Wissenschaftliche Arbeiten

Prof. Dr. Teoman Akçay

103 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  1. Early dynamic glucose dysregulation in obese adolescents with obstructive sleep apnea: a comparative analysis with fasting lactate

    Journal of Endocrinological Investigation, 2026

    DOI 10.1007/s40618-026-02999-w PMID 42545670 Quelle: ORCID

  2. Shunt Revision Frequency Is Associated with Motor Function and Anthropometric Growth in Pediatric Hydrocephalus

    Research Square, 2026

    DOI 10.21203/rs.3.rs-10156489/v1 Frei zugänglicher VolltextQuelle: OpenAlex

  3. Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNA

    EBioMedicine, 2026

    DOI 10.1016/j.ebiom.2026.106308 PMID 42184599 Frei zugänglicher VolltextQuelle: OpenAlex

  4. Obezite 1

    Ataturk University - AVESIS, 2025

    Quelle: OpenAlex

  5. Oyun bağımlılığı ve hipertansiyon: Güncel bir inceleme

    Istanbul Health and Technology University Institutional Repository, 2025

    Frei zugänglicher VolltextQuelle: OpenAlex

  6. Akdeniz diyeti: Sağlıklı yaşamın sırrı

    Istanbul Health and Technology University Institutional Repository, 2025

    Quelle: OpenAlex

  7. Fruktoz: Dost mu düşman mı?

    Istanbul Health and Technology University Institutional Repository, 2025

    Frei zugänglicher VolltextQuelle: OpenAlex

  8. 6687 New indication for monogenic diabetes genetic testing in children – implication for routine clinical practice

    British Society for Paediatric Endocrinology and Diabetes Meeting (BSPED), 2024

    DOI 10.1136/archdischild-2024-rcpch.361 Quelle: OpenAlex

  9. A homozygous TARS2 variant is a novel cause of syndromic neonatal diabetes

    Diabetic Medicine, 2024

    DOI 10.1111/dme.15471 PMID 39509107 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  10. Pediatric Pathological Fractures

    2023

    DOI 10.69860/nobel.9786053359036 Quelle: ORCID

  11. Late-effects of Chemoradiotherapy on Growth and Puberty in Survivors of Childhood Acute Lymphoblastic Leukemia

    Trends in Pediatrics, 2022

    DOI 10.4274/tp.2022.43043 Frei zugänglicher VolltextQuelle: ORCID

  12. Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

    Diabetologia, 2021

    DOI 10.1007/s00125-021-05597-y PMID 34686905 20 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  13. Pediatricians’ COVID-19 experiences and views on the willingness to receive COVID-19 vaccines: a cross-sectional survey in Turkey

    Human Vaccines and Immunotherapeutics, 2021

    DOI 10.1080/21645515.2021.1896319 PMID 33861165 25 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  14. Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases

    The Journal of Clinical Endocrinology & Metabolism, 2020

    DOI 10.1210/clinem/dgaa022 PMID 31950145 20 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  15. Retrospective Analysis of Cases with Premature Thelarche

    Bagcilar Medical Bulletin, 2020

    DOI 10.4274/bmb.galenos.2020.03.08 Frei zugänglicher VolltextQuelle: ORCID

  16. Distribution of α-actinin-3 rs1815739 and angiotensin-1 converting enzyme indel polymorphisms in Turkish bodybuilders

    Biomedical Reports, 2020

    DOI 10.3892/br.2020.1374 PMID 33149911 Frei zugänglicher VolltextQuelle: ORCID

  17. Genetics of Sleep and Sleep Disorders

    Neurological Modulation of Sleep: Mechanisms and Function of Sleep Health, 2020

    DOI 10.1016/b978-0-12-816658-1.00005-3 2 Zitationen (OpenAlex) Quelle: ORCID

  18. Multivitamin with L-Arginine supplementation can increase linear growth velocity in children with idiopathic short stature without affecting bone maturation

    Progress in Nutrition, 2020

    DOI 10.23751/pn.v22i4.10652 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: ORCID

  19. The Use of Social Network in Daily Pediatric Practice and Education: Turkish Pediatric Atelier

    International Journal of Pediatrics (United Kingdom), 2020

    DOI 10.1155/2020/7301309 PMID 33029152 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  20. 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 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  21. Evaluation of Molecular Characteristics and Steroid Metabolomics in a Large Cohort of Children with 3β-Hydroxysteroid Dehydrogenase 2 Deficiency

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  22. Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3 beta-hydroxysteroid dehydrogenase 2 deficiency

    AYBU AVESIS, 2019

    Quelle: OpenAlex

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

    Journal of Clinical Research in Pediatric Endocrinology, 2018

    DOI 10.4274/jcrpe.0025 PMID 29789274 8 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  24. Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology

    Dspace Repository (Marmara Üniversitesi), 2018

    Frei zugänglicher VolltextQuelle: OpenAlex

  25. Comprehensive Genetic Testing Shows One in FiveChildren with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology.

    Kocaeli Üniversitesi - AVESİS, 2018

    Quelle: OpenAlex

  26. -174 G/C polymorphism of interleukin 6 gene is not significantly different in Turkish professional short and long distance runners.

    Cellular and molecular biology (Noisy-le-Grand, France), 2018

    DOI 10.14715/cmb/2018.64.11.15 PMID 30213294 Frei zugänglicher VolltextQuelle: ORCID

  27. Emergence of insulin resistance following empirical glibenclamide therapy: A case report of neonatal diabetes with a recessive INS gene mutation

    Journal of Pediatric Endocrinology and Metabolism, 2018

    DOI 10.1515/jpem-2017-0325 PMID 29305569 6 Zitationen (Europe PMC) Quelle: ORCID

  28. Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism

    EBioMedicine, 2018

    DOI 10.1016/j.ebiom.2018.09.024 PMID 30266295 11 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  29. Frequency of Enzyme Deficiencies in a Turkish Cohort of Congenital Adrenal Hyperplasia: A Single-Center Experience with 145 Patients

    57th Annual ESPE, 2018

    Quelle: OpenAlex

  30. Significance of S100A8, S100A9 and calprotectin levels in bladder cancer

    Scandinavian Journal of Clinical and Laboratory Investigation, 2017

    DOI 10.1080/00365513.2017.1336567 PMID 28609200 32 Zitationen (Europe PMC) Quelle: OpenAlex

  31. Association between endocrine diseases and serous otitis media in children

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2017

    DOI 10.4274/jcrpe.3585 PMID 27612192 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

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

    Dspace Repository (Marmara Üniversitesi), 2016

    Frei zugänglicher VolltextQuelle: OpenAlex

  33. Significance of serum c-erbB-2 oncoprotein, insulin-like growth factor-1 and vascular endothelial growth factor levels in ovarian cancer.

    Bratislavske lekarske listy, 2016

    DOI 10.4149/bll_2016_032 PMID 26925746 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  34. Autosomal-recessive mutations in SLC34A1 encoDing sodium-phosphate cotransporter 2a cause idiopathic infantile hypercalcemia

    Journal of the American Society of Nephrology, 2016

    DOI 10.1681/asn.2014101025 PMID 26047794 185 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  35. Misunderstood about obesity, sleep apnea and metabolic syndrome in adolescents

    Journal of Clinical Sleep Medicine, 2016

    DOI 10.5664/jcsm.5914 PMID 27092705 Frei zugänglicher VolltextQuelle: ORCID

  36. Clinical and Molecular Characteristics of Turkish Patients with Congenital Hyperinsulinism: A Single-Center Experience

    Dspace Repository (Marmara Üniversitesi), 2016

    Frei zugänglicher VolltextQuelle: OpenAlex

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

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.1794 PMID 25800474 11 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

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

    54th ESPE Meeting (ESPE 2015), 2015

    Quelle: OpenAlex

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

    54th ESPE Meeting (ESPE 2015), 2015

    Quelle: OpenAlex

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

    The Journal of Clinical Endocrinology & Metabolism, 2015

    DOI 10.1210/jc.2015-3250 PMID 26523528 130 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  41. Is Metabolic Syndrome Associated with Obstructive Sleep Apnea in Obese Adolescents?

    Journal of Clinical Sleep Medicine, 2015

    DOI 10.5664/jcsm.5266 PMID 26156956 16 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  42. Expanding the clinical spectrum associated with GLIS3 mutations

    Journal of Clinical Endocrinology and Metabolism, 2015

    DOI 10.1210/jc.2015-1827 PMID 26259131 58 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  43. Distribution of Mutations in Genes Known to be Associated with Familial Idiopathic Hypogonadotropic Hypogonadism in a Large Cohort

    54th Annual ESPE, 2015

    Quelle: OpenAlex

  44. Transient Neonatal Diabetes Mellitus with Maternal Methylation Loss

    The Journal of Pediatric Research, 2015

    DOI 10.4274/jpr.80299 Frei zugänglicher VolltextQuelle: OpenAlex

  45. Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

    Orphanet Journal of Rare Diseases, 2014

    DOI 10.1186/1750-1172-9-60 PMID 24767306 31 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  46. AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity

    Andrology, 2014

    DOI 10.1111/j.2047-2927.2014.00215.x PMID 24737579 43 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  47. Non-alcoholic fatty liver disease in obese children and the relationship between metabolic syndrome criteria

    Obesity Research and Clinical Practice, 2014

    DOI 10.1016/j.orcp.2013.08.003 PMID 25091357 41 Zitationen (Europe PMC) Quelle: ORCID

  48. Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

    Human Molecular Genetics, 2014

    DOI 10.1093/hmg/ddu360 PMID 25015100 47 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  49. The Frequency and the Effects of 21-Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients

    Annals of Human Genetics, 2014

    DOI 10.1111/ahg.12083 PMID 25227725 9 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  50. Pamidronate treatment in patient developed hypercalcemia due to hypervitaminosis D

    SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital, 2014

    DOI 10.5350/semb.20140715062539 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex