SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 Years
Journal of Clinical Research in Pediatric Endocrinology
, cilt.15, sa.2, ss.154-159, 2023 (SCI-Expanded)
Basal cortisol measurements in the prediction of low-dose ACTH stimulation test outcomes
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.139, 2022 (SCI-Expanded)
Etiological analysis of hypophosphatemia: A single-center experience
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.141-142, 2022 (SCI-Expanded)
Change of menarcheal age in schoolgirls living in Istanbul over the last 12 years
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.364, 2022 (SCI-Expanded)
Breast ultrasonography: How useful in the diagnosis of precocious puberty?
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.46-47, 2022 (SCI-Expanded)
Glucagon response to hypoglycemia during extended oral glucose tolerance test in children with cystic fibrosis and comparing with healthy peers
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.199-200, 2022 (SCI-Expanded)
Low-dose ACTH Stimulation Test: Comparison of Cortisol Response at 30, 40, and 60 Minutes
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.117-118, 2022 (SCI-Expanded)
Single Nucleotide Polymorphisms (SNPs) Profile as Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.231-232, 2022 (SCI-Expanded)
A Case of Short Stature Presenting with Multiple Exocytosis
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.318, 2022 (SCI-Expanded)
A rare cause of monogenic obesity: Schaaf-Yang syndrome due to a novel MAGEL2 gene variant
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.230, 2022 (SCI-Expanded)
Circulating mRNA and miRNA Signatures as Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.213, 2022 (SCI-Expanded)
Differences due to the variant type in the inheritance pattern of BMP15 gene-related primary ovarian insufficiency: a girl with a homozygous null BMP15 gene variant
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.377-378, 2022 (SCI-Expanded)
Diagnostic Features and Risk Factors for Childhood Thyroid Cancers
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.407, 2022 (SCI-Expanded)
Wide phenotypical spectrum with the same karyotype: Mixed gonadal dysgenesis
Seven Menevşe T., Gürpınar Tosun B., Helvacioglu D., Abali Z. Y., Kirmizibekmez H., Dursun F., et al.
HORMONE RESEARCH IN PAEDIATRICS
, cilt.95, sa.SUPPL 2, ss.566, 2022 (SCI-Expanded)
Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high normal testicular volume
SEXUAL DEVELOPMENT
, cilt.16, sa.SUPPL 1, ss.61-62, 2022 (SCI-Expanded)
Rahman Syndrome: Hypopituitarism might be responsible for changing height pattern
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.359, 2021 (SCI-Expanded)
Biallelic PPP2R3C mutations are associated with partial and complete gonadal dysgenesis in 46,XY and 46,XX individuals
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.92, 2021 (SCI-Expanded)
Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.64-65, 2021 (SCI-Expanded)
A rare cause of hypercalcemia: Congenital Lactase Deficiency
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.75, 2021 (SCI-Expanded)
Clinical and hormonal evolution of aldosterone synthase deficiency: Is complete remission possible?
Gürpınar Tosun B., Demirkol Y. K., Seven Menevşe T., Kaygusuz S. B., Ozbek M. N., Altıncık S. A., et al.
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.184-185, 2021 (SCI-Expanded)
Severe Hypophosphatemic Rickets due to Tumor-Induced Osteomalasia
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.209, 2021 (SCI-Expanded)
Is quail egg a potential endocrine disruptor?
Sürekli Karakuş Ö., Arabacı Tamer S., Levent H. N., Kaygusuz S. B., Demircioğlu S., Akakın D., et al.
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.364, 2021 (SCI-Expanded)
Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.75, 2021 (SCI-Expanded)
46,XY DSD due to biallelic DHX37 gene mutations
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.393-394, 2021 (SCI-Expanded)
Machine Learning Quest for Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.275, 2021 (SCI-Expanded)
Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17 alpha-Hydroxylase/17,20-Lyase Deficiency
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.191, 2021 (SCI-Expanded)
Correlation of 11-oxygenated C19 androgens with the clinical and biochemical characteristics in premature adrenarche
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.120-121, 2021 (SCI-Expanded)
Hyperinsulinemic hypoglycemia due to biallelic mutations in the DNAJC3 gene
HORMONE RESEARCH IN PAEDIATRICS
, cilt.94, sa.SUPPL 1, ss.107, 2021 (SCI-Expanded)
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
, cilt.12, sa.2, ss.150-159, 2020 (SCI-Expanded)
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, sa.10, ss.1243-1250, 2019 (SCI-Expanded)
Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.205-206, 2019 (SCI-Expanded)
Age of obesity onset could be the first indicator of future metabolic complications - preliminary data of prospective multicenter study
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.153-154, 2019 (SCI-Expanded)
Evaluation of brain MRI lesions in 381 girls with central precocious puberty
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.329-330, 2019 (SCI-Expanded)
Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.215, 2019 (SCI-Expanded)
Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.214, 2019 (SCI-Expanded)
Cushing Syndrome due to an adrenacortical carcinoma in a baby with atypical Beckwith-Wiedemann Syndrome
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.371, 2019 (SCI-Expanded)
Simplifying the interpretation of steroid metabolome data by a machine-learning approach
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.128, 2019 (SCI-Expanded)
A Case Of Syndromic Hypopituitarism
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.589, 2019 (SCI-Expanded)
A rare cause of hypophosphatemia: Raine Syndrome
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.384, 2019 (SCI-Expanded)
Hypergonadotropic hypogonadism in 46, XX adolescents without gonadotoxic therapy: Clinical features and molecular etiologies
HORMONE RESEARCH IN PAEDIATRICS
, cilt.91, ss.265, 2019 (SCI-Expanded)
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, sa.8, ss.3049-3067, 2019 (SCI-Expanded)
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, sa.2, ss.229-236, 2019 (SCI-Expanded)
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
Journal of clinical research in pediatric endocrinology
, cilt.11, sa.2, ss.149-156, 2019 (SCI-Expanded)
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, sa.4, ss.336-342, 2018 (SCI-Expanded)
THE CO-EXISTENCE OF TWO RARE DISEASES: A CASE REPORT
PEDIATRIC NEPHROLOGY
, cilt.33, sa.10, ss.1881, 2018 (SCI-Expanded)
The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience
Journal of clinical research in pediatric endocrinology
, cilt.10, sa.2, ss.125-130, 2018 (SCI-Expanded)
Diagnosis and Management of Pseudohypoparathyroidism and Related Disorders: First International Consensus Statement
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.108-109, 2018 (SCI-Expanded)
Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.597, 2018 (SCI-Expanded)
An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.514, 2018 (SCI-Expanded)
Delayed Diagnosis of a Patient with Antley-Bixler Syndrome
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.166-167, 2018 (SCI-Expanded)
Persistent Mullerian duct syndrome: Rare But Important Aetiology of an Inguinal Hernia and Cryptorchidism in Boys
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.568, 2018 (SCI-Expanded)
Recurrent Hypoglycemia in a Preschooler Girl with Overgrowth: Isolated ACTH-Deficiency with a Novel TPIT Mutation
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.132, 2018 (SCI-Expanded)
An Unusual Cause of Short Stature
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.184-185, 2018 (SCI-Expanded)
Nationwide Hypophosphatemic Rickets Study
HORMONE RESEARCH IN PAEDIATRICS
, cilt.90, ss.109-110, 2018 (SCI-Expanded)
CLINICAL CHARACTERISTICS OF TURKISH CHILDREN AND ADOLESCENTS WITH TYPE 2 DIABETES
HORMONE RESEARCH IN PAEDIATRICS
, cilt.88, ss.282, 2017 (SCI-Expanded)
CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY
HORMONE RESEARCH IN PAEDIATRICS
, cilt.88, ss.313-314, 2017 (SCI-Expanded)
Reconsideration of Mid-Parental Height Calculation
HORMONE RESEARCH IN PAEDIATRICS
, cilt.86, ss.451, 2016 (SCI-Expanded)
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-Expanded)
beta-hCG from an Occult Source Causing Peripheral Precocious Puberty: Identification of the Tumour 6 Years After Presentation
HORMONE RESEARCH IN PAEDIATRICS
, cilt.86, ss.428, 2016 (SCI-Expanded)
Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes
HORMONE RESEARCH IN PAEDIATRICS
, cilt.86, ss.175-176, 2016 (SCI-Expanded)
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, sa.3, ss.183-191, 2015 (SCI-Expanded)
Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
, cilt.7, sa.2, ss.98-101, 2015 (SCI-Expanded)
Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
, cilt.7, sa.1, ss.27-36, 2015 (SCI-Expanded)
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, sa.1, ss.37-44, 2015 (SCI-Expanded)
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, sa.4, ss.182-186, 2014 (SCI-Expanded)
Sleep disordered breathing in pycnodysostosis patients
EUROPEAN RESPIRATORY JOURNAL
, cilt.44, 2014 (SCI-Expanded)
Sleep disordered breathing in children with endocrinological problems
EUROPEAN RESPIRATORY JOURNAL
, cilt.44, 2014 (SCI-Expanded)
Evaluation of bone metabolism in patients receiving home ventilation
EUROPEAN RESPIRATORY JOURNAL
, cilt.42, 2013 (SCI-Expanded)
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, sa.10, ss.3633-3639, 2009 (SCI-Expanded)
Alopecia: Association with resistance to thyroid hormones
Journal of Pediatric Endocrinology and Metabolism
, cilt.22, sa.11, ss.1075-1081, 2009 (SCI-Expanded)
A novel missense mutation in the first extracellular loop of the neurokinin B receptor causes hypogonadotropic hypogonadism
HORMONE RESEARCH
, cilt.72, ss.402, 2009 (SCI-Expanded)
Final height in girls with idiopathic precocious puberty treated with leuprolide: dose-titration approach
HORMONE RESEARCH
, cilt.72, ss.123, 2009 (SCI-Expanded)
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, sa.8, ss.745-51, 2008 (SCI-Expanded)
Polymorphisms in the vitamin D receptor gene in children with idiopathic hypercalcemia
HORMONE RESEARCH
, cilt.70, ss.49, 2008 (SCI-Expanded)
Identification of a novel dentin matrix protein-1 (DMP-1) mutation in a kindred with autosomal recessive hypophosphatemia and dental anomalies
HORMONE RESEARCH
, cilt.70, ss.184-185, 2008 (SCI-Expanded)
Alopecia areata: A new association with resistance to thyroid hormones in a family with novel TRb mutation
HORMONE RESEARCH
, cilt.70, ss.57, 2008 (SCI-Expanded)
Long-term follow-up of a patient with pituitary resistance to thyroid hormones: Comparison of D-thyroxine and triiodothyroacetic acid treatments
HORMONE RESEARCH
, cilt.70, ss.59-60, 2008 (SCI-Expanded)
Genetic testing of Turkish patients with pseudohypoparathyroidism type Ib
HORMONE RESEARCH
, cilt.70, ss.50, 2008 (SCI-Expanded)
Hypophosphatemic rickets: New and important roles for bone mineralization and phosphate homeostasis of Dentin matrix protein-1
HORMONE RESEARCH
, cilt.70, ss.14, 2008 (SCI-Expanded)
Familial thyroid dysgenesis: Which genes could be involved?
HORMONE RESEARCH
, cilt.70, ss.163, 2008 (SCI-Expanded)
Screening of parents and siblings of children with thyroid dysgenesis by thyroid function tests and ultrasound
HORMONE RESEARCH
, cilt.65, ss.41, 2006 (SCI-Expanded)
Pycnodysostosis: A rare cause of short stature
HORMONE RESEARCH
, cilt.65, ss.76, 2006 (SCI-Expanded)
Factors related to childhood obesity
HORMONE RESEARCH
, cilt.65, ss.82, 2006 (SCI-Expanded)
Evaluation of patients with Graves' disease
HORMONE RESEARCH
, cilt.65, ss.41, 2006 (SCI-Expanded)
Factors associated with obesity in children with hypothalamo-pituitary tumors
HORMONE RESEARCH
, cilt.65, ss.83, 2006 (SCI-Expanded)
Diğer Dergilerde Yayınlanan Makaleler
Renal agenezisi olan bir Beckwith-Wiedemann Olgusu
TURKISH NEPHROLOGY, DIALYSIS AND TRANSPLANTATION JOURNAL
, cilt.16, ss.196-197, 2007 (ESCI)
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar
DISORDER OF ADRENAL EXCESS AND ADRENAL MEDULLA
EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, Cairo, Mısır, 23 Şubat - 01 Mart 2018
Osteogenezis İmperfekta’da Tedavi- Multidisipliner Yaklaşım Çocuk Endokrin Uzmanı Bakış Açısı
25. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 09 Ekim 2021
Toplumumuzda Osteogenezis İmperfektada Genetik Nedenler ve Genotip Fenotip İlişkisi.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi. , Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-2
DNAJC3 Genindeki Bialelik Mutasyona Bağlı Hiperinsülinemik Hipoglisemi
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-2
Prematür adrenarş tanılı kız çocuklarında 11-oksiandrojenlerin klinik ve biyokimyasal parametrelerle ilişkisi.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi., Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-3
İnsülin Degludek/Aspart ile Az Çoktur !
25. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 06 Ekim 2021
Adrenokortikal hormon profilleri: KAH dışı primer adrenal yetmezlikte moleküler etiyolojiyi öngörebilir mi?
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi. , Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-2
Düşük Doz ACTH Uyarı Testinde 30, 40 ve 60. Dakikalardaki Kortizol Yanıtının Karşılaştırılması.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi. , Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-3
Bıldırcın Yumurtası Bir Endokrin Bozucu mudur?
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-3
Toplumumuzda Osteogenezis İmperfektada Genetik Nedenler ve Genotip Fenotip İlişkisi
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Türkiye, 06 Ekim 2021
PARATİROİD HASTALIKLARI VE YÖNETİMİ
VI. Pediatrik Endokrinoloji İleri Kursu, 11 Haziran 2021
Pediatrik hastalarda IDegAsp kullanımı ile ilgili esaslar nelerdir?
42. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, 20 Mayıs 2021
NEONATAL DİYABETES MELLITUS İLE PREZENTE OLAN LRBA EKSİKLİĞİ: ABATACEPT DENEYİMİ.
10. OLGU SUNUMLARI, İzmir, Türkiye, 9 - 10 Nisan 2021, ss.1-2
KLİTEROMEGALİNİN ENDER BİR NEDENİ: APENDEKTOMİ SONRASI GELİŞEN KLİTORAL PRİAPİSM.
10. OLGU SUNUMLARI, İzmir, Türkiye, 9 - 10 Nisan 2021, ss.1-2
NADİR BİR HİPERKALSEMİ NEDENİ: KONJENITAL LAKTAZ EKSİKLİĞİ.
10. OLGU SUNUMLARI, İzmir, Türkiye, 9 - 10 Nisan 2021, ss.1-2
BOY KISALIĞI İLE BAŞVURAN KIRIK ÖYKÜSÜ OLMAYAN OSTEOGENEZİS İMPERFEKTA OLGUSU.
10. OLGU SUNUMLARI, İzmir, Türkiye, 9 - 10 Nisan 2021, ss.1-2
PSÖDOHİPOPARATİROİDİ TANILI HASTADA VENÖZ KALSİFİKASYON TEDAVİSİNDE ASETOZOLAMİD KULLANIMI.
10. OLGU SUNUMLARI, İzmir, Türkiye, 9 - 10 Nisan 2021, ss.1-2
46, XY GONADAL DİSGENEZİLİ OLGUDA NR5A1 VE DHX37 GENLERİNDE DİGENİK MUTASYONLAR.
10. OLGU SUNUMLARI, İzmir, Türkiye, 9 - 10 Nisan 2021, ss.1-2
SLC29A3 MUTASYONUNA BAĞLI HASTALIK SPEKTRUMU: DİSOSTEOSKLEROZİSDEN H SENDROMUNA
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Türkiye, 12 - 13 Mart 2021, ss.1-2
PREPUBERTAL JİNEKOMASTİLİ OLGUDA AROMATAZ FAZLALIĞI.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Türkiye, 12 - 13 Mart 2021, ss.1-2
OSTEOGENEZİS İMPERFEKTA ÖN TANISIYLA SEVK EDİLEN OLGUDA SAPTANAN NADİR BİR İSKELET DİSPLAZİSİ: KAMPOMELİK DİSPLAZİ.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Türkiye, 12 - 13 Mart 2021, ss.1-2
BMP15 GENİ İLE İLİŞKİLİ OVER DİSGENEZİSİNDE MUTASYON TİPİNE GÖRE KALITIM PATERNİ DEĞİŞİYOR MU?
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu., İzmir, Türkiye, 12 - 13 Mart 2021, ss.1-2
Hyperthyroidism
ESPE Winter School Online, 27 Şubat 2021
Congenital adrenal hyperplasia
ESPE Winter School Online, 27 Şubat 2021
Bıldırcın Yumurtası Bir Endokrin Bozucu Mudur?
8. Marmara Pediatri Kongresi. , İstanbul, Türkiye, 20 - 21 Şubat 2021, ss.1-2
Prader Willi Sendromlu Hastalarımızın Genetik, Endokrinolojik, Polisomnografik ve Otolaringolojik Değerlendirme Sonuçları
8. Marmara Pediatri Kongresi, İstanbul, Türkiye, 20 Şubat - 21 Mart 2021, ss.109-110
Klasik tip 21 hidroksilaz eksikliğine bağlı konjenital adrenal hiperplazi tanılı olgularda puberte özellikleri,pubertal boy kazanımı ve final boya etki eden faktörlerin değerlendirilmesi: çok merkezli çalışma
XXIV.Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi, Türkiye, 30 Ekim - 01 Kasım 2020, ss.34
Steroid 11β-hidroksilaz eksikliği olan 100 çocuk hastanın klinik bulgularının genetik ve adrenokortikal hormon profili ile ilişkisinin değerlendirilmesi
XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi, Türkiye, 30 Ekim - 01 Kasım 2020
Bone related-comorbidities in children and adults with genetic conditions
European Calcified Tissue Society 2020 Digital Congress, Marseille, Fransa, 22 - 24 Ekim 2020
Oturum başkanlığı
Çocukluk çağı Nefro-endokrin hastalıklar sempozyumu, İstanbul, Türkiye, 2 - 03 Ekim 2020
Büyümenin Değerlendirilmesi
BAŞKENT ÜNİVERSİTESİ İSTANBUL UYGULAMA VE ARAŞTIRMA MERKEZİ ÇOCUK SAĞLIĞI VE HASTALIKLARI ANA BİLİM DALI İSTANBUL TOPLANTISI Pediatride Güncel Yaklaşımlar II, İstanbul, Türkiye, 08 Şubat 2020
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
Simplifying the interpretation of steroid metabolome data by a machine-learning approach
The 58th Annual ESPE Meeting, 19 - 21 Eylül 2019, cilt.91, ss.128
Efficacy and safety of liraglutide vs placebo in children and adolescents with type 2 diabetes: the ellipse randomised trial results
DIABETOLOGIA, Barcelona, İspanya, 16 - 20 Eylül 2019, cilt.62, ss.44
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
Yenidoğanda Nadir Bir Hiperkalsemi nedeni : Kalsiyum Duyarlı Reseptör Mutasyonuna bağlı Ağır neonatal Hiperparatiroidizm
27. Ulusal Neonatoloji Kongresi, Antalya, Türkiye, 3 - 07 Nisan 2019
Çocuklukta Osteogenesis İmperfekta Klinik Yaklaşım ve Tedavide İlkeler :
3.Ege Endokrin Hastalıklar ve Genetik Sempozyumu, Türkiye, 7 - 09 Mart 2019
Segmental Aşırı büyüme kliniği olan olguda somatik PIK3CA mutasyonu
3. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Türkiye, 7 - 09 Mart 2019
Disorders of adrenocortical excess and adrenal medulla
ESPE Winter School, 22 - 28 Şubat 2019
Introduction to molecular endocrinology
ESPE Winter School, 22 - 28 Şubat 2019
Congenital Adrenal Hyperplasia
ESPE Winter School, 22 - 28 Şubat 2019
Disorders of sexual differentiation
Disorders of sexual differentiation, 22 - 28 Şubat 2019
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
Persistan Mullerian Duct Syndrome: Rare but impotant aetiology of an inguinal hernia and cryptorchidism in boys
57th Annual European Society for Paediatric Endocrinology(ESPE), Athens, Yunanistan, 27 - 29 Eylül 2018
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
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, Yunanistan, 27 - 29 Eylül 2018, cilt.90, ss.597
Recurrent Hypoglycemia in a Preschooler Girl with Overgrowth: Isolated ACTH-Deficiency with a Novel TPIT Mutation
HORMONE RESEARCH IN PAEDIATRICS, Athens, Yunanistan, 27 - 29 Eylül 2018, cilt.90, ss.132
KEMİK MİNERAL DENSİTE YÜKSEKLİĞİ İLE KARAKTERİZE İSKELETİN GENETİK HASTALIKLARI
İSKELETİN GENETİK HASTALIKLARI KURSU, Türkiye, 18 Nisan 2018
KEMİK MİNERAL DANSİTE DÜŞÜKLÜĞÜ İLE KARAKTERİZE İSKELETİN GENETİK HASTALIKLATI
İSKELETİN GENETİK HASTALIKLARI KURSU, Türkiye, 18 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
Relation of serum IGF-1 and IGFBP3 levels with acute exacerbaion in cystic fibrosis
2nd Annual Middle East Cystic Fibrosis Congress, İzmir, Türkiye, 22 - 23 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
INTRODUCTION TO MOLECULAR ENDOCRINOLOGY
EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, 23 Şubat - 01 Mart 2018
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, Amerika Birleşik Devletleri, 14 - 17 Eylül 2017
CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY.
IMPE 2017, 14 - 17 Eylül 2017
Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency
American Association of Clinical Chemistry Congress, Washington, Amerika Birleşik Devletleri, 30 Temmuz - 03 Ağustos 2017
Congenital Adreal Hyperplasia
European Society for Paediatric Endocrinology-Winter School, 10 - 16 Şubat 2017
Disorders of sexual differentiation
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
Disorders of adrenocortical excess and adrenal medulla
European Society for Paediatric Endocrinology Winter School, 10 - 16 Şubat 2017
Çocukluk çağındaki over kisti vakalarının incelenmesi: çok merkezli çalışma
16. Ulusal Pediatrik Endokrinoloji Kongresi, Türkiye, 8 - 10 Kasım 2012
From Pseudohypoparathyroidism to Inactivating PTH PTHrP Signaling Disorder iPPSD a Novel Classification Proposed by the European EuroPHP Network
55th Annual Meeting of the ESPE, 10 - 12 Eylül 2016, cilt.86, ss.31
Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine
55th Annual Meeting of the ESPE, 10 - 12 Eylül 2016, cilt.86, ss.244
The Effect of Subclinical Hypothyroidism SH and Treatment of SH with L T4 on Basal Metabolic Rate in Obese Children A Prospective Study
55th Annual Meeting of the ESPE, Paris, 10 - 12 Eylül 2016, cilt.86, ss.303
beta hCG from an Occult Source Causing Peripheral Precocious Puberty Identification of the Tumour 6 Years After Presentation
55th Annual Meeting of the ESPE, 10 - 12 Eylül 2016, cilt.86, ss.428
A European Survey to Identify New Roads for Care Training and Research Around Rare Metabolic Bone Diseases
55th Annual Meeting of the ESPE, Paris, 10 - 12 Eylül 2016, cilt.86, ss.169
Reconsideration of Mid Parental Height Calculation
55th Annual Meeting of the ESPE, 10 - 12 Eylül 2016, cilt.86, ss.451
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
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
Disorders of SExual Differentiation
ESPE Winter School, 18 - 24 Mart 2016
CAH Congenital Adrenal Hyperplasia
ESPE Winter School, 18 - 24 Mart 2016
Introduction to Molecular Endocrinology
ESPE Winter School, 18 - 24 Mart 2016
Disoerder of Adrenocortical Excess and Adrenal Medulla
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
Diagnostic and prognostic value of serum urokinase plasminogen activation receptor supar procalcitonin pct and C reactİve protein CRP in children with SIRS sepsis and febrile neutropenia
9th World Congress on Pediatric Infectious Diseases, Rio-De-Janeiro, Brezilya, 18 - 21 Kasım 2015
Diagnostic and prognostic value of serum urokinase plasminogen activation receptor SUPAR procalcitonin PCT abd C reactive protein CRP in children with SIRS sepsis and febrile neutropenia
9th World Congress of the World Society for Pediatric Infectious Diseases (WSPID), 18 - 21 Kasım 2015
DIAGNOSTIC AND PROGNOSTIC VALUE OF SERUM UROKINASE PLASMINOGEN ACTIVATIONRECEPTOR SUPAR PROCALCITONIN PCT AND C REACTIVE PROTEIN CRP IN CHILDREN WITHSIRS SEPSIS AND FEBRILE NEUTROPENIA
The 9th World Congress of the World Society for Pediatric Infectious Diseases, Rio de Janeiro, Brazil, 18 - 21 Kasım 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
Temel genetik kavramlar ve kalıtım şekilleri
1. Pediatrik Endokrinolojiye Giriş Kursu, Türkiye, 21 - 22 Ekim 2015
Serbest T4 Düşük TSH Hafif Yüksek Olgularda Santral Hipotiroidi Primer Hipotiroidi Ayrımını Nasıl Yapabiliriz
19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 22 - 24 Ekim 2015
Ulusal Düzeyde Noonan Sendromlu Olgularin Klinik Özellikleri ve Büyüme İzlemlerinin Değerlendirilmesi
19. ÇOCUK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Türkiye, 22 - 24 Ekim 2015
Merkezi Yenidogan Tarama Programi ile Tani Almis Konjenital Hipotiroidili Vakalarimizin İzlemi
19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 22 - 24 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
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, İspanya, 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
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, İspanya, 1 - 03 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), Barcelona, İspanya, 1 - 03 Ekim 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, İspanya, 1 - 03 Ekim 2015
ANTLEY BİXLER SENDROMLU BİR OLGUMUZ
Cocuk Endokrinoloji Dernegi 7.Olgu Sunumlari Toplantisi, İzmir, Türkiye, 18 - 20 Mayıs 2015
ÇOCUKLARDA SIRS SEPSİS VE FEBRİL NÖTROPENİDE SERUM UROKİNAZPLAZMİNOJEN AKTİVATÖR RESEPTÖR SUPAR PROKALSİTONİN PCT VE CREAKTİFPROTEİNİN CRP DİAGNOSTİK VE PROGNOSTİK DEĞERİNİN ARAŞTIRILMASI
9. Ulusal Çocuk Enfeksiyon Hastalıkları Kongresi, Türkiye, 5 - 08 Nisan 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
Hyperglycemia During Cooling: Is it a Rare Complication?
4th International Congress of UENPS, ATİNA, Yunanistan, 11 - 14 Aralık 2014
Hyperglicemia during cooling is it a rare complications
4th International Congress of UENPS, 11 Aralık 2014
Hipoglisemi: Kistik Fibrozise bağlı diyabet tanısında CGMS (sürekli glukoz izleme sistemi) ile OGTT nin karşılaştırılması
TTD 17. yıllık kongresi, Antalya, Türkiye, 2 - 06 Nisan 2014
Evaluation of bone metabolism in patients receiving home ventilation
23th European Respiratory Society Meeting, 7 - 11 Eylül 2013
Cystic fibrosis related osteopenia: what is the etiology?
23th European Respiratory Society Meeting, 7 - 11 Eylül 2013
Neonatal hipertrofik kardiyomiyopatiye neden olan homozigot bir TMEM70 mutasyonu
20. Ulusal Neonatoloji Kongresi, Türkiye, 15 - 18 Nisan 2012
Maternal Thyroid Dysfunction and Neonatal Problems
2nd Interanational Congress of UENPS, İstanbul, Türkiye, 15 - 17 Kasım 2010
Kitap & Kitap Bölümleri
Hipofosfatemik Raşitizm
Çocuk Endokrinolojisi Ve Diyabet, Darendeliler Feyza, Zehra Aycan, Cengiz Kara, Samim Özen, Erdal Eren, Editör, İstanbul Tıp Kitabevi, İstanbul, ss.1874-1900, 2021
Hipokalsemi
Çocuk Endokrinolojisi ve Diyabet, Darendeliler Feyza, Zehra Aycan, Cengiz Kara, Samim Özen, Erdal Eren, Editör, İstanbul Tıp Kitabevi, İstanbul, ss.1748-1773, 2021
İnsülin benzeri büyüme faktorü (IGF-I) ve IGF baglayici protein (IGFBP-3)‘ün klinikte kullanimi
Çocuk ve Adolesanda Endokrin Testler, , N. Yordam,A. Alikasifoglu ve A. Bideci, Editör, Güneş Kitabevi, Ankara, ss.23-48, 2006