Travaux scientifiques

Prof. Dr. Peyami Cinaz

183 publications. La source de l’information est indiquée à côté de chaque publication.

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  1. Early Cardiometabolic Characteristics in Childhood Among Large-for-Gestational-Age Infants

    Pediatric Practice and Research, 2026

    DOI 10.21765/pprjournal.1974143 Texte intégral en libre accèsSource : OpenAlex

  2. Vitamin D, Insulin Resistance and Cytokine Levels in Obese Pubertal Children

    The Journal of Pediatric Academy, 2023

    DOI 10.4274/jpea.2023.213 Source : OpenAlex

  3. Kistik Fibroziste Endokrin Sistem Tutulumu ve Tedavi Yaklaşımları

    2021

    Source : OpenAlex

  4. The effect of beta-glucan supplementation on glycemic control and variability in adolescents with type 1 diabetes mellitus

    Diabetes Research and Clinical Practice, 2020

    DOI 10.1016/j.diabres.2020.108464 PMID 32971156 16 citations (Europe PMC) Source : OpenAlex

  5. Diagnostic value of urinary luteinizing hormone levels in the monitoring of precocious puberty treatment

    Archives of Endocrinology and Metabolism, 2020

    DOI 10.20945/2359-3997000000212 PMID 32236310 11 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  6. Kistik Fibrozis ile İlişkili Diyabet: Bir Olgu Sunumu

    Journal of Nutrition and Dietetics, 2020

    DOI 10.33076/2020.bdd.1346 Source : OpenAlex

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

    Diabetic Medicine, 2019

    DOI 10.1111/dme.14038 PMID 31099079 6 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  8. Congenital Generalized Lipodystrophy Type 4 - New Mutation in the CAVIN1 Gene

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Source : OpenAlex

  9. Evaluation of the Association of Glutamic Acid Decarboxylase Antibody and Limbic Encephalitis in Children with Type 1 Diabetes Mellitus

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Source : OpenAlex

  10. Cinacalcet Experience in Hypercalcemia Due to CaSR Mutation

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Source : OpenAlex

  11. A Case of Panhipopituitarism with SOX3 Gene Deletion

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Source : OpenAlex

  12. Long-Term Honeymoon Period in Type 1 Diabetes: True Diagnosis MODY5; New Mutation of HNF1B

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Source : OpenAlex

  13. Relationship between obesity and iron deficiency anemia: is there a role of hepcidin?

    Hematology, 2018

    DOI 10.1080/10245332.2018.1423671 PMID 29318945 34 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  14. Effect of Telehealth System on Glycemic Control in Children and Adolescents with Type 1 Diabetes

    Journal of Clinical Research in Pediatric Endocrinology, 2018

    DOI 10.4274/jcrpe.0017 PMID 30015620 30 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  15. Anxiety and depression states of adolescents with polycystic ovary syndrome

    TURKISH JOURNAL OF MEDICAL SCIENCES, 2018

    DOI 10.3906/sag-1708-131 PMID 29914248 24 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  16. Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing

    TURKISH JOURNAL OF MEDICAL SCIENCES, 2018

    DOI 10.3906/sag-1711-74 PMID 29714459 6 citations (Europe PMC) Source : OpenAlex

  17. Vitamin D status and premature adrenarche

    Pediatrics International, 2018

    DOI 10.1111/ped.13682 PMID 30129969 4 citations (Europe PMC) Source : OpenAlex

  18. Clinical and Epidemiological Features of Children with Type 1 Diabetes

    57th Annual ESPE, 2018

    Source : OpenAlex

  19. The Levels of Blood Glucose and Counting of Carbohydrate-Fat-Protein in Diabetic Children Using Pump with Aspart and Glulisine

    57th Annual ESPE, 2018

    Source : OpenAlex

  20. Triac Treatment Response to Thyroid Hormone Resistantance

    ESPE Abstracts, 2018

    Source : OpenAlex

  21. Somatostatin Experiment in Prohormone Convertase Deficiency

    57th Annual ESPE, 2018

    Source : OpenAlex

  22. Arthrogryposis Multiplex Congenita Type II and Panhypopituitarism

    ESPE Abstracts, 2018

    Source : OpenAlex

  23. Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus

    Journal of Clinical Research in Pediatric Endocrinology, 2017

    DOI 10.4274/jcrpe.3818 PMID 28720552 6 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  24. Retinal Neural and Vascular Structure in Isolated Growth Hormone Deficiency Children and Evaluation of Growth Hormone Treatment Effect

    Journal of Clinical Research in Pediatric Endocrinology, 2017

    DOI 10.4274/jcrpe.4758 PMID 29082892 7 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  25. Aldosterone synthase deficiency:a new mutation

    Dspace Repository (Marmara Üniversitesi), 2017

    Texte intégral en libre accèsSource : OpenAlex

  26. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

    American Journal of Medical Genetics Part A, 2016

    DOI 10.1002/ajmg.a.37498 PMID 26788866 8 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  27. First report on the nationwide incidence and prevalence of Type 1 diabetes among children in Turkey

    Diabetic Medicine, 2016

    DOI 10.1111/dme.13063 PMID 26814362 39 citations (Europe PMC) Source : OpenAlex

  28. Soluble Endoglin Level Increase Occurs Prior to Development of Subclinical Structural Vascular Alterations in Diabetic Adolescents

    Journal of Clinical Research in Pediatric Endocrinology, 2016

    DOI 10.4274/jcrpe.2906 PMID 27097763 16 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  29. Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

    Journal of Clinical Research in Pediatric Endocrinology, 2016

    DOI 10.4274/jcrpe.3167 PMID 27611604 8 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  30. Endoglin and obestatin levels, cardiometabolic risk factors and subclinical atherosclerosis in children aged 10–18 years

    Journal of Pediatric Endocrinology and Metabolism, 2016

    DOI 10.1515/jpem-2016-0024 PMID 27682709 4 citations (Europe PMC) Source : OpenAlex

  31. Vitamin D Insufficiency is Related to Premature Adrenarche

    55th Annual ESPE, 2016

    Source : OpenAlex

  32. Çocukluk Çağında Tiroid Nodülünde Önemi Belirsiz Atipi

    Turkiye Klinikleri Journal of Case Reports, 2016

    Source : OpenAlex

  33. Early Puberty; Diagnosis, Treatment and Prognosis

    55th ESPE Meeting, 2016

    Source : OpenAlex

  34. Postoperative Water and Electrolyte Disorders and Affecting Factors in Children with Intracranial Tumors

    55th Annual ESPE, 2016

    Source : OpenAlex

  35. 17 Alpha Hydroxylase, 17-20 Lyase Deficiency, a Case with Hypocalcemic Symptoms

    55th Annual ESPE, 2016

    Source : OpenAlex

  36. Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus

    55th Annual ESPE, 2016

    Source : OpenAlex

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

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.1771 PMID 25800473 44 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

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

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.2023 PMID 26831551 7 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  39. Turner Sendromlu Türk Kızlarının Büyüme Eğrileri: FAVOR Turner Sendromu Çalışma Grubu

    Çanakkale Onsekiz Mart University AVESIS, 2015

    Source : OpenAlex

  40. Turner Sendromlu Türk Kızlarının Büyüme Eğrileri:

    Çanakkale Onsekiz Mart University AVESIS, 2015

    Source : OpenAlex

  41. Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.2022 PMID 26777047 8 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  42. Assessment of bone turnover markers and bone mineral density in normal short boys

    Journal of Pediatric Endocrinology and Metabolism, 2015

    DOI 10.1515/jpem-2014-0099 PMID 26197459 5 citations (Europe PMC) Source : OpenAlex

  43. Obezitenin Diğer Komplikasyonları

    Turkiye Klinikleri Pediatric Sciences - Special Topics, 2015

    Source : OpenAlex

  44. Stevens Johnson Syndrome in a Case with Type 1 Diabetes Mellitus: Relation or Coincidence?

    54th ESPE Meeting (ESPE 2015), 2015

    Source : OpenAlex

  45. A Rare Adverse Effect of Methimazole: Serum Sickness

    54th ESPE Meeting (ESPE 2015), 2015

    Source : OpenAlex

  46. First Report of Nationwide Incidence and Prevalence of Type 1 Diabetes Among Children in Turkey

    54th ESPE Meeting (ESPE 2015), 2015

    Source : OpenAlex

  47. Turner Sendromlu Çocukların Başvuru Özellikleri ve Eşlik Eden Patolojiler: 842 Vakanın Ulusal Veritabanında Değerlendirme Sonuçları

    AYBU AVESIS, 2014

    Source : OpenAlex

  48. Nationwide Study of Turner Syndrome During Childhood in Turkey: Evaluation of Associated Problems

    ESPE 2014, 2014

    Source : OpenAlex

  49. Cardio-Facio-Cutaneous Syndrome with Precocious Puberty, Growth Hormone Deficiency and Hyperprolactinemia

    Journal of Clinical Research in Pediatric Endocrinology, 2014

    DOI 10.4274/jcrpe.1151 PMID 24637312 11 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  50. Extensive Middle Cranial Fossa Arachnoid Cysts and Different Clinical Presentation in Two Patients

    Journal of Clinical Research in Pediatric Endocrinology, 2014

    DOI 10.4274/jcrpe.1381 PMID 25241612 2 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex