Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.12, ss.150-159, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Clinical Significance of Hypophosphatasemia in Children

CALCIFIED TISSUE INTERNATIONAL, cilt.106, ss.608-615, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, cilt.105, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Restoration of Height after 11 Years of Letrozole Treatment in 11β-Hydroxylase Deficiency

Hormone Research in Paediatrics, cilt.92, ss.203-208, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A rare cause of hypertension in childhood: Answers

Pediatric Nephrology, cilt.35, ss.79-82, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A rare cause of hypertension in childhood: Questions

PEDIATRIC NEPHROLOGY, cilt.35, ss.77-78, 2020 (SCI İndekslerine Giren Dergi) 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, cilt.36, ss.1243-1250, 2019 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Simplifying the interpretation of steroid metabolome data by a machine-learning approach

HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.128, 2019 (SCI İndekslerine Giren Dergi) identifier

A rare cause of hypophosphatemia: Raine Syndrome

HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.384, 2019 (SCI İndekslerine Giren Dergi) identifier

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

HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.329-330, 2019 (SCI İndekslerine Giren Dergi) identifier

Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.214, 2019 (SCI İndekslerine Giren Dergi) identifier

A Case Of Syndromic Hypopituitarism

HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.589, 2019 (SCI İndekslerine Giren Dergi) identifier

Liraglutide in children and adolescents with type 2 diabetes

New England Journal of Medicine, cilt.381, ss.637-646, 2019 (SCI İndekslerine Giren Dergi) 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, cilt.104, ss.3049-3067, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

American Journal of Medical Genetics, Part A, cilt.179, ss.908-914, 2019 (SCI İndekslerine Giren Dergi) 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, cilt.18, ss.229-236, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

Journal of clinical research in pediatric endocrinology, cilt.11, ss.149-156, 2019 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans

EUROPEAN JOURNAL OF ENDOCRINOLOGY, cilt.180, ss.291-309, 2019 (SCI İndekslerine Giren Dergi) 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, cilt.10, ss.336-342, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

PEDIATRIC NEPHROLOGY, cilt.33, ss.1881, 2018 (SCI İndekslerine Giren Dergi) identifier

Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency

Human Molecular Genetics, cilt.27, ss.1913-1926, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

The distribution of different types of diabetes in childhood: A single center experience

JCRPE Journal of Clinical Research in Pediatric Endocrinology, cilt.10, ss.125-130, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

An Unusual Cause of Short Stature

HORMONE RESEARCH IN PAEDIATRICS, cilt.90, ss.184-185, 2018 (SCI İndekslerine Giren Dergi) identifier

Nationwide Hypophosphatemic Rickets Study

HORMONE RESEARCH IN PAEDIATRICS, cilt.90, ss.109-110, 2018 (SCI İndekslerine Giren Dergi) identifier

Delayed Diagnosis of a Patient with Antley-Bixler Syndrome

HORMONE RESEARCH IN PAEDIATRICS, cilt.90, ss.166-167, 2018 (SCI İndekslerine Giren Dergi) identifier

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

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.9, ss.58-68, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Heterotrimeric G proteins in the control of parathyroid hormone actions

JOURNAL OF MOLECULAR ENDOCRINOLOGY, cilt.58, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Pycnodysostosis at otorhinolaryngology

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, cilt.95, ss.91-96, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

HORMONE RESEARCH IN PAEDIATRICS, cilt.88, ss.54, 2017 (SCI İndekslerine Giren Dergi) identifier

CLINICAL CHARACTERISTICS OF TURKISH CHILDREN AND ADOLESCENTS WITH TYPE 2 DIABETES

HORMONE RESEARCH IN PAEDIATRICS, cilt.88, ss.282, 2017 (SCI İndekslerine Giren Dergi) 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, cilt.8, ss.14, 2016 (SCI Expanded İndekslerine Giren Dergi) identifier

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

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, cilt.101, ss.1980-1988, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Reconsideration of Mid-Parental Height Calculation

HORMONE RESEARCH IN PAEDIATRICS, cilt.86, ss.451, 2016 (SCI İndekslerine Giren Dergi) identifier

Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta

HORMONE RESEARCH IN PAEDIATRICS, cilt.86, ss.167, 2016 (SCI İndekslerine Giren Dergi) identifier

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

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, cilt.101, ss.283-291, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

HORMONE RESEARCH IN PAEDIATRICS, cilt.86, ss.175-176, 2016 (SCI İndekslerine Giren Dergi) identifier

Etiologic Distribution and Characteristics of Patients with Short Stature in a Pediatric Endocrinology Clinic

HORMONE RESEARCH IN PAEDIATRICS, cilt.86, ss.457-458, 2016 (SCI İndekslerine Giren Dergi) identifier

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

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.7, ss.183-191, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

GNAS Spectrum of Disorders

CURRENT OSTEOPOROSIS REPORTS, cilt.13, ss.146-158, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.7, ss.98-101, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.7, ss.27-36, 2015 (SCI İndekslerine Giren Dergi) identifier

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

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.7, ss.37-44, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

H Syndrome: A Multifaceted Histiocytic Disorder with Hyperpigmentation and Hypertriehosis

ACTA DERMATO-VENEREOLOGICA, cilt.95, ss.1021-1023, 2015 (SCI İndekslerine Giren Dergi) identifier

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

TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY, cilt.48, ss.182-186, 2014 (SCI İndekslerine Giren Dergi) identifier identifier

Sleep disordered breathing in children with endocrinological problems

EUROPEAN RESPIRATORY JOURNAL, cilt.44, 2014 (SCI İndekslerine Giren Dergi) identifier

Sleep disordered breathing in pycnodysostosis patients

EUROPEAN RESPIRATORY JOURNAL, cilt.44, 2014 (SCI İndekslerine Giren Dergi) identifier

Current research on pycnodysostosis.

Intractable & rare diseases research, cilt.3, ss.91-3, 2014 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License identifier identifier

Evaluation of bone metabolism in patients receiving home ventilation

EUROPEAN RESPIRATORY JOURNAL, cilt.42, 2013 (SCI İndekslerine Giren Dergi) identifier

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

EUROPEAN JOURNAL OF PEDIATRICS, cilt.172, ss.851-853, 2013 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Maternal Thyroid Dysfunction and Neonatal Thyroid Problems

INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2013 (SCI İndekslerine Giren Dergi) 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, cilt.109, ss.6638-6643, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

EUROPEAN JOURNAL OF ENDOCRINOLOGY, cilt.166, ss.43-48, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z-scores in Different Types of Rickets

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.3, ss.7-11, 2011 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Cognitive and psychosocial development in children with familial hypomagnesaemia

MAGNESIUM RESEARCH, cilt.24, ss.7-12, 2011 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Content analysis of food advertising in Turkish television

JOURNAL OF PAEDIATRICS AND CHILD HEALTH, cilt.46, ss.427-430, 2010 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Electrocardiographic findings and QT dispersion in children with chest pain

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.44, ss.53-56, 2009 (SCI İndekslerine Giren Dergi) identifier

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

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.22, ss.363-368, 2009 (SCI İndekslerine Giren Dergi) identifier

Cushing's syndrome due to a non-adrenal ectopic adrenocorticotropin- secreting ewing's sarcoma in a child

Journal of Pediatric Endocrinology and Metabolism, cilt.22, ss.363-368, 2009 (SCI İndekslerine Giren Dergi) identifier identifier 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, cilt.94, ss.3633-3639, 2009 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Alopecia: Association with resistance to thyroid hormones

Journal of Pediatric Endocrinology and Metabolism, cilt.22, ss.1075-1081, 2009 (SCI İndekslerine Giren Dergi) identifier identifier identifier

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

TURKISH JOURNAL OF PEDIATRICS, cilt.50, ss.415-417, 2008 (SCI İndekslerine Giren Dergi) identifier

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

The Turkish journal of pediatrics, cilt.50, ss.415-7, 2008 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.21, ss.745-51, 2008 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Significance of acanthosis nigricans in childhood obesity

JOURNAL OF PAEDIATRICS AND CHILD HEALTH, cilt.44, ss.338-341, 2008 (SCI İndekslerine Giren Dergi) identifier

Alendronate treatment in children with osteogenesis imperfecta

INDIAN PEDIATRICS, cilt.45, ss.105-109, 2008 (SCI İndekslerine Giren Dergi) identifier identifier 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, cilt.1, ss.43-8, 2008 (SCI Expanded İndekslerine Giren Dergi) identifier identifier

Familial thyroid dysgenesis: Which genes could be involved?

HORMONE RESEARCH, cilt.70, ss.163, 2008 (SCI İndekslerine Giren Dergi) identifier

Genetic testing of Turkish patients with pseudohypoparathyroidism type Ib

HORMONE RESEARCH, cilt.70, ss.50, 2008 (SCI İndekslerine Giren Dergi) identifier

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

Tohoku Journal of Experimental Medicine, cilt.211, ss.243-249, 2007 (SCI İndekslerine Giren Dergi) identifier identifier identifier

The effect of the mode of delivery on neonatal thyroid function

JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, cilt.20, ss.473-476, 2007 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A case of thyroid hormone resistance syndrome in a newborn

HORMONE RESEARCH, cilt.68, ss.52, 2007 (SCI İndekslerine Giren Dergi) identifier

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

Archives of Osteoporosis, cilt.1, ss.37-41, 2006 (SCI Expanded İndekslerine Giren Dergi) identifier

Severe diabetic ketoacidosis: hyperventilation or relative hypoventilation

PEDIATRIC CRITICAL CARE MEDICINE, cilt.7, ss.291, 2006 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Factors associated with obesity in children with hypothalamo-pituitary tumors

HORMONE RESEARCH, cilt.65, ss.83, 2006 (SCI İndekslerine Giren Dergi) identifier

Evaluation of patients with Graves' disease

HORMONE RESEARCH, cilt.65, ss.41, 2006 (SCI İndekslerine Giren Dergi) identifier

Factors related to childhood obesity

HORMONE RESEARCH, cilt.65, ss.82, 2006 (SCI İndekslerine Giren Dergi) identifier

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

HORMONE RESEARCH, cilt.65, ss.86, 2006 (SCI İndekslerine Giren Dergi) identifier

Pycnodysostosis: A rare cause of short stature

HORMONE RESEARCH, cilt.65, ss.76, 2006 (SCI İndekslerine Giren Dergi) identifier

A patient with hypopituitarism and isochromosome 18q mosaicism

HORMONE RESEARCH, cilt.64, ss.261-265, 2005 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Addition of orlistat to conventional treatment in adolescents with severe obesity

EUROPEAN JOURNAL OF PEDIATRICS, cilt.163, ss.738-741, 2004 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Increased QT dispersion in breath-holding spells

ACTA PAEDIATRICA, cilt.93, ss.770-774, 2004 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Two patients with Kabuki syndrome presenting with endocrine problems

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.14, ss.215-220, 2001 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Two patients with Kabuki syndrome presenting with endocrine problems

Journal of Pediatric Endocrinology and Metabolism, cilt.14, ss.215-220, 2001 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A case of glycogen storage disease type II with double aortic arch

ACTA PAEDIATRICA, cilt.89, ss.884-886, 2000 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Etiological analysis of epilepsy during the infancy.

EPILEPSIA, cilt.40, ss.226, 1999 (SCI İndekslerine Giren Dergi) identifier

Diğer Dergilerde Yayınlanan Makaleler

GUIDELINES ON THE DIAGNOSIS AND MANAGEMENT OF X-LINKED HYPOPHOSPHATEMIA

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.83, 2020 (ESCI İndekslerine Giren Dergi) identifier

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

JOURNAL OF ISTANBUL UNIVERSITY FACULTY OF DENTISTRY, cilt.49, ss.51-55, 2015 (ESCI İndekslerine Giren Dergi) identifier

Renal agenezisi olan bir Beckwith-Wiedemann Olgusu

Türk Nefroloji Diyaliz ve Transplantasyon Dergisi, cilt.16, ss.196-197, 2007 (Diğer Kurumların Hakemli Dergileri)

Two patents with Kabuki Syndrome Presenting with endocrine problems

Journal of Pediatric Endocrinology and Metabolism, ss.215-220, 2001 (Diğer Kurumların Hakemli Dergileri)

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

Marmara Medical Journal, cilt.12, ss.98-100, 1999 (Diğer Kurumların Hakemli Dergileri) identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

DISORDER OF ADRENAL EXCESS AND ADRENAL MEDULLA

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 Şubat 2018 - 01 Mart 2108

Hypocalcem a and Hypercalcem a in Children

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

Rare Causes of Osteogenesis Imperfecta are Commonin Consanguineous Pedigrees

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

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

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Avusturya, 19 - 21 Eylül 2019, cilt.91

A rare cause of hypophosphatemia: Raine Syndrome

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Avusturya, 19 - 21 Eylül 2019, cilt.91

A Case Of Syndromic Hypopituitarism

European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, 19 - 21 Eylül 2019, cilt.91, ss.1-682 identifier identifier identifier

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, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.623-624 identifier

Psödohipoparatiroidi Uzlaşı Raporu

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 17 - 21 Nisan 2019

Pediatrik Tiroid Kanserlerine Yaklaşım

15. Türk Rinoloji Kongresi, 7.Ulusal Otoloji Nörootoloji Kongresi ve 3.Ulusal Baş Boyun Cerrahisi Kongresine, Türkiye, 4 - 07 Nisan 2019

Çocuklukta Osteogenesis İmperfekta Klinik Yaklaşım ve Tedavide İlkeler :

3.Ege Endokrin Hastalıklar ve Genetik Sempozyumu, Türkiye, 7 - 09 Mart 2019

Congenital Adrenal Hyperplasia

ESPE Winter School, 22 - 28 Şubat 2019

Disorders of sexual differentiation

Disorders of sexual differentiation, 22 - 28 Şubat 2019

Introduction to molecular endocrinology

ESPE Winter School, 22 - 28 Şubat 2019

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

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

Psödohipoparatiroidi tanı ve tedavisi

Pediatrik Endokrinoloji İleri Kursu, Türkiye, 2 - 04 Kasım 2018

Düşük renin düzeyi: endokrin hipertansiyon

Çocuk Endokrinolojisi Olgu Sunumları-9, İstanbul, Türkiye, 19 - 20 Ekim 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 Ekim 2018

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

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

Nationwide Hypophosphatemic Rickets Study

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

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

28th International Congress of the European-Respiratory-Society (ERS), Paris, Fransa, 15 - 19 Eylül 2018, cilt.52 identifier

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, 27 - 29 Eylül 2018, cilt.90, ss.597

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 Eylül 2018, cilt.90, ss.568

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 Eylül 2018, cilt.90, ss.514

Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Türkiye, 18 - 22 Nisan 2018

BOY KISALIĞINA GENEL YAKLAŞIM

İSKELETİN GENETİK HASTALIKLARI KURSU, Türkiye, 18 Nisan 2018

Düşük Alkali Fosfotaz Düzeyinin Önemi

40. Pediatri Günleri ve 19. Pediatri Hemşireliği Günleri, Türkiye, 8 - 11 Nisan 2018

INTRODUCTION TO MOLECULAR ENDOCRINOLOGY

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 Şubat - 01 Mart 2018

DISORDER OF SEXUEL DEVELOPMENT

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 Şubat - 01 Mart 2018

CONGENITAL ADRENAL HYPERPLASIA

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 Şubat - 01 Mart 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, 14 - 17 Eylül 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 Eylül 2017, cilt.88, ss.54

Disorders of sexual differentiation

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

Disorders of adrenocortical excess and adrenal medulla

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

Congenital Adreal Hyperplasia

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

Introduction to molecular endocrinology

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

Neonatal Hypocalcemia

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

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

55th Annual Meeting of the ESPE, Paris, 10 - 12 Eylül 2016, cilt.86, ss.175-176

Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta

55th Annual Metting of the ESPE Paris, 10 - 12 Eylül 2016, cilt.86, ss.167

Reconsideration of Mid Parental Height Calculation

55th Annual Meeting of the ESPE, 10 - 12 Eylül 2016, cilt.86, ss.451

Current Perspective on Pseudohypoparathyroidism New Classification

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

Late Breaking news

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

CAH Congenital Adrenal Hyperplasia

ESPE Winter School, 18 - 24 Mart 2016

Disorders of SExual Differentiation

ESPE Winter School, 18 - 24 Mart 2016

Introduction to Molecular Endocrinology

ESPE Winter School, 18 - 24 Mart 2016

HPP Genel Değerlendirme

HİPOFOSFATAZYA DANIŞMA KURULU TOPLANTISI, Türkiye, 16 Aralık 2015

HİPOTİROİDİ VE TİROTOKSİKOZUN YENİDOĞAN ÜZERİNE ETKİSİ

GEBELİK VE TİROİD SEMPOZYUMU, Türkiye, 12 Aralık 2015

Diyabet ile yaşam

Diyabet ile Yaşam- Cerrahpaşa, Türkiye, 13 Kasım 2015

Growth Hormone Deficiency and Treatment

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

Piknodisostozis Otorinolaringolojik bulgular

37. TÜRK ULUSAL KULAK BURUN BOĞAZ VE BAŞ BOYUN CERRAHİSİ KONGRESİ, Türkiye, 28 Ekim - 01 Kasım 2015

Nonklasik Konjenital Adrenal Hiperplazi Hastalarının Genotip Ve Fenotip Özellikleri

19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Türkiye, 22 - 24 Ekim 2015

Periferal Puberte Prekokslu 129 Çocukta Etiyolojik Dağılım Ve Klinik Özellikler

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 22 - 24 Ekim 2015

Temel genetik kavramlar ve kalıtım şekilleri

1. Pediatrik Endokrinolojiye Giriş Kursu, Türkiye, 21 - 22 Ekim 2015

Merkezi Yenidogan Tarama Programi ile Tani Almis Konjenital Hipotiroidili Vakalarimizin İzlemi

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 22 - 24 Ekim 2015

Otozomal Resesif Osteogenezis İmperfekta Populasyonumuzdaki Sıklığı Ve Genetik Nedenleri

19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Türkiye, 22 - 24 Ekim 2015

YILLIK

19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 22 - 24 Ekim 2015

Friedreich s Ataxia Presenting with Diabetes Mellitusin an Adolescent

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

Factors Effecting Response to Growth HormoneTreatment in Children with Turner Syndrome

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

Dysosteosclerosis from a unique mutation in SLC29A3

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

ANTLEY BİXLER SENDROMLU BİR OLGUMUZ

Cocuk Endokrinoloji Dernegi 7.Olgu Sunumlari Toplantisi, İzmir, Türkiye, 18 - 20 Mayıs 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 Ekim 2015

GEÇ ÇOCUKLUK ERKEN ERGENLİK

KANUNİ SULTAN SÜLEYMAN GÜNLERİ, Türkiye, 20 - 21 Şubat 2015

Dysosteosclerosis: Evidence for Genetic Heterogeneity

Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, Texas, Amerika Birleşik Devletleri, 12 - 15 Eylül 2014, cilt.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, Amerika Birleşik Devletleri, 4 - 07 Ekim 2013, cilt.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 Aralık 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, Amerika Birleşik Devletleri, 16 - 19 Eylül 2007, cilt.22 identifier

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

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.125-126 identifier

Kitap & Kitap Bölümleri

Hipofosfatemik Rikets veDiğer Herediter Rikets Türleri

Yurdakök Pediatri, Murat Yurdakök, Editör, Güneş, ss.4055-4072, 2017

GNAS Complex Locus

Encyclopedia of Signaling Molecules, Sangdun Choi, Editör, Springer New York, New-York, ss.1-13, 2017

Bilirkişi Raporları