEMİR N., VURALLI KARAOĞLAN D., ÖZÖN Z. A., GÖNÇ E. N., ARDIÇLI D., Jalilova L., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.99, 2021 (SCI-Expanded) identifier

Clinical features and long-term follow up of childhood papillary thyroid cancer (PTC): a single reference-center experience

Ozon A., Emet D. C., Gonc N., VURALLI KARAOĞLAN D., Buyukyilmaz G., KANDEMİR N., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.62-63, 2021 (SCI-Expanded) identifier

Is conventional treatment still the first choice in pediatric patients with PHEX mutations in an era of monoclonal FGF-23 antibody?

Alikasifoglu A., Unsal Y., Gonc N., Ozon A., Kandemir N., Alikasifoglu M.
HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.210-211, 2021 (SCI-Expanded) identifier

Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation

ALİKAŞİFOĞLU A., ÜNSAL Y., GÖNÇ E. N., ÖZÖN Z. A., KANDEMİR N., ALİKAŞİFOĞLU M.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.34, sa.12, ss.1573-1584, 2021 (SCI-Expanded) identifier identifier identifier

Approach to pheochromocytoma and paraganglioma in children and adolescents: A retrospective clinical study from a tertiary care center

ARDIÇLI B., USER İ. R., ÇİFTÇİ A. Ö., AKYÜZ C., KUTLUK M. T., Gonc N., et al.
JOURNAL OF PEDIATRIC UROLOGY , cilt.17, sa.3, 2021 (SCI-Expanded) identifier identifier identifier

Adrenocortical tumours in children: a review of surgical management at a tertiary care centre.

ARDIÇLI B., USER İ. R., ÇİFTÇİ A. Ö., AKYÜZ C., KUTLUK M. T., YALÇIN B., et al.
ANZ journal of surgery , cilt.91, sa.5, ss.992-999, 2021 (SCI-Expanded) identifier identifier identifier

Which parameters predict the beneficial effect of GnRHa treatment on height in girls with central precocious puberty?

VURALLI KARAOĞLAN D., Gonc N. E., ÖZÖN Z. A., KANDEMİR N., ALİKAŞİFOĞLU A.
CLINICAL ENDOCRINOLOGY , cilt.94, sa.5, ss.804-810, 2021 (SCI-Expanded) identifier identifier identifier

Alpha-Melanocyte-Stimulating Hormone is Elevated in Hypothalamic Obesity Associated with Childhood Craniopharyngioma

Emet D. C., Ozon A., ALİKAŞİFOĞLU A., KANDEMİR N., Gonc N.
OBESITY , cilt.29, sa.2, ss.402-408, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Obstructive sleep apnea in children with hypothalamic obesity: Evaluation of possible related factors

İYİGÜN İ., ALİKAŞİFOĞLU A., Gonc N., Ozon A., Eryilmaz Polat S., Hizal M., et al.
PEDIATRIC PULMONOLOGY , cilt.55, sa.12, ss.3532-3540, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Novel insights into diabetes mellitus due toDNAJC3-defect: Evolution of neurological and endocrine phenotype in the pediatric age group

ÖZÖN Z. A., ALİKAŞİFOĞLU A., KANDEMİR N., Aydin B., GÖNÇ E. N., KARAOSMANOĞLU B., et al.
PEDIATRIC DIABETES , cilt.21, sa.7, ss.1176-1182, 2020 (SCI-Expanded) identifier identifier identifier

Gender-related differences in etiology of organic central precocious puberty

VURALLI KARAOĞLAN D., Ozon A., GÖNÇ E. N., Oguz K. K., KANDEMİR N., ALİKAŞİFOĞLU A.
TURKISH JOURNAL OF PEDIATRICS , cilt.62, sa.5, ss.763-769, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

Central nervous system imaging in girls with central precocious puberty: when is necessary?

VURALLI KARAOĞLAN D., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N., ÖZÖN Z. A.
ARCHIVES OF ENDOCRINOLOGY METABOLISM , cilt.64, sa.5, ss.591-596, 2020 (SCI-Expanded) identifier identifier identifier

Physical activity, functional capacity, and anaerobic power in cystic fibrosis with and without impaired glucose tolerance

Kocaaga E., Inal-Ince D., Ademhan-Tural D., Bozdemir-Ozel C., Calik-Kutukcu E., Vardar-Yagli N., et al.
EUROPEAN RESPIRATORY JOURNAL , cilt.56, 2020 (SCI-Expanded) identifier

Oral health and halitosis among type 1 diabetic and healthy children

Iscan T. A., ÖZŞİN ÖZLER C., İLERİ KEÇELİ T., Guciz-Dogan B., ALİKAŞİFOĞLU A., UZAMIŞ TEKÇİÇEK M.
JOURNAL OF BREATH RESEARCH , cilt.14, sa.3, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose?

VURALLI KARAOĞLAN D., ALİKAŞİFOĞLU A., İYİGÜN İ., Canoruc D., Ozon A., Gonc N., et al.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.12, sa.1, ss.37-44, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations

Fu J., Korwutthikulrangsri M., GÖNÇ E. N., Sillers L., Liao X., ALİKAŞİFOĞLU A., et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.105, sa.3, 2020 (SCI-Expanded) Creative Commons License identifier identifier identifier

Long-term effects of GnRH agonist treatment on body mass index in girls with idiopathic central precocious puberty

VURALLI KARAOĞLAN D., ÖZÖN Z. A., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.33, sa.1, ss.99-105, 2020 (SCI-Expanded) identifier identifier identifier

Spondyloocular syndrome: Presentation of two siblings diagnosed with the rare disease and the results of Pamidronate Therapy

VURALLI KARAOĞLAN D., ŞİMŞEK KİPER P. Ö., Utine E., ÜNSAL Y., ALİKAŞİFOĞLU A., KANDEMİR N.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.387, 2019 (SCI-Expanded) identifier

Improvement of final height in idiopathic central precocious puberty is associated with delay of bone maturation with GnRH agonist therapy under the age of 7 years

VURALLI KARAOĞLAN D., GÖNÇ E. N., ÖZÖN Z. A., KANDEMİR N., ALİKAŞİFOĞLU A.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.330, 2019 (SCI-Expanded) identifier

To whom should central nervous system imaging be performed in girls with central precocious puberty (CPP)?

VURALLI KARAOĞLAN D., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N., ÖZÖN Z. A.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.465, 2019 (SCI-Expanded) identifier

Long term effects of GnRH agonist therapy on BMI in girls with idiopathic central precocious puberty

VURALLI KARAOĞLAN D., ÖZÖN Z. A., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.464, 2019 (SCI-Expanded) identifier

Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome

Simsek-Kiper P. O., Taskiran E., KOŞUKCU C., ARSLAN U. E., Cormier-Daire V., Gonc N., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.179, sa.7, ss.1157-1172, 2019 (SCI-Expanded) Creative Commons License identifier identifier identifier

Can having a sibling with type 1 diabetes cause disordered eating behaviors?

AKGÜL S., ALİKAŞİFOĞLU A., Ozon A., Gonc N., Duzceker Y., Ors S., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.31, sa.7, ss.711-716, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

What Is the Best Parameter to Decide the Initial Dose of Depot Leuprolide Acetate in Girls with Idiopathic Central Precocious Puberty?

VURALLI KARAOĞLAN D., ALİKAŞİFOĞLU A., Lyigun I., Canoruc D., Ozon A., Gonc N., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.102-103, 2018 (SCI-Expanded) identifier

Gender-Related Differences in Etiological Distribution of Organic Causes of Central Precocious Puberty

VURALLI KARAOĞLAN D., Ozon A., Gonc N., KANDEMİR N., ALİKAŞİFOĞLU A.
HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.518-519, 2018 (SCI-Expanded) identifier

Hyperinsulinemic Hypoglycemia in Congenital Disorder of Glycosylation Type-1a (CDG-1a)

Vuralli D., YILDIZ Y., SİVRİ H. S., ALİKAŞİFOĞLU A.
HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.362-363, 2018 (SCI-Expanded) identifier

Early Onset GH Replacement in GH Deficiency: Is Neonatal Hypoglycemia Important for Long Term Follow-up?

ALİKAŞİFOĞLU A., CANORUÇ EMET S. D., Ozon A., Gonc N., KANDEMİR N.
HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.386, 2018 (SCI-Expanded) identifier

The Frequency of Obstructive Sleep Apnea in Children with Hypothalamic and Exogenous Obesity

İYİGÜN İ., ALİKAŞİFOĞLU A., Ozon A., Gonc N., Hizal M., Eryilmaz S., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.303-304, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma identifier

A Rare Cause of Hyperinsulinemic Hypoglycemia: Costello Syndrome

VURALLI KARAOĞLAN D., KOŞUKCU C., Taskiran E., Simsek P. O., ÜTİNE G. E., BODUROĞLU O. K., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.363, 2018 (SCI-Expanded) identifier

Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy

GÖNÇ E. N., Ozon A., ALİKAŞİFOĞLU A., KANDEMİR N.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, sa.3, ss.283-287, 2017 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

Clinical and laboratory parameters predicting a requirement for the reevaluation of growth hormone status during growth hormone treatment Retesting early in the course of GH treatment

Vuralli D., GÖNÇ E. N., ÖZÖN Z. A., ALİKAŞİFOĞLU A., KANDEMİR N.
GROWTH HORMONE & IGF RESEARCH , cilt.34, ss.31-37, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency

KHATTAB A., Haider S., KUMAR A., DHAWAN S., ALAM D., Romero R., et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.114, sa.10, 2017 (SCI-Expanded) identifier

A pheochromocytoma case diagnosed as adrenal incidentaloma

VURALLI D., KANDEMİR N., Clark G., ORHAN D., ALİKAŞİFOĞLU A., Gonc N., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.59, sa.2, ss.200-206, 2017 (SCI-Expanded) Creative Commons License identifier identifier identifier

Novel and prevalent CYP11B1 gene mutations in Turkish patients with 11-beta hydroxylase deficiency

KANDEMİR N., Yilmaz D. Y., GÖNÇ E. N., Ozon A., ALİKAŞİFOĞLU A., DURSUN A., et al.
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY , cilt.165, ss.57-63, 2017 (SCI-Expanded) identifier identifier identifier

SOX9 GENE DUPLICATION-RELATED 46, XX OVOTESTICULAR DISORDER OF SEX DEVELOPMENT

Ozon A., ALİKAŞİFOĞLU A., Gonc N., Vuralli D., Buyukyilmaz G., Kiper O. P. S., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.371, 2017 (SCI-Expanded) identifier

ESTABLISHMENT OF HORMONE CONTROL WITH DEXAMETHASONE IN PATIENTS WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIA AFTER FINAL HEIGHT

Gonc N., Ozon A., ALİKAŞİFOĞLU A., VURALLI KARAOĞLAN D., KANDEMİR N.
HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.252, 2017 (SCI-Expanded) identifier

HYPERCALCEMIA DEVELOPING IN THREE CASES FOLLOWING DISCONTINUATION OF DENOSUMAB TREATMENT

ÖZÖN Z. A., Buyukyilmaz G., ALİKAŞİFOĞLU A., GÖNÇ E. N., KURUCU N., AKYÜZ C.
HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.452, 2017 (SCI-Expanded) identifier

Results of intraoperative gamma probe survey and frozen section in surgical treatment of parathyroid adenoma in children

SOYER T., KARNAK İ., TUNCEL M., EKİNCİ S., Andiran F., ÇİFTÇİ A. Ö., et al.
JOURNAL OF PEDIATRIC SURGERY , cilt.51, sa.9, ss.1492-1495, 2016 (SCI-Expanded) identifier identifier identifier

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome.

VURALLı D., Gönç N., VIDAUD D., OZON A., ALIKASIFOGLU A., KANDEMIR N.
Journal of clinical research in pediatric endocrinology , cilt.8, ss.96-100, 2016 (SCI-Expanded) Creative Commons License identifier identifier identifier

An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto Thyroiditis

Kizilkan M. P., KANBUR N., AKGÜL S., ALİKAŞİFOĞLU A.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.8, sa.1, ss.92-95, 2016 (SCI-Expanded) Creative Commons License identifier identifier identifier

Development of Type 1 Diabetes in a Child with Inherited CD59 Deficiency Treated with Eculizumab

KOCA S. B., Ozon A., ALİKAŞİFOĞLU A., Haliloglu G., Topaloglu H.
HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.201, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma identifier

A Nonvirilized form of Classic 3 beta-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria

ALİKAŞİFOĞLU A., Buyukyilmaz G., GÖNÇ E. N., ÖZÖN Z. A., KANDEMİR N., DÜNDAR M., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.281, 2016 (SCI-Expanded) identifier

Hyperthyroidism After Allogeneic Hematopoietic Stem Cell Transplantation: A Report of Four Cases

SAĞ E., Gonc N., ALİKAŞİFOĞLU A., Kuskonmaz B. B., Uckan D., Ozon A., et al.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.4, ss.349-354, 2015 (SCI-Expanded) Creative Commons License identifier identifier identifier

Prevalence of nasal carriage of methicillin-resistant Staphylococcus aureus in children with diabetes mellitus: Trends between 2005 and 2013

KARADAG-ONCEL E., Gonc N., ALTAY O., CENGİZ A. B., Ozon A., PINAR A., et al.
AMERICAN JOURNAL OF INFECTION CONTROL , cilt.43, sa.9, ss.1015-1017, 2015 (SCI-Expanded) identifier identifier identifier

Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene

ALİKAŞİFOĞLU A., Vuralli D., Hiort O., Gonc N., Ozon A., KANDEMİR N.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.3, ss.249-252, 2015 (SCI-Expanded) Creative Commons License identifier identifier identifier

Evaluation of hypothalamic-pituitary function in children following acute bacterial meningitis

Karadag-Oncel E., Cakir M., KARA A., Gonc N., CENGİZ A. B., Ozon A., et al.
PITUITARY , cilt.18, sa.1, ss.1-7, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Changing Etiological Trends in Male Precocious Puberty: Evaluation of 100 Cases with Central Precocious Puberty over the Last Decade

ALİKAŞİFOĞLU A., Vuralli D., GÖNÇ E. N., Ozon A., KANDEMİR N.
HORMONE RESEARCH IN PAEDIATRICS , cilt.83, sa.5, ss.340-344, 2015 (SCI-Expanded) Creative Commons License identifier identifier identifier

Variable Phenotype of Diabetes Mellitus in Siblings with a Homozygous PTF1A Enhancer Mutation

GÖNÇ E. N., Ozon A., ALİKAŞİFOĞLU A., HALİLOĞLU M., Ellard S., Shaw-Smith C., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.84, sa.3, ss.206-211, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Clinical characteristics of type 1 diabetes over a 40 year period in Turkey: secular trend towards earlier age of onset

ARDIÇLI D., KANDEMİR N., ALİKAŞİFOĞLU A., Ozon A., Gonc N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.27, ss.635-641, 2014 (SCI-Expanded) identifier identifier identifier

Need for Comprehensive Hormonal Workup in the Management of Adrenocortical Tumors in Children

GÖNÇ E. N., ÖZÖN Z. A., Cakir M. D., ALİKAŞİFOĞLU A., KANDEMİR N.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.6, sa.2, ss.68-73, 2014 (SCI-Expanded) Creative Commons License identifier identifier identifier

Carotid intima media thickness in adolescents with increased risk for atherosclerosis

ERKOÇOĞLU M., ozön z. a., GÖÇMEN R., ALİKAŞİFOĞLU A., GÖNÇ E. N., KANDEMİR N.
Turkish Journal Of Pediatrics , cilt.5, ss.510-518, 2013 (SCI-Expanded) identifier identifier identifier

Thyroid hormone resistance: a novel mutation in thyroid hormone receptor beta (THRB) gene - case report

Isik E., Beck-Peccoz P., Campi I., ÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.55, sa.3, ss.322-327, 2013 (SCI-Expanded) identifier identifier identifier

Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency

KANDEMİR N., VURALLI KARAOĞLAN D., Taskiran E., Gonc N., Ozon A., ALİKAŞİFOĞLU A., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.54, sa.6, ss.570-575, 2012 (SCI-Expanded) identifier identifier identifier

17 beta-Hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17 beta HSD3 gene

ALİKAŞİFOĞLU A., Hiort O., Gonc N., DEMİRBİLEK H., Isik E., KANDEMİR N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.25, ss.561-563, 2012 (SCI-Expanded) identifier identifier identifier

Evaluation of serum kisspeptin levels in girls in the diagnosis of central precocious puberty and in the assessment of pubertal suppression

DEMİRBİLEK H., GÖNÇ E. N., Ozon A., ALİKAŞİFOĞLU A., KANDEMİR N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.25, ss.313-316, 2012 (SCI-Expanded) identifier identifier identifier

Hypophosphatasia Presenting with Pyridoxine-Responsive Seizures, Hypercalcemia, and Pseudotumor Cerebri: Case Report

DEMİRBİLEK H., Alanay Y., ALİKAŞİFOĞLU A., TOPÇU M., Mornet E., Gonc N., et al.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.4, sa.1, ss.34-38, 2012 (SCI-Expanded) Creative Commons License identifier identifier identifier

Assessment of gonadotrophin suppression in girls treated with GnRH analogue for central precocious puberty; validity of single luteinizing hormone measurement after leuprolide acetate injection

DEMİRBİLEK H., ALİKAŞİFOĞLU A., Gonc N. E., Ozon A., KANDEMİR N.
CLINICAL ENDOCRINOLOGY , cilt.76, sa.1, ss.126-130, 2012 (SCI-Expanded) identifier identifier identifier

Is basal serum 17-OH progesterone a reliable parameter to predict nonclassical congenital adrenal hyperplasia in premature adrenarche?

GÖNÇ E. N., ÖZÖN Z. A., ALİKAŞİFOĞLU A., ENGIZ O., Bulum B., KANDEMİR N.
TURKISH JOURNAL OF PEDIATRICS , cilt.53, sa.3, ss.274-280, 2011 (SCI-Expanded) identifier identifier identifier

GnRH stimulation Test in precocious puberty: Single sample is adequate for diagnosis and dose adjustment

KANDEMİR N., DEMİRBİLEK H., ÖZÖN Z. A., Gönç N., ALİKAŞİFOĞLU A.
JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.3, sa.1, ss.12-17, 2011 (SCI-Expanded) Creative Commons License identifier identifier identifier

Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient

Gonc N., Engiz O., Neumann H. P. H., DEMİRBİLEK H., Ozon A., ALİKAŞİFOĞLU A., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.24, ss.109-112, 2011 (SCI-Expanded) identifier identifier identifier

Pros of priming in the diagnosis of growth hormone deficiency

GÖNÇ E. N., Ozon A., ALİKAŞİFOĞLU A., KANDEMİR N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.24, ss.9-11, 2011 (SCI-Expanded) identifier identifier identifier

Neuroendocrine immune system in familial Mediterranean fever

TOPALOĞLU R., BİLGİNER Y., ALİKAŞİFOĞLU A., ÖZALTIN F., BEŞBAŞ N., ÖZEN S., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.52, sa.6, ss.588-593, 2010 (SCI-Expanded) identifier identifier identifier

Growth hormone deficiency due to traumatic brain injury in a patient with X-linked congenital adrenal hypoplasia

Engiz O., Ozon A., Riepe F., ALİKAŞİFOĞLU A., Gonc N., Kandemir N.
TURKISH JOURNAL OF PEDIATRICS , cilt.52, sa.3, ss.312-316, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Low cortisol levels in active juvenile idiopathic arthritis.

BILGINER Y., TOPALOGLU R., ALIKASIFOGLU A., KARA N., BEŞBAŞ N., Ozen S., et al.
Clinical rheumatology , cilt.29, ss.309-14, 2010 (SCI-Expanded) identifier identifier identifier

The relationship between serum adiponectin, tumor necrosis factor-alpha, leptin levels and insulin sensitivity in childhood and adolescent obesity: Adiponectin is a marker of metabolic syndrome

ALİKAŞİFOĞLU A., GÖNÇ E. N., ÖZÖN Z. A., Şen Y., KANDEMİR N.
JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.1, sa.5, ss.233-239, 2009 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier

Assessment of thyroid function during the long course of Hashimoto's thyroiditis in children and adolescents

DEMİRBİLEK H., KANDEMİR N., GÖNÇ E. N., Ozon A., ALİKAŞİFOĞLU A.
CLINICAL ENDOCRINOLOGY , cilt.71, sa.3, ss.451-454, 2009 (SCI-Expanded) identifier identifier identifier

Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes

Simsek P. O., ÜTİNE G. E., ALİKAŞİFOĞLU A., ALANAY Y., BODUROĞLU O. K., Kandemir N.
TURKISH JOURNAL OF PEDIATRICS , cilt.51, sa.3, ss.294-297, 2009 (SCI-Expanded) identifier identifier identifier

Single sample during gonadotropin stimulation test is adequate for the diagnosis of precocious puberty

KANDEMİR N., DEMİRBİLEK H., Ozon A., Gonc N., ALİKAŞİFOĞLU A.
HORMONE RESEARCH , cilt.72, ss.336, 2009 (SCI-Expanded) identifier

The metabolic risk status in non-obese prepubertal children born small for gestational age

Gumus P., KORKMAZ TOYGAR A., ALİKAŞİFOĞLU A.
HORMONE RESEARCH , cilt.72, ss.439, 2009 (SCI-Expanded) identifier

Cyclic pamidronate treatment in Bruck syndrome: Proposal of a new modality of treatment

Andiran N., ALİKAŞİFOĞLU A., ALANAY Y., YORDAM N.
PEDIATRICS INTERNATIONAL , cilt.50, sa.6, ss.836-838, 2008 (SCI-Expanded) identifier identifier identifier

Final Heights of Boys with Normal Growth Hormone Responses to Provocative Tests Following Priming

GÖNÇ E. N., KANDEMİR N., Ozon A., ALİKAŞİFOĞLU A.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.21, sa.10, ss.963-971, 2008 (SCI-Expanded) identifier identifier identifier

Prevalence and risk factors of metabolic syndrome in obese children and adolescents: the role of the severity of obesity

Sen Y., KANDEMİR N., ALİKAŞİFOĞLU A., Gonc N., Ozon A.
EUROPEAN JOURNAL OF PEDIATRICS , cilt.167, sa.10, ss.1183-1189, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Cyclic pamidronate therapy in children with osteogenesis imperfecta: Results of treatment and follow-up after discontinuation

Andiran N., ALİKAŞİFOĞLU A., Gonc N., Ozon A., KANDEMİR N., Yordarn N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.21, sa.1, ss.63-72, 2008 (SCI-Expanded) identifier identifier

Effect of initial dose of L-Thyroxine on serum hormone levels in congenital hypothyroidism

Ozon A., Gumus P., ALİKAŞİFOĞLU A., Gonc N., KANDEMİR N.
HORMONE RESEARCH , cilt.70, ss.175-176, 2008 (SCI-Expanded) identifier

Is ACTH stimulation test essential for all cases with premature adrenarche?

Gonc N., Engiz O., ALİKAŞİFOĞLU A., Ozon A., BULUM AKBULUT B., KANDEMİR N.
HORMONE RESEARCH , cilt.70, ss.145, 2008 (SCI-Expanded) identifier

A clinical review of patients with 45 XO/46 XY genotype

ALİKAŞİFOĞLU A., DEMİRBİLEK H., Ozon A., Gonc N., Kandemir N.
HORMONE RESEARCH , cilt.70, ss.156, 2008 (SCI-Expanded) identifier

Hashimoto's thyroiditis in children and adolescents: A retrospective study on clinical, epidemiological and laboratory properties of the disease

DEMİRBİLEK H., KANDEMİR N., GÖNÇ E. N., Ozon A., ALİKAŞİFOĞLU A., Yordam N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.20, sa.11, ss.1199-1205, 2007 (SCI-Expanded) identifier identifier identifier

Central diabetes insipidus associated with Caroli syndrome

Cetinkaya S., Alikasifoglu A.
INDIAN JOURNAL OF PEDIATRICS , cilt.74, sa.4, ss.419-420, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Inappropriate use of potent topical glucocorticoids in infants

Ozon A., Cetinkaya S., Alikasifoglu A., Gonc E. N., Sen Y., Kandemir N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.20, sa.2, ss.219-225, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Use of bisphosphonates for resistant hypercalcemia in children with acute lymphoblastic leukemia: report of two cases and review of the literature

Andiran N., Alikasifoglu A., Kuepeli S., Yetgin S.
TURKISH JOURNAL OF PEDIATRICS , cilt.48, sa.3, ss.248-252, 2006 (SCI-Expanded) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Challenges During the Coronavirus Disease 2019 Pandemic: Diabetes Control and Psychosocial Issues in Children with Type 1 Diabetes Mellitus and Their Mothers

Emet D. C., Yeşil A. M., Çelik B., Şencan B., ÜNSAL Y., Gönç N., et al.
Turkish Archives of Pediatrics , cilt.58, sa.4, ss.418-424, 2023 (Scopus) identifier identifier

Psychosocial Impact of the COVID-19 Pandemic on Children with Congenital Adrenal Hyperplasia and Their Families

Çelik N. B., Ünsal Y., Emet D. C., Yeşil A. M., Şencan B., GÖNÇ E. N., et al.
Turkish Archives of Pediatrics , cilt.57, sa.6, ss.621-629, 2022 (Scopus) identifier identifier identifier

Adequacy of basal luteinizing hormone levels in the diagnosis of central precocious puberty

Vuralli D., GÖNÇ E. N., ÖZÖN Z. A., ALİKAŞİFOĞLU A.
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.55, sa.2, ss.131-138, 2020 (ESCI) Creative Commons License identifier identifier identifier

Monogenik diyabet

AKGÜN DOĞAN Ö., ÜTİNE G. E., ALİKAŞİFOĞLU A.
COCUK SAGLIGI VE HASTALIKLARI DERGISI , cilt.59, sa.3, ss.140-151, 2016 (Scopus)

An Adult Patient with Monosomy 18p Growth Hormone Deficiency and Selective IgA Deficiency

ZENGİN AKKUŞ P., çetinkaya a., ÇAĞDAŞ AYVAZ D. N., ALİKAŞİFOĞLU M., ALİKAŞİFOĞLU A., KANDEMİR N., et al.
Journal of Genetic Syndromes & Gene Therapy , cilt.7, sa.2, 2016 (Hakemli Dergi)

Pituitary hypoplasia and growth hormone deficiency in a woman with glycogen storage disease type Ia: A case report

DAĞDELEN S., Atmaca A., Alikasifoglu A., Erbas T.
Journal of Medical Case Reports , cilt.2, 2008 (Scopus) Creative Commons License identifier identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Kistik fibrozisli çocuklarda HbA1c ile solunum fonksiyonları ve günlük yaşam aktiviteleri arasındaki ilişkinin incelenmesi

KOCAAĞA E., İNAL İNCE D., ADEMHAN TURAL D., BOZDEMİR ÖZEL C., ÇALIK KÜTÜKCÜ E., VARDAR YAĞLI N., et al.
9. Ulusal Çocuk Solunum Yolu Hastalıkları ve Kistik Fibrozis Kongresi, Türkiye, 5 - 07 Mart 2020, ss.89

Oral Health and Halitosis of Status Type 1 Diabetic Children: A Descriptive Study

İŞCAN T. A., UZAMIŞ TEKÇİÇEK M., İLERİ KEÇELİ T., ALİKAŞİFOĞLU A., DOĞAN B.
EADPH Congress-Patient-centered care: multi-sectoral approaches to improving oral health., 12 - 14 Eylül 2019 Sürdürülebilir Kalkınma

Kistik Fibrozis Tanılı Hastalarda Glukoz Metabolizmasının Degerlendirilmesi

gözmen o., DOĞRU ERSÖZ D., ALİKAŞİFOĞLU A., Ademhan D., EMİRALİOĞLU N., YALÇIN E. E., et al.
Çocuk Göğüs Hastalıkları 4. Kongresi, Türkiye, 9 - 11 Ekim 2019

Spondyloocular syndrome: Presentation of two siblings diagnosed with the rare disease and the results of Pamidronate Therapy

VURALLI KARAOĞLAN D., ŞİMŞEK KİPER P. Ö., UTİNE G. E., ÜNSAL Y., ALİKAŞİFOĞLU A., KANDEMİR N.
The 58th Annual ESPE Meeting, VİYANA, Avusturya, 19 - 21 Eylül 2019, cilt.91, ss.387

Unusual Presentation of Autoimmune Polyglandular Syndrome Type 1 (Aps1)

VURALLI KARAOĞLAN D., TAN Ç., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ., DEMİR H., HIZARCIOĞLU GÜLŞEN H., et al.
58th Annual ESPE, Viyana, Avusturya, 19 - 21 Eylül 2019, cilt.91, ss.245-246 identifier

A Rare Cause of Hyperinsulinemic Hypoglycemia: Costello Syndrome

VURALLI KARAOĞLAN D., KOŞUKCU C., TAŞKIRAN Z. E., ŞİMŞEK KİPER P. Ö., UTİNE G. E., BODUROĞLU O. K., et al.
57th Annual ESPE European Society for Paediatric Endocrinology, Atina, Yunanistan, 27 - 29 Eylül 2018, cilt.90, ss.351-352

IGF1 Receptor Deletion is a Rare Cause of Prenatal Onset Short Stature.

GÖNÇ E. N., ÖZÖN Z. A., Kabaçam S., ŞİMŞEK KİPER P. Ö., ÜTİNE G. E., ALİKAŞİFOĞLU A., et al.
International Congress of the Growth Hormone Research IGF Societies, Sep 14 - 17, 2018, Seattle, Washington, United States of America., 14 - 17 Eylül 2018

Biotin May Lead To High Free Thyroxine Levels in Some Immunoassay Methods

PORTAKAL AKÇİN O., GÖNÜL G., GÖNÇ E. N., SİVRİ H. S., ALİKAŞİFOĞLU A., YİĞİT Ş., et al.
69th AACC ANNUAL SCIENTIFIC MEETING, SAN DIEGO, Amerika Birleşik Devletleri, 30 Temmuz - 03 Ağustos 2017, cilt.63

Hypercalcemia developing in three cases following discontinuation of denosumab treatment.

ÖZÖN Z. A., BÜYÜKYILMAZ G., ALİKAŞİFOĞLU A., GÖNÇ E. N., KURUCU N., AKYÜZ C.
10th International Meeting of Pediatric Endocrinolgy, 14 - 17 Eylül 2017

SOX9 gene dublication-related 46,XX ovotesticular disorder of sex development

ÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., BÜYÜKYILMAZ G., ŞİMŞEK KİPER P. Ö., et al.
10th International Meeting of Pediatric Endocrinolgy, 14 - 17 Eylül 2017

Sox9 gene duplication-related 46, XX ovotesticular disorder of sex development

ÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., BÜYÜKYILMAZ G., ŞİMŞEK KİPER P. Ö., et al.
10th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 14 - 17 Eylül 2017, cilt.88, ss.371

Duplication ina patient presenting with SRY negative 46XX disorders of sex development

ŞİMŞEK KİPER P. Ö., ÖZÖN Z. A., GÖNÇ E. N., ALİKAŞİFOĞLU A., ÜTİNE G. E., BODUROĞLU O. K., et al.
50th The European Society of Human Genetics, 27 - 29 Mayıs 2017

Kardeşi Tip 1 Diabetes Mellitus Tanısı ile İzlenen Sağlıklı Ergenlerin Yeme Tutumlarının Değerlendirilmesi

AKGÜL S., ALİKAŞİFOĞLU A., Sine Ö., Özon A., GÖNÇ E. N., DÜZÇEKER Y., et al.
21. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 26 - 30 Nisan 2017 Sürdürülebilir Kalkınma

Konjenital hipofiz sapı kesisine bağlı çoklu hipofiz hormon eksikliği ve hiperprolaktinemi: Nadir presentasyon galaktore

ALİKAŞİFOĞLU A., YAMAN B., GÖNÇ E. N., ÖZÖN Z. A., KARLI OĞUZ H. K., KANDEMİR N.
XXI. Ulusal Pediatrik Endokrinoloji veDiyabet Kongresi, Antalya, Türkiye, 26 - 30 Nisan 2017

SOX9 gen dublikasyonuna bağlı 46,XX ovotestiküler cinsel farklılaşma bozukluğu.

ÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., Büyükyılmaz G., ŞİMŞEK KİPER P. Ö., et al.
XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 26 - 30 Nisan 2017, ss.117

Erişkin boya erişen klasik konjenital adrenal hiperplazili olgularda hormon kontrolünün deksametazonla sağlanması.

GÖNÇ E. N., ÖZÖN Z. A., ALİKAŞİFOĞLU A., VURALLI KARAOĞLAN D., KANDEMİR N.
XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi., Antalya, Türkiye, 26 - 30 Nisan 2017, ss.76

Denosumab tedavisinin kesilmesini takiben üç olguda gelişen hiperkalsemi

ÖZÖN Z. A., BÜYÜKYILMAZ G., ALİKAŞİFOĞLU A., GÖNÇ E. N., KURUCU N., AKYÜZ C.
XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 26 - 30 Nisan 2017

SOX9 gen duplikasyonuna bağlı 46,XX ovotestiküler cinsel farklılaşma bozukluğu

ÖZÖN Z. A., ALİKAŞİFOĞLU A., GÖNÇ E. N., VURALLI KARAOĞLAN D., Büyükyılmaz G., ŞİMŞEK KİPER P. Ö., et al.
XXı.Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 26 - 30 Nisan 2017

Kardeşi tip 1 diyabetes mellitus tanısı ile izlenen sağlıklı ergenlerin yeme tutumlarının değerlendirilmesi

AKGUL S., ALİKAŞİFOĞLU A., ÖRS S., ÖZÖN Z. A., GÖNÇ E. N., YAS D., et al.
21. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 26 - 30 Nisan 2017 Sürdürülebilir Kalkınma

Septo-optik displazi (De Morsier Sendromu) ve çoklu hipofiz hormon eksikliği ile izlenen kız olguda puberte prekoks

GÖNÇ E. N., YAMAN B., ÖZÖN Z. A., ALİKAŞİFOĞLU A.
XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 26 - 30 Nisan 2017

Kardeşi Tip I DM ile izlenen sağlıklı ergenlerin yeme tutumunun değerlendirilmesi

AKGÜL S., ALİKAŞİFOĞLU A., YILMAZ S., ÖZÖN Z. A., GÖNÇ E. N., DÜZÇEKER Y., et al.
XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 26 - 30 Nisan 2017

Cinsiyet disforisi olan iki olgu sunumu

ÖZÖN Z. A., BÜYÜKYILMAZ G., ALİKAŞİFOĞLU A., AKGÜL S., ASLAN C., GÖNÇ E. N.
XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 26 - 30 Nisan 2017

Serum IGF1 and IGFBP3 levels in SMA patients

Yeşbek Kaymaz A., Köstel Bal S., Bora G., Özön Z. A., Alikaşifoğlu A., Topaloğlu H. A., et al.
21 st World Muscle Society, Granada, İspanya, 4 - 08 Ekim 2016

Serum IGF1 and IGFBP3 levels in SMA patients

Kaymaz A., Bal A., Bora-Tatar G., Ozon A., ALİKAŞİFOĞLU A., TOPALOĞLU H. A., et al.
21st International Congress of the World-Muscle-Society, Granada, Nikaragua, 4 - 08 Ekim 2016, cilt.26 identifier

Clinical and Molecular Analysis of 3M Syndrome Patients A Study From Turkey

ŞİMŞEK KİPER P. Ö., TAŞKIRAN Z. E., ÜTİNE G. E., ALİKAŞİFOĞLU A., KANDEMİR N., Cormier Daire V., et al.
28th International Congress of Pediatrics, 17 - 22 Ağustos 2016

IGF System Elements in SMA Patients

YEŞBEK KAYMAZ A., Köstel Bal S., BORA G., ÖZÖN Z. A., ALİKAŞİFOĞLU A., TOPALOĞLU H. A., et al.
20th Annual Spinal Muscular Atrophy Researcher Meeting, Anaheim, Amerika Birleşik Devletleri, 16 - 19 Haziran 2016

OBSL1 Mutations Represent The Major Gene Defect In A Group Of 3M Syndrome Patients A Study From Turkey

ŞİMŞEK KİPER P. Ö., Taşkıran E. Z., ARSLAN U., Koşukçu C., AKGÜN DOĞAN Ö., ÜTİNE G. E., et al.
European Society of Human Genetics Conference 2016, 21 - 24 Mayıs 2016

Dismorfik Bulguları ve Selektif IgA Eksikliği Tanısıyla İzlenen Monozomi 18p Olgusu

ZENGİN AKKUŞ P., ÇETİNKAYA A., ÇAĞDAŞ AYVAZ D. N., ALİKAŞİFOĞLU M., ALİKAŞİFOĞLU A., KANDEMİR N., et al.
2. Klinik İmmünoloji Kongresi, Antalya, Türkiye, 31 Mart - 03 Nisan 2016

3M Sendromlu Bir Grup Hastada Klinik Ve Moleküler Bulguların Analizi

ŞİMŞEK KİPER P. Ö., EKİM ZİHNİ T., ÜTİNE G. E., ALİKAŞİFOĞLU A., KANDEMİR N., VALERİE C. D., et al.
2. Ulusal Çocuk Genetik Sempozyumu, 22-24 Ekim 2015, Samsun, Türkiye, Türkiye, 22 - 24 Ekim 2015

Severe congenital hyperinsulinism in a neonate homozygous for two novel missense mutations in the KCNJ11 gene

ÖZÖN Z. A., ALİKAŞİFOĞLU A., SİAN e., ARAH f., GÖNÇ E. N., KANDEMİR N.
54th Annual Meeting of European Society for Paediatric Endocrinology (ESPE), 1 - 04 Ekim 2015

Long Term Effects of Bisphosphonate Treatment in a Case with Infantile Onset Severe form of Juvenile Paget s Disease

GÖNÇ E. N., ÖZÖN Z. A., GÖNÜL B., ALİKAŞİFOĞLU A., ŞİMŞEK KİPER P. Ö., KANDEMİR N.
54th Annual ESPE Meeting, October 1st-October 3rd, 2015, Barcelona, Spain, Abstract Book p340., 1 - 03 Ekim 2015

Clinical and Molecular Analysis of 3M Syndrome In A Group of Turkish Patients

ŞİMŞEK KİPER P. Ö., EKİM ZİHNİ T., ÜTİNE G. E., ALİKAŞİFOĞLU A., KANDEMİR N., VALERİE C. D., et al.
International Skeletal Dysplasia Society 12th Biennial Meeting, 29 Temmuz - 01 Ağustos 2015

Anorexia Nervosa ve Haşimoto Tiroiditi Beraberliği

AKGÜL S., Melis K., KANBUR N., ALİKAŞİFOĞLU A.
5. Ulusal Ergen Sağlığı Kongresi, Türkiye, 27 - 29 Kasım 2014

Metrikler

Yayın

126

Atıf (WoS)

408

H-İndeks (WoS)

11

Atıf (Scopus)

325

H-İndeks (Scopus)

11

Proje

11

Açık Erişim

18
BM Sürdürülebilir Kalkınma Amaçları