Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects.

The Journal of clinical endocrinology and metabolism, vol.106, no.10, 2021 (Journal Indexed in SCI Expanded) identifier identifier identifier

Severe Hypophosphatemic Rickets due to Tumor-Induced Osteomalasia

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.209, 2021 (Journal Indexed in SCI) identifier

Hyperinsulinemic hypoglycemia due to biallelic mutations in the DNAJC3 gene

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.107, 2021 (Journal Indexed in SCI) identifier

Is quail egg a potential endocrine disruptor?

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.364, 2021 (Journal Indexed in SCI) identifier

Endocrine disrupting chemicals and bone.

Best practice & research. Clinical endocrinology & metabolism, vol.35, 2021 (Journal Indexed in SCI) identifier identifier identifier

A rare cause of hypercalcemia: Congenital Lactase Deficiency

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.75, 2021 (Journal Indexed in SCI) identifier

46,XY DSD due to biallelic DHX37 gene mutations

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.393-394, 2021 (Journal Indexed in SCI) identifier

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.12, no.2, pp.150-159, 2020 (Journal Indexed in SCI) identifier identifier identifier

Clinical Significance of Hypophosphatasemia in Children

CALCIFIED TISSUE INTERNATIONAL, vol.106, no.6, pp.608-615, 2020 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Revisiting Classical 3 beta-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.105, no.4, 2020 (Journal Indexed in SCI) identifier identifier identifier

A rare cause of hypertension in childhood: Answers

Pediatric Nephrology, vol.35, no.1, pp.79-82, 2020 (Journal Indexed in SCI) identifier identifier identifier

A rare cause of hypertension in childhood: Questions

PEDIATRIC NEPHROLOGY, vol.35, no.1, pp.77-78, 2020 (Journal Indexed in SCI) identifier identifier identifier

Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study.

Diabetic medicine : a journal of the British Diabetic Association, vol.36, no.10, pp.1243-1250, 2019 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

A rare cause of hypophosphatemia: Raine Syndrome

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.384, 2019 (Journal Indexed in SCI) identifier

Evaluation of brain MRI lesions in 381 girls with central precocious puberty

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.329-330, 2019 (Journal Indexed in SCI) identifier

Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.214, 2019 (Journal Indexed in SCI) identifier

A Case Of Syndromic Hypopituitarism

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.589, 2019 (Journal Indexed in SCI) identifier

Liraglutide in children and adolescents with type 2 diabetes

New England Journal of Medicine, vol.381, no.7, pp.637-646, 2019 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease

Journal of Clinical Endocrinology and Metabolism, vol.104, no.8, pp.3049-3067, 2019 (Journal Indexed in SCI) identifier identifier identifier

Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, vol.18, no.2, pp.229-236, 2019 (Journal Indexed in SCI) identifier identifier identifier

Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.179, no.6, pp.908-914, 2019 (Journal Indexed in SCI) identifier identifier identifier

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

Journal of clinical research in pediatric endocrinology, vol.11, no.2, pp.149-156, 2019 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

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

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.10, no.4, pp.336-342, 2018 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

THE CO-EXISTENCE OF TWO RARE DISEASES: A CASE REPORT

PEDIATRIC NEPHROLOGY, vol.33, no.10, pp.1881, 2018 (Journal Indexed in SCI) identifier

The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience

Journal of clinical research in pediatric endocrinology, vol.10, no.2, pp.125-130, 2018 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

An Unusual Cause of Short Stature

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.184-185, 2018 (Journal Indexed in SCI) identifier

Delayed Diagnosis of a Patient with Antley-Bixler Syndrome

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.166-167, 2018 (Journal Indexed in SCI) identifier

Nationwide Hypophosphatemic Rickets Study

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.109-110, 2018 (Journal Indexed in SCI) identifier

Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.9, pp.58-68, 2017 (Journal Indexed in SCI) identifier identifier identifier

Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients.

Journal of pediatric and adolescent gynecology, vol.30, no.4, pp.449-455, 2017 (Journal Indexed in SCI Expanded) identifier identifier identifier

Heterotrimeric G proteins in the control of parathyroid hormone actions

JOURNAL OF MOLECULAR ENDOCRINOLOGY, vol.58, no.4, 2017 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Pycnodysostosis at otorhinolaryngology

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, vol.95, pp.91-96, 2017 (Journal Indexed in SCI) identifier identifier identifier

CLINICAL CHARACTERISTICS OF TURKISH CHILDREN AND ADOLESCENTS WITH TYPE 2 DIABETES

HORMONE RESEARCH IN PAEDIATRICS, vol.88, pp.282, 2017 (Journal Indexed in SCI) Sustainable Development identifier

Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect

JCRPE Journal of Clinical Research in Pediatric Endocrinology, vol.8, pp.14, 2016 (Journal Indexed in SCI Expanded) identifier

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.101, no.5, pp.1980-1988, 2016 (Journal Indexed in SCI) identifier identifier identifier

Reconsideration of Mid-Parental Height Calculation

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.451, 2016 (Journal Indexed in SCI) identifier

Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.175-176, 2016 (Journal Indexed in SCI) identifier

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.101, no.1, pp.283-291, 2016 (Journal Indexed in SCI) identifier identifier identifier

Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.167, 2016 (Journal Indexed in SCI) identifier

H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis.

Acta dermato-venereologica, vol.95, no.8, pp.1021-3, 2015 (Journal Indexed in SCI Expanded) identifier identifier

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.7, no.3, pp.183-191, 2015 (Journal Indexed in SCI) identifier identifier identifier

GNAS Spectrum of Disorders

CURRENT OSTEOPOROSIS REPORTS, vol.13, no.3, pp.146-158, 2015 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.7, no.2, pp.98-101, 2015 (Journal Indexed in SCI) identifier identifier identifier

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.7, no.1, pp.37-44, 2015 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.7, no.1, pp.27-36, 2015 (Journal Indexed in SCI) identifier

Prevalence of acne in primary school children and the relationship of acne with pubertal maturation

TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY, vol.48, no.4, pp.182-186, 2014 (Journal Indexed in SCI) identifier identifier

Sleep disordered breathing in pycnodysostosis patients

EUROPEAN RESPIRATORY JOURNAL, vol.44, 2014 (Journal Indexed in SCI) identifier

Current research on pycnodysostosis.

Intractable & rare diseases research, vol.3, no.3, pp.91-3, 2014 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia.

European journal of pediatrics, vol.172, no.6, pp.851-3, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

Maternal Thyroid Dysfunction and Neonatal Thyroid Problems

INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, vol.2013, 2013 (Journal Indexed in SCI) identifier identifier identifier

Loss of XL alpha s (extra-large alpha s) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, vol.109, no.17, pp.6638-6643, 2012 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy

EUROPEAN JOURNAL OF ENDOCRINOLOGY, vol.166, no.1, pp.43-48, 2012 (Journal Indexed in SCI) identifier identifier identifier

Content analysis of food advertising in Turkish television

JOURNAL OF PAEDIATRICS AND CHILD HEALTH, vol.46, pp.427-430, 2010 (Journal Indexed in SCI) identifier identifier identifier

Electrocardiographic findings and QT dispersion in children with chest pain

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, vol.44, no.2, pp.53-56, 2009 (Journal Indexed in SCI) identifier

Cushing's Syndrome Due to a Non-Adrenal Ectopic Adrenocorticotropin-Secreting Ewing's Sarcoma in a Child

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.22, no.4, pp.363-368, 2009 (Journal Indexed in SCI) identifier

Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor

Journal of Clinical Endocrinology and Metabolism, vol.94, no.10, pp.3633-3639, 2009 (Journal Indexed in SCI) identifier identifier identifier

Alopecia: Association with resistance to thyroid hormones

Journal of Pediatric Endocrinology and Metabolism, vol.22, no.11, pp.1075-1081, 2009 (Journal Indexed in SCI) identifier identifier identifier

Adult height in Turkish patients with Turner syndrome without growth hormone treatment.

The Turkish journal of pediatrics, vol.50, no.5, pp.415-7, 2008 (Journal Indexed in SCI Expanded) identifier identifier identifier

Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients.

Journal of pediatric endocrinology & metabolism : JPEM, vol.21, no.8, pp.745-51, 2008 (Journal Indexed in SCI Expanded) identifier identifier identifier

Significance of acanthosis nigricans in childhood obesity

JOURNAL OF PAEDIATRICS AND CHILD HEALTH, vol.44, no.6, pp.338-341, 2008 (Journal Indexed in SCI) Sustainable Development identifier

Alendronate treatment in children with osteogenesis imperfecta

Indian Pediatrics, vol.45, no.2, pp.105-109, 2008 (Journal Indexed in SCI Expanded) identifier identifier identifier

Familial thyroid dysgenesis: Which genes could be involved?

HORMONE RESEARCH, vol.70, pp.163, 2008 (Journal Indexed in SCI) identifier

Constitutional growth delay pattern of growth in velo-cardio-facial syndrome: longitudinal follow up and final height of two cases.

Journal of clinical research in pediatric endocrinology, vol.1, no.1, pp.43-8, 2008 (Journal Indexed in SCI Expanded) identifier identifier

The effect of the mode of delivery on neonatal thyroid function.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, vol.20, no.6, pp.473-6, 2007 (Journal Indexed in SCI Expanded) identifier identifier identifier

Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method

Tohoku Journal of Experimental Medicine, vol.211, no.3, pp.243-249, 2007 (Journal Indexed in SCI) identifier identifier identifier

A case of thyroid hormone resistance syndrome in a newborn

HORMONE RESEARCH, vol.68, pp.52, 2007 (Journal Indexed in SCI) identifier

Reference data for bone speed of sound measurement by quantitative ultrasound in healthy children

Archives of Osteoporosis, vol.1, pp.37-41, 2006 (Journal Indexed in SCI Expanded) identifier

Severe diabetic ketoacidosis: hyperventilation or relative hypoventilation

PEDIATRIC CRITICAL CARE MEDICINE, vol.7, no.3, pp.291, 2006 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Compliance with treatment and follow-up in a pediatric obesity clinic

HORMONE RESEARCH, vol.65, pp.86, 2006 (Journal Indexed in SCI) Sustainable Development identifier

Evaluation of patients with Graves' disease

HORMONE RESEARCH, vol.65, pp.41, 2006 (Journal Indexed in SCI) identifier

Factors related to childhood obesity

HORMONE RESEARCH, vol.65, pp.82, 2006 (Journal Indexed in SCI) Sustainable Development identifier

Pycnodysostosis: A rare cause of short stature

HORMONE RESEARCH, vol.65, pp.76, 2006 (Journal Indexed in SCI) identifier

A patient with hypopituitarism and isochromosome 18q mosaicism

HORMONE RESEARCH, vol.64, no.6, pp.261-265, 2005 (Journal Indexed in SCI) identifier identifier identifier

Addition of orlistat to conventional treatment in adolescents with severe obesity

EUROPEAN JOURNAL OF PEDIATRICS, vol.163, no.12, pp.738-741, 2004 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Increased QT dispersion in breath-holding spells

ACTA PAEDIATRICA, vol.93, no.6, pp.770-774, 2004 (Journal Indexed in SCI) identifier identifier identifier

Two patients with Kabuki syndrome presenting with endocrine problems

Journal of Pediatric Endocrinology and Metabolism, vol.14, no.2, pp.215-220, 2001 (Journal Indexed in SCI) identifier identifier identifier

Etiological analysis of epilepsy during the infancy.

EPILEPSIA, vol.40, pp.226, 1999 (Journal Indexed in SCI) identifier

Articles Published in Other Journals

PREFACE

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, vol.83, 2020 (Journal Indexed in ESCI) identifier

GUIDELINES ON THE DIAGNOSIS AND MANAGEMENT OF X-LINKED HYPOPHOSPHATEMIA

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, vol.83, 2020 (Journal Indexed in ESCI) identifier

Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours.

Pediatric obesity, vol.11, no.5, pp.383-8, 2016 (Refereed Journals of Other Institutions) Sustainable Development identifier identifier identifier

CLINICAL AND CEPHALOMETRIC ANALYSIS OF THREE CASES WITH PYCNODYSOSTOSIS: CASE REPORTS

JOURNAL OF ISTANBUL UNIVERSITY FACULTY OF DENTISTRY, vol.49, no.1, pp.51-55, 2015 (Journal Indexed in ESCI) identifier

Renal agenezisi olan bir Beckwith-Wiedemann Olgusu

Türk Nefroloji Diyaliz ve Transplantasyon Dergisi, vol.16, pp.196-197, 2007 (Other Refereed National Journals)

Echocardiographic diagnosis of aortopulmonary window in a 4-day-old baby

Marmara Medical Journal, vol.12, no.2, pp.98-100, 1999 (Refereed Journals of Other Institutions) identifier

Refereed Congress / Symposium Publications in Proceedings

DISORDER OF ADRENAL EXCESS AND ADRENAL MEDULLA

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, Cairo, Egypt, 23 February - 01 March 2018

İnsülin Degludek/Aspart ile Az Çoktur !

25. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 06 October 2021

Toplumumuzda Osteogenezis İmperfektada Genetik Nedenler ve Genotip Fenotip İlişkisi

XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Turkey, 06 October 2021

PARATİROİD HASTALIKLARI VE YÖNETİMİ

VI. Pediatrik Endokrinoloji İleri Kursu, 11 June 2021

Pediatrik hastalarda IDegAsp kullanımı ile ilgili esaslar nelerdir?

42. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, 20 May 2021

Congenital adrenal hyperplasia

ESPE Winter School Online, 27 February 2021

Hyperthyroidism

ESPE Winter School Online, 27 February 2021

Bone related-comorbidities in children and adults with genetic conditions

European Calcified Tissue Society 2020 Digital Congress, Marseille, France, 22 - 24 October 2020

Oturum başkanlığı

Çocukluk çağı Nefro-endokrin hastalıklar sempozyumu, İstanbul, Turkey, 2 - 03 October 2020

Clinical Characteristics of Turkish Children and Adolescents with Type 2 Diabetes

10th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2020, vol.88, pp.1-628 Sustainable Development

TİP 1 DM TANILI HASTALARDA SESSİZ ÇÖLYAK HASTALIĞI

7. MARMARA PEDiATRi KONGRESi, İstanbul, Turkey, 20 - 22 February 2020, pp.106 Creative Commons License

Büyümenin Değerlendirilmesi

BAŞKENT ÜNİVERSİTESİ İSTANBUL UYGULAMA VE ARAŞTIRMA MERKEZİ ÇOCUK SAĞLIĞI VE HASTALIKLARI ANA BİLİM DALI İSTANBUL TOPLANTISI Pediatride Güncel Yaklaşımlar II, İstanbul, Turkey, 08 February 2020

Hypocalcem a and Hypercalcem a in Children

1st Internat onal Rumi  Pediatric Congress (IRUPEC), 4 - 07 December 2019

Rare Causes of Osteogenesis Imperfecta are Commonin Consanguineous Pedigrees

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019

A Case Of Syndromic Hypopituitarism

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, 19 - 21 September 2019, vol.91, pp.1-682 identifier identifier identifier

A rare cause of hypophosphatemia: Raine Syndrome

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91

Genotype and Phenotype Characterization ofTurkish Patients with Vitamin D Dependent RicketsType IA

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91

First international consensus statement on diagnosis and management of pseudohypoparathyroidism and related disorders

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.623-624 identifier

Psödohipoparatiroidi Uzlaşı Raporu

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 17 - 21 April 2019

Pediatrik Tiroid Kanserlerine Yaklaşım

15. Türk Rinoloji Kongresi, 7.Ulusal Otoloji Nörootoloji Kongresi ve 3.Ulusal Baş Boyun Cerrahisi Kongresine, Turkey, 4 - 07 April 2019 Sustainable Development

Çocuklukta Osteogenesis İmperfekta Klinik Yaklaşım ve Tedavide İlkeler :

3.Ege Endokrin Hastalıklar ve Genetik Sempozyumu, Turkey, 7 - 09 March 2019

Disorders of sexual differentiation

Disorders of sexual differentiation, 22 - 28 February 2019

Introduction to molecular endocrinology

ESPE Winter School, 22 - 28 February 2019

Congenital Adrenal Hyperplasia

ESPE Winter School, 22 - 28 February 2019

Metabolic bone diseases in children, diagnosis related to oral and dental manifestations

International Association of Pediatric Dentistry Regional Meeting, 12 - 14 November 2018

Psödohipoparatiroidi tanı ve tedavisi

Pediatrik Endokrinoloji İleri Kursu, Turkey, 2 - 04 November 2018

Düşük renin düzeyi: endokrin hipertansiyon

Çocuk Endokrinolojisi Olgu Sunumları-9, İstanbul, Turkey, 19 - 20 October 2018

The co-existence of two rare diseases: a case report

51th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Antalya, Turkey, 3 - 06 October 2018

Nationwide Hypophosphatemic Rickets Study

57.th Annual Meeting of the European Society for Paediatric Endocrinology(ESPE), ATİNA, Greece, 27 - 29 September 2018

ESPE Bone and Growth Plate Working Group (BGP)- Case Presentation

57th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 27 - 29 September 2018 identifier

Relation of serum IGF-1 and IGFBP3 levels with acute exacerbation in cystic fibrosis

28th International Congress of the European-Respiratory-Society (ERS), Paris, France, 15 - 19 September 2018, vol.52 identifier

Persistent Mullerian duct syndrome: Rare But Important Aetiology of an Inguinal Hernia and Cryptorchidism in Boys

HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 27 - 29 September 2018, vol.90, pp.568

Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene

HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, Athens, Greece, 27 - 29 September 2018, vol.90, pp.597

An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency

HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 27 - 29 September 2018, vol.90, pp.514 Sustainable Development

Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Turkey, 18 - 22 April 2018

BOY KISALIĞINA GENEL YAKLAŞIM

İSKELETİN GENETİK HASTALIKLARI KURSU, Turkey, 18 April 2018

Düşük Alkali Fosfotaz Düzeyinin Önemi

40. Pediatri Günleri ve 19. Pediatri Hemşireliği Günleri, Turkey, 8 - 11 April 2018

CONGENITAL ADRENAL HYPERPLASIA

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 February - 01 March 2018

INTRODUCTION TO MOLECULAR ENDOCRINOLOGY

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 February - 01 March 2018

DISORDER OF SEXUEL DEVELOPMENT

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 February - 01 March 2018

17OH-PREGNENOLONE SEEMS A MAJOR DRIVE OF ANDROGEN EXCESS IN PATIENTS WITH 11ß-HYDROXYLASE DEFICIENCY

. 10th Individual Abstracts for International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017

SIMULTANEOUS PROFILING OF 17 STEROID HORMONES USING LIQUID CHROMATOGRAPHY TANDEM MASS SPECTROMETRY IN NEWBORN AND EARLY INFANCY.

10th Individual Abstracts for International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017

17OH-pregnenolone seems a major drive of androgen excess in patient with 11 beta hydroxylase deficiency

10th Joint Meeting of Paediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2017, vol.88, pp.54

Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency

American Association of Clinical Chemistry Congress, Washington, United States Of America, 30 July - 03 August 2017

Congenital Adreal Hyperplasia

European Society for Paediatric Endocrinology-Winter School, 10 - 16 February 2017

Disorders of adrenocortical excess and adrenal medulla

European Society for Paediatric Endocrinology Winter School, 10 - 16 February 2017

Introduction to molecular endocrinology

European Society for Paediatric Endocrinology Winter School, 10 - 16 February 2017

Disorders of sexual differentiation

European Society for Paediatric Endocrinology Winter School, 10 - 16 February 2017

Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta

55th Annual Metting of the ESPE Paris, 10 - 12 September 2016, vol.86, pp.167

Reconsideration of Mid Parental Height Calculation

55th Annual Meeting of the ESPE, 10 - 12 September 2016, vol.86, pp.451

Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes

55th Annual Meeting of the ESPE, Paris, 10 - 12 September 2016, vol.86, pp.175-176

Neonatal Hypocalcemia

55th Annual Meeting of the ESPE, Paris, 10 - 12 September 2016

Current Perspective on Pseudohypoparathyroidism New Classification

Current Trends in Pediatric Endocrinology-A PES Perspective, 13 - 14 May 2016

Late Breaking news

Current Trends in Pediatric Endocrinology-A PES perspective, 13 - 14 May 2016

Disorders of SExual Differentiation

ESPE Winter School, 18 - 24 March 2016

CAH Congenital Adrenal Hyperplasia

ESPE Winter School, 18 - 24 March 2016

Introduction to Molecular Endocrinology

ESPE Winter School, 18 - 24 March 2016

HPP Genel Değerlendirme

HİPOFOSFATAZYA DANIŞMA KURULU TOPLANTISI, Turkey, 16 December 2015

HİPOTİROİDİ VE TİROTOKSİKOZUN YENİDOĞAN ÜZERİNE ETKİSİ

GEBELİK VE TİROİD SEMPOZYUMU, Turkey, 12 December 2015

Diyabet ile yaşam

Diyabet ile Yaşam- Cerrahpaşa, Turkey, 13 November 2015 Sustainable Development

Growth Hormone Deficiency and Treatment

59th Turkish National Pediatric Congress joint with the 3rd Italian-Turkish-Iranian Pediatric Congress, 4 November - 08 February 2015

Piknodisostozis Otorinolaringolojik bulgular

37. TÜRK ULUSAL KULAK BURUN BOĞAZ VE BAŞ BOYUN CERRAHİSİ KONGRESİ, Turkey, 28 October - 01 November 2015

Periferal Puberte Prekokslu 129 Çocukta Etiyolojik Dağılım Ve Klinik Özellikler

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 22 - 24 October 2015

Otozomal Resesif Osteogenezis İmperfekta Populasyonumuzdaki Sıklığı Ve Genetik Nedenleri

19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Turkey, 22 - 24 October 2015

Nonklasik Konjenital Adrenal Hiperplazi Hastalarının Genotip Ve Fenotip Özellikleri

19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Turkey, 22 - 24 October 2015

Merkezi Yenidogan Tarama Programi ile Tani Almis Konjenital Hipotiroidili Vakalarimizin İzlemi

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 22 - 24 October 2015

YILLIK

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 22 - 24 October 2015

Temel genetik kavramlar ve kalıtım şekilleri

1. Pediatrik Endokrinolojiye Giriş Kursu, Turkey, 21 - 22 October 2015

Factors Effecting Response to Growth HormoneTreatment in Children with Turner Syndrome

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015

Central or Primary Hypothyroidism How toDifferentiate in Patients with Low T4 but MildlyElevated TSH Levels

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 1 - 03 October 2015

Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia Molecular and Clinical Characterisation of a Nationwide Cohort

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015

Hereditary Vitamin D Resistant Rickets Report of Four Cases with Successful Use of Intermittent Intravenous Calcium Via Peripheral Route

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015

The Diagnostic Treatment and Follow Up Features of Childhood Thyroid Malignancies A Preliminary Report

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 1 - 03 October 2015

Evaluating First Year Response and Final Height toGrowth Hormone Treatment in Growth HormoneDeficiency Based on Peak GH Levels on Testing

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015

Aetiological Spectrum and Clinical Characteristics of 129 Children with Gonadotropin Independent Precocious Puberty A Nationwide Cohort Study

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015

Friedreich s Ataxia Presenting with Diabetes Mellitusin an Adolescent

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 1 - 03 October 2015 Sustainable Development

Dysosteosclerosis from a unique mutation in SLC29A3

7th International Conference on Children's Bone Health, 27 - 30 June 2015

ANTLEY BİXLER SENDROMLU BİR OLGUMUZ

Cocuk Endokrinoloji Dernegi 7.Olgu Sunumlari Toplantisi, İzmir, Turkey, 18 - 20 May 2015

Current Practice in Diagnosis and Treatment of GH Deficiency in Childhood A Survey from Turkey

54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 1 - 03 October 2015

GEÇ ÇOCUKLUK ERKEN ERGENLİK

KANUNİ SULTAN SÜLEYMAN GÜNLERİ, Turkey, 20 - 21 February 2015

Dysosteosclerosis: Evidence for Genetic Heterogeneity

Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, Texas, United States Of America, 12 - 15 September 2014, vol.29 identifier

Subclinical PTH resistance in a patient with a novel heterozygous GNAS mutation: G alpha s haploinsufficiency as a plausible cause.

Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, Maryland, United States Of America, 4 - 07 October 2013, vol.28 identifier

Identification of 18q12 2 q21 1 Deletion A Case Report

9th National Medical Genetics Congress of Turkish Medical Society with international Participation., 1 - 05 December 2010

Maternal Thyroid Dysfunction and Neonatal Problems

2nd Interanational Congress of UENPS, İstanbul, Turkey, 15 - 17 November 2010

Identification of novel dentin matrix protein-1 (DMP1) mutations in two unrelated kindreds with autosomal recessive hypophosphatemia

29th Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, Hawaii, United States Of America, 16 - 19 September 2007, vol.22 identifier

Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.125-126 identifier

Books & Book Chapters

Hipofosfatemik Raşitizm

in: Çocuk Endokrinolojisi Ve Diyabet, Darendeliler Feyza, Zehra Aycan, Cengiz Kara, Samim Özen, Erdal Eren, Editor, İstanbul Tıp Kitabevi, İstanbul, pp.1874-1900, 2021

Hipokalsemi

in: Çocuk Endokrinolojisi ve Diyabet, Darendeliler Feyza, Zehra Aycan, Cengiz Kara, Samim Özen, Erdal Eren, Editor, İstanbul Tıp Kitabevi, İstanbul, pp.1748-1773, 2021

İlk beş yaş kronik endokrin problemi olan çocuk izlemi

in: İlk Beş Yaş Çocuk Sağlığı İzlemi, Gökçay G,Beyazova U, Editor, Nobel Tıp Kitapevi, İstanbul, pp.82-86, 2017

Hipofosfatemik rikets ve diğer herediter rikets türleri

in: Yurdakök Pediyatri , Yurdakök M, Editor, Güneş Kitabevi, Ankara, pp.4055-4072, 2017

GNAS Complex Locus

in: Encyclopedia of Signaling Molecules, Sangdun Choi, Editor, Springer New York, New-York, pp.1-13, 2017

Jinekomasti

in: Adolesan Sağlığı ‘Koruyucu hekimlik ve erken tanı’, Apaydın Kaya C, Editor, Nobel Tıp Kitapevi, İstanbul, pp.503-508, 2015

Obezitenin değerlendirilmesi ve yönetimi

in: Adolesan Sağlığı ‘Koruyucu hekimlik ve erken tanı’, Apaydın Kaya C, Editor, Nobel Tıp Kitapevi, İstanbul, pp.467-481, 2015

İskelet Displazilerinde Peroperatif yaklaşım

in: Çocuklarda Acil Endokrin Hastalıklar, Kurtoglu S, Editor, Nobel Tıp Kitapevi, Ankara, pp.483-496, 2013

İskelet Displazileri

in: Yenidoğan Dönemi Endokrin Hastalıkları., Kurtoglu S, Editor, Nobel Yayın Dağıtım, Ankara, pp.300-315, 2011

ÇocChildhood diabetic ketoacidosis treatmentuklarda diyabetik ketoasidoz ve tedavisi

in: Pediatrik yogun bakim: Prensipler ve uygulamalar, Karabocuoglu ve T.F. Koroglu, Editor, İstanbul Medikal Yayıncılık, İstanbul, pp.629-638, 2008

Neonatal Hipoglisemi

in: Basic Rules and Emergency Care in Neonatalogy- Neonatal Hypoglycemia, M. Tuncer ve E. Ozek, Editor, Güneş Kitabevi, İstanbul, pp.373-383, 2007

Serum IGF-I and IGFBP-3 levels-Their role in clinical evaluation of he diseases

in: Çocuk ve Adolesanda Endokrin Testler, , N. Yordam,A. Alikasifoglu ve A. Bideci, Editor, Güneş Kitabevi, Ankara, pp.23-48, 2006

Neonatal thyroid emergencies

in: Basic Rules and Emergency Care in Neonatology, M. Tuncer ve E. Ozek, Editor, Güneş Kitabevi, İstanbul, pp.359-379, 2006

Expert Reports