Prof. Dr. NURGÜN KANDEMİR

Metrikler

Yayın

Yayın (WoS)

Yayın (Scopus)

Atıf (WoS)

741

H-İndeks (WoS)

Atıf (Scopus)

373

H-İndeks (Scopus)

Atıf (Scholar)

H-İndeks (Scholar)

Atıf (Diğer Toplam)

Proje

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

Eğitim Bilgileri

1991 - 1994

Tıpta Yandal Uzmanlık

Hacettepe Üniversitesi, Tıp Fakültesi, Pediatrik Endokrin, Türkiye

1985 - 1991

Tıpta Uzmanlık

Hacettepe Üniversitesi, Tıp Fakültesi, Çocuk Sağlığı Ve Hastalıkları, Türkiye

1977 - 1983

Lisans

Hacettepe Üniversitesi, Tıp Fakültesi, Türkiye

Araştırma Alanları

Tıp

Sağlık Bilimleri

Dahili Tıp Bilimleri

Çocuk Sağlığı ve Hastalıkları

Pediatrik Endokrinoloji ve Metabolizma

Akademik Faaliyetlere Dayalı Araştırma Alanları

Avesis Araştırma Alanları

WoS Araştırma Alanları

Scopus Araştırma Alanları

Akademik Ünvanlar / Görevler

2002 - Devam Ediyor

Prof. Dr.

Hacettepe Üniversitesi, Hacettepe Tıp Fakültesı

2002 - 2016

Prof. Dr.

Hacettepe Üniversitesi, Tıp Fakültesi

Makaleler

2024

1. Long-term Growth Hormone Therapy in a Patient with IGF1R Deletion Accompanied by Delayed Puberty and Central Hypothyroidism

ÇELİK ERTAŞ N. B., Losekoot M., Isik E., GÖNÇ E. N., ALİKAŞİFOĞLU A., KANDEMİR N., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , sa.4, ss.481-488, 2024 (SCI-Expanded, Scopus, TRDizin)

2024

2. Exploring metabolic alterations in PYCR2 deficiency: Unveiling pathways and clinical presentations of hypomyelinating leukodystrophy 10

Gurbuz B. B., GÜLBAKAN B., ÖZGÜL R. K., YALNIZOĞLU D., Yilmaz D. Y., GÖÇMEN R., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.194, sa.9, 2024 (SCI-Expanded, Scopus)

2024

3. Epidemiology of type 1 diabetes mellitus in children and adolescents: A 50-year, single-center experience

KANDEMİR N., VURALLI KARAOĞLAN D., Ozon A., Gonc N., ARDIÇLI D., Jalilova L., et al.

JOURNAL OF DIABETES , cilt.16, sa.5, 2024 (SCI-Expanded, Scopus)

2023

4. Genetic findings in short Turkish children born to consanguineous parents

Joustra S., Isik E., Wit J. M., ÇATLI G., ANIK A., HALİLOĞLU B., et al.

HORMONE RESEARCH IN PAEDIATRICS , ss.89-90, 2023 (SCI-Expanded, Scopus)

2022

5. Body composition in sexual precocity

GÖNÇ E. N., KANDEMİR N.

CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY , cilt.29, sa.1, ss.78-83, 2022 (SCI-Expanded, Scopus)

2022

6. 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, Scopus)

2021

7. 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, Scopus)

2021

8. 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, Scopus)

2021

9. 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, Scopus)

2021

10. 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, Scopus, TRDizin)

2021

11. 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, Scopus)

2021

12. 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, Scopus)

2021

13. 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, Scopus)

2021

14. 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, Scopus)

2021

15. Urinary bisphenol A levels in prepubertal children with exogenous obesity according to presence of metabolic syndrome

Aktag E., YURDAKÖK K., YALÇIN S. S., KANDEMİR N.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.34, sa.4, ss.495-502, 2021 (SCI-Expanded, Scopus)

2020

16. 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, Scopus)

2020

17. 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, Scopus, TRDizin)

2020

18. 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, Scopus)

2020

19. 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, Scopus, TRDizin)

2020

20. 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, Scopus)

2020

21. 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, Scopus)

2020

22. What is the evidence for beneficial effects of growth hormone treatment beyond height in short children born small for gestational age? A review of published literature

Dunger D., Darendeliler F., KANDEMİR N., Harris M., Rabbani A., Kappelgaard A.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.33, sa.1, ss.53-70, 2020 (SCI-Expanded, Scopus)

2019

23. 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, Scopus)

2019

24. 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, Scopus)

2019

25. 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, Scopus)

2019

26. 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, Scopus)

2019

27. 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, Scopus)

2018

28. 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, Scopus)

2018

29. 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, Scopus)

2018

30. 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, Scopus)

2017

31. 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, Scopus, TRDizin)

2017

32. Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

Bertko E., Klammt J., Dusatkova P., Bahceci M., Gonc N., ten Have L., et al.

JOURNAL OF HUMAN GENETICS , cilt.62, sa.8, ss.755-762, 2017 (SCI-Expanded, Scopus)

2017

33. 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, Scopus)

2017

34. 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, Scopus)

2017

35. 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, Scopus, TRDizin)

2017

36. 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, Scopus)

2017

37. 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, Scopus)

2017

38. DIFFERENTIAL EFFECTS OF LOW-WEIGHT, AMENORRHEA AND EXERCISE ON BONE MICROARCHITECTURE AND STRENGTH ESTIMATES AT WEIGHT BEARING AND NON-WEIGHT BEARING SITES IN ADOLESCENT GIRLS AND YOUNG ADULTS

KANDEMİR N., Reyes K. J. C., Singhal V., Slattery M., Ackerman K., Tulsiani S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.19-20, 2017 (SCI-Expanded, Scopus)

2017

39. FRACTURE PREVALENCE IN RELATION TO LOW WEIGHT PARAMETERS AND MENSTRUAL STATUS IN ADOLESCENT GIRLS WITH ANOREXIA NERVOSA

KANDEMİR N., Becker K. R., Slattery M., Tulsiani S., Singhal V., Faje A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.444-445, 2017 (SCI-Expanded, Scopus)

2016

40. Surgical and clinical strategies in the management of thyroid medullary carcinoma in children with and without ret protooncogene mutations

Boybeyi-Turer O., Vuralli D., KARNAK İ., Gonc N., Yalcin E. S., ORHAN D., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.4, ss.436-441, 2016 (SCI-Expanded, Scopus, TRDizin)

2016

41. 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, Scopus, TRDizin)

2016

42. 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, Scopus)

2016

43. 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)

2015

44. 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, Scopus, TRDizin)

2015

45. Evidence of hypothalamic-pituitary-adrenal axis suppression during moderate-to-high-dose inhaled corticosteroid use

CAVKAYTAR O., VURALLİ D., Yilmaz E. A., Buyuktiryaki B., Soyer O., ŞAHİNER Ü. M., et al.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.174, sa.11, ss.1421-1431, 2015 (SCI-Expanded, Scopus)

2015

46. 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, Scopus)

2015

47. 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, Scopus, TRDizin)

2015

48. 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, Scopus)

2015

49. 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, Scopus)

2015

50. 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, Scopus)

2014

51. A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc

ÇAĞDAŞ AYVAZ D. N., YILMAZ M., KANDEMİR N., Tezcan I., Etzioni A., Sanal O.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.34, sa.8, ss.1009-1014, 2014 (SCI-Expanded, Scopus)

2014

52. 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, Scopus)

2014

53. 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, Scopus)

2013

54. 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, Scopus)

2013

55. An unexpected diagnosis in children with male phenotype and bilateral nonpalpable gonad: congenital adrenal hyperplasia with female genotype

Kirli E. A., KARNAK İ., ÇİFTÇİ A. Ö., KANDEMİR N., TANYEL F. C., Senocak M. E.

PEDIATRIC SURGERY INTERNATIONAL , cilt.29, sa.7, ss.719-724, 2013 (SCI-Expanded, Scopus)

2013

56. 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, Scopus)

2012

57. 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, Scopus)

2012

58. 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, Scopus)

2012

59. 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, Scopus)

2012

60. The role of the resistive index in Hashimoto's thyroiditis: a Sonographic pilot study in children

Sarikaya B., DEMİRBİLEK H., AKATA D., KANDEMİR N.

CLINICS , cilt.67, sa.11, ss.1253-1257, 2012 (SCI-Expanded, Scopus)

2012

61. 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, Scopus)

2012

62. 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, Scopus)

2011

63. 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, Scopus)

2011

64. 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, Scopus)

2011

65. 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, Scopus)

2011

66. 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, Scopus)

2010

67. Anemia and Neutropenic Fever with High Dose Diazoxide Treatment in a Case with Hyperinsulinism Due to Munchausen by Proxy

Ozon A., DEMİRBİLEK H., ERTUĞRUL A., ÜNAL S., GÜMRÜK F., KANDEMİR N.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.23, sa.7, ss.719-723, 2010 (SCI-Expanded, Scopus)

2009

68. 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, Scopus)

2009

69. 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, Scopus)

2009

70. 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)

2008

71. 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, Scopus)

2008

72. 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, Scopus)

2008

73. 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)

2008

74. 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, Scopus)

2008

75. 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)

2008

76. The effect of glucocorticoid replacement therapy and androgen levels on bone mineral density in children and adolescents with congenital adrenal hyperplasia

Unal S., KANDEMİR N.

HORMONE RESEARCH , cilt.70, ss.141, 2008 (SCI-Expanded)

2007

77. 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, Scopus)

2007

78. Thyroid involvement in Langerhans cell histiocytosis: a report of two cases and review of the literature

Yagci B., Kandemir N., Yazici N., Yalcin B., Varan A., Akyuz C., et al.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.166, sa.9, ss.901-904, 2007 (SCI-Expanded, Scopus)

2007

79. Long-term effects of growth hormone (GH) on bone mineral status and bone turnover markers in patients with isolated GH deficiency and multiple pituitary hormone deficiency

Gonc E. N., Kandemir N.

CLINICAL ENDOCRINOLOGY , cilt.66, sa.5, ss.672-677, 2007 (SCI-Expanded, Scopus)

2007

80. 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, Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler

2019

1. 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, (Özet Bildiri)

2018

2. 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, (Tam Metin Bildiri)

2017

3. 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, (Özet Bildiri)

2017

4. 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, (Özet Bildiri)

2016

5. 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, (Tam Metin Bildiri)

2016

6. 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, (Tam Metin Bildiri)

2016

7. 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, (Özet Bildiri)

2015

8. 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

2015

9. 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

2015

10. 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, (Tam Metin Bildiri)

2015

11. 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, (Tam Metin Bildiri)

Desteklenen Projeler

2015 - 2017

Anoreksiya Nervozanın pik kemik kitlesine etkisi

Yükseköğretim Kurumları Destekli Proje , BAP Araştırma Projesi

KANDEMİR N. (Yürütücü), MİSRA M.

2015 - 2015