Bilimsel çalışmalar
Prof. Dr. Peyami Cinaz
183 yayın. Her yayının yanında bilginin kaynağı yazar.
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Early Cardiometabolic Characteristics in Childhood Among Large-for-Gestational-Age Infants
Pediatric Practice and Research, 2026
DOI 10.21765/pprjournal.1974143 Açık erişimli tam metinKaynak: OpenAlex
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Vitamin D, Insulin Resistance and Cytokine Levels in Obese Pubertal Children
The Journal of Pediatric Academy, 2023
DOI 10.4274/jpea.2023.213 Kaynak: OpenAlex
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Kistik Fibroziste Endokrin Sistem Tutulumu ve Tedavi Yaklaşımları
2021
Kaynak: OpenAlex
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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 atıf (Europe PMC) Kaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Kistik Fibrozis ile İlişkili Diyabet: Bir Olgu Sunumu
Journal of Nutrition and Dietetics, 2020
DOI 10.33076/2020.bdd.1346 Kaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Congenital Generalized Lipodystrophy Type 4 - New Mutation in the CAVIN1 Gene
58th Annual ESPE Meeting (ESPE 2019), 2019
Kaynak: OpenAlex
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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
Kaynak: OpenAlex
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Cinacalcet Experience in Hypercalcemia Due to CaSR Mutation
58th Annual ESPE Meeting (ESPE 2019), 2019
Kaynak: OpenAlex
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A Case of Panhipopituitarism with SOX3 Gene Deletion
58th Annual ESPE Meeting (ESPE 2019), 2019
Kaynak: OpenAlex
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Long-Term Honeymoon Period in Type 1 Diabetes: True Diagnosis MODY5; New Mutation of HNF1B
58th Annual ESPE Meeting (ESPE 2019), 2019
Kaynak: OpenAlex
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Relationship between obesity and iron deficiency anemia: is there a role of hepcidin?
Hematology, 2018
DOI 10.1080/10245332.2018.1423671 PMID 29318945 34 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Kaynak: OpenAlex
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Vitamin D status and premature adrenarche
Pediatrics International, 2018
DOI 10.1111/ped.13682 PMID 30129969 4 atıf (Europe PMC) Kaynak: OpenAlex
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Clinical and Epidemiological Features of Children with Type 1 Diabetes
57th Annual ESPE, 2018
Kaynak: OpenAlex
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The Levels of Blood Glucose and Counting of Carbohydrate-Fat-Protein in Diabetic Children Using Pump with Aspart and Glulisine
57th Annual ESPE, 2018
Kaynak: OpenAlex
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Triac Treatment Response to Thyroid Hormone Resistantance
ESPE Abstracts, 2018
Kaynak: OpenAlex
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Somatostatin Experiment in Prohormone Convertase Deficiency
57th Annual ESPE, 2018
Kaynak: OpenAlex
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Arthrogryposis Multiplex Congenita Type II and Panhypopituitarism
ESPE Abstracts, 2018
Kaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Aldosterone synthase deficiency:a new mutation
Dspace Repository (Marmara Üniversitesi), 2017
Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Kaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Kaynak: OpenAlex
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Vitamin D Insufficiency is Related to Premature Adrenarche
55th Annual ESPE, 2016
Kaynak: OpenAlex
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Çocukluk Çağında Tiroid Nodülünde Önemi Belirsiz Atipi
Turkiye Klinikleri Journal of Case Reports, 2016
Kaynak: OpenAlex
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Early Puberty; Diagnosis, Treatment and Prognosis
55th ESPE Meeting, 2016
Kaynak: OpenAlex
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Postoperative Water and Electrolyte Disorders and Affecting Factors in Children with Intracranial Tumors
55th Annual ESPE, 2016
Kaynak: OpenAlex
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17 Alpha Hydroxylase, 17-20 Lyase Deficiency, a Case with Hypocalcemic Symptoms
55th Annual ESPE, 2016
Kaynak: OpenAlex
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Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus
55th Annual ESPE, 2016
Kaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Turner Sendromlu Türk Kızlarının Büyüme Eğrileri: FAVOR Turner Sendromu Çalışma Grubu
Çanakkale Onsekiz Mart University AVESIS, 2015
Kaynak: OpenAlex
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Turner Sendromlu Türk Kızlarının Büyüme Eğrileri:
Çanakkale Onsekiz Mart University AVESIS, 2015
Kaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Kaynak: OpenAlex
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Obezitenin Diğer Komplikasyonları
Turkiye Klinikleri Pediatric Sciences - Special Topics, 2015
Kaynak: OpenAlex
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Stevens Johnson Syndrome in a Case with Type 1 Diabetes Mellitus: Relation or Coincidence?
54th ESPE Meeting (ESPE 2015), 2015
Kaynak: OpenAlex
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A Rare Adverse Effect of Methimazole: Serum Sickness
54th ESPE Meeting (ESPE 2015), 2015
Kaynak: OpenAlex
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First Report of Nationwide Incidence and Prevalence of Type 1 Diabetes Among Children in Turkey
54th ESPE Meeting (ESPE 2015), 2015
Kaynak: OpenAlex
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Turner Sendromlu Çocukların Başvuru Özellikleri ve Eşlik Eden Patolojiler: 842 Vakanın Ulusal Veritabanında Değerlendirme Sonuçları
AYBU AVESIS, 2014
Kaynak: OpenAlex
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Nationwide Study of Turner Syndrome During Childhood in Turkey: Evaluation of Associated Problems
ESPE 2014, 2014
Kaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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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 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex