Wissenschaftliche Arbeiten

Doç. Dr. Bahar Özcabı

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

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  1. Current Practices in Hashimoto's Thyroiditis: Differences in Attitudes Between Pediatric and Adult Endocrinologists in Türkiye: A National Survey

    Journal of Clinical Research in Pediatric Endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2025.2024-9-12 PMID 39849667 Frei zugänglicher VolltextQuelle: OpenAlex

  2. Attitudes Towards the Management of Congenital Hypothyroidism in Türkiye: National Survey Study

    Journal of Clinical Research in Pediatric Endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2025.2024-9-18 PMID 39885770 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  3. A Rare Case of Monogenic Obesity Due to a Novel Variant in the <i>ADCY3</i> Gene: Challenges in Follow-up and Treatment

    Journal of clinical research in pediatric endocrinology, 2025

    DOI 10.4274/jcrpe.galenos.2023.2023-7-2 PMID 37855273 4 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  4. Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study

    Journal of pediatric endocrinology & metabolism : JPEM, 2025

    DOI 10.1515/jpem-2024-0587 PMID 40440520 Quelle: Europe PMC

  5. Semaglutide as a potential treatment for a child with ADCY3 mutation

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.110.ep881 1 Zitation (OpenAlex) Quelle: OpenAlex

  6. Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study

    Journal of clinical research in pediatric endocrinology, 2024

    DOI 10.4274/jcrpe.galenos.2024.2024-1-3 PMID 38664994 10 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  7. Severe adrenal insufficiency in six neonates with normal newborn screening for CAH

    Clinical endocrinology, 2024

    DOI 10.1111/cen.15080 PMID 38796770 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  8. Cinsiyet Gelişim Bozuklukları

    2024

    DOI 10.5152/6800 Quelle: OpenAlex

  9. Cinsel Gelişim Bozukluklarında Tanı

    2024

    DOI 10.5152/6805 Quelle: OpenAlex

  10. The association between vitamin B12, folate, homocysteine levels, and carotid intima-media thickness in children with obesity: a cross-sectional study

    Journal of pediatric endocrinology & metabolism : JPEM, 2022

    DOI 10.1515/jpem-2022-0250 PMID 35822708 Frei zugänglicher VolltextQuelle: Europe PMC

  11. Evaluation of the impact of childhood obesity on retrobulbar hemodynamics and retinal microvasculature

    European Journal of Ophthalmology, 2022

    DOI 10.1177/11206721221086244 PMID 35243922 9 Zitationen (OpenAlex) Quelle: OpenAlex

  12. 46,XY Cinsel Gelişim Bozukluğunda 17-beta hidroksisteroid dehidrojenaz Tip 3

    AYBU AVESIS, 2022

    Quelle: OpenAlex

  13. Evaluation of Thyroid Nodules in Children and Adolescents: Multicenter Study in Turkey

    Güncel Pediatri, 2021

    DOI 10.4274/jcp.2021.43926 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  14. Hypogonadism: Is It Always Hypogonadotropic in an Adolescent With a Cleft Palate? A Surprising Case of Klinefelter Syndrome

    The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2021

    DOI 10.1177/1055665620967601 PMID 33107323 Quelle: Europe PMC

  15. Is Waist-height Ratio Associated with Thyroid Antibody Levels in Children with Obesity?

    Journal of clinical research in pediatric endocrinology, 2021

    DOI 10.4274/jcrpe.galenos.2020.2020.0170 PMID 33006550 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  16. Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2

    Journal of clinical research in pediatric endocrinology, 2021

    DOI 10.4274/jcrpe.galenos.2020.2019.0216 PMID 32539318 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  17. Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

    Journal of clinical research in pediatric endocrinology, 2021

    DOI 10.4274/jcrpe.galenos.2021.2020.0228 PMID 33565750 11 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  18. Evaluation of clinical, endocrine and metabolic findings in obese children with and without hepatosteatosis

    Journal of Pediatric Endocrinology and Metabolism, 2021

    DOI 10.1515/jpem-2021-0034 PMID 34142516 9 Zitationen (Europe PMC) Quelle: ORCID

  19. Management of rapidly progressive precocious puberty in a patient with mosaic turner syndrome

    Acta Endocrinologica, 2021

    DOI 10.4183/aeb.2021.101 PMID 34539916 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  20. Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

    Genetics in Medicine, 2021

    DOI 10.1038/s41436-020-01087-5 PMID 33495532 28 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  21. Associations of Respiratory Distress Syndrome Severity and Other Factors With Transient Hypothyroxinemia of Prematurity

    Cureus, 2021

    DOI 10.7759/cureus.17159 PMID 34548973 9 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  22. A Case of Sotos Syndrome Caused by a Novel Variant in the NSD1 Gene: A Proposed Rationale to Treat Accompanying Precocious Puberty

    Acta Endocrinologica (Bucharest), 2020

    DOI 10.4183/aeb.2020.245 PMID 33029244 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  23. The Relationship Between Obesity, Depressive Symptoms and Sleep Duration in Children and Adolescents

    Acta Medica Alanya, 2020

    DOI 10.30565/medalanya.784624 Frei zugänglicher VolltextQuelle: OpenAlex

  24. Lipid accumulation product is a predictor of nonalcoholic fatty liver disease in childhood obesity

    Korean Journal of Pediatrics, 2019

    DOI 10.3345/kjp.2019.00248 PMID 31870087 25 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  25. Ergen kızlarda polikistik over sendromu: klinik, endokrin ve metabolik bulgular

    Zeynep Kamil Tıp Bülteni, 2019

    DOI 10.16948/zktipb.499708 Quelle: OpenAlex

  26. Waist Circumference Triglyceride Index is Useful to Predict Non-alcoholic Fatty Liver Disease in Childhood Obesity

    58th Annual ESPE Meeting (ESPE 2019), 2019

    Quelle: OpenAlex

  27. Clinical Characteristics and Response to Growth Hormone Treatment in Patients with Prader-Willi Syndrome

    DSpace - Düzce (Duzce University), 2019

    Quelle: OpenAlex

  28. Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

    Journal of Clinical Research in Pediatric Endocrinology, 2018

    DOI 10.4274/jcrpe.0210 PMID 30488822 9 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  29. Tirotoksikozlu Çocuk ve Adolesanların Klinik Özellikleri - Çok Merkezli Bir Çalışma

    AYBU AVESIS, 2018

    Quelle: OpenAlex

  30. Tirotoksikozlu Çocuk ve Adolesanların Klinik Özellikleri - Çok Merkezli Bir Calışma

    AYBU AVESIS, 2018

    Quelle: OpenAlex

  31. 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

  32. Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2018

    DOI 10.4274/jcrpe.5162 PMID 28943513 18 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  33. Effective sociodemographic and clinical factors in weight loss in childhood obesity

    Türk Pediatri Arşivi, 2018

    DOI 10.5152/turkpediatriars.2018.6210 PMID 30459516 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  34. Lipid Accumulation Product is a Predictor of Non-alcoholic Fatty Liver Disease in Childhood Obesity

    57th Annual ESPE, 2018

    1 Zitation (OpenAlex) Quelle: OpenAlex

  35. Astımlı ve sağlıklı çocuklar arasında Helicobacter Pylori sıklığının karşılaştırılması

    Zeynep Kamil Tıp Bülteni, 2018

    DOI 10.16948/zktipb.384311 Quelle: OpenAlex

  36. Lipid Accumulation Product Is a Predictor of Non-alcoholic Fatty Liver Disease in Childhood Obesity

    AYBU AVESIS, 2018

    Quelle: OpenAlex

  37. General health status and intelligence scores of children of mothers with acromegaly do not differ from those of healthy mothers

    Pituitary, 2016

    DOI 10.1007/s11102-016-0717-2 PMID 27033692 15 Zitationen (OpenAlex) Quelle: OpenAlex

  38. A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population

    Journal of Clinical Research in Pediatric Endocrinology, 2016

    DOI 10.4274/jcrpe.3128 PMID 27353739 13 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  39. Apparent diffusion coefficient measurement of ovarian stroma: A potential tool for the diagnosis of polycystic ovary syndrome

    Diagnostic and Interventional Imaging, 2016

    DOI 10.1016/j.diii.2016.09.004 PMID 27773641 7 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  40. Two neonatal diabetes cases with different mutations and treatments

    Endocrine Abstracts, 2016

    DOI 10.1530/endoabs.41.ep408 Frei zugänglicher VolltextQuelle: OpenAlex

  41. Vitamin D Deficiency and Hashimoto’s Thyroiditis in Children and Adolescents: a Critical Vitamin D Level for This Association?

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.2011 PMID 26316435 51 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  42. Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.2067 PMID 26831561 24 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  43. Three Siblings with Corticosterone Methyloxidase Deficiency Type 2 due to c.1175T[gt]C Mutation +a Novel c.788T[gt]A Mutation in CYP11B2 Gene

    54th ESPE Meeting (ESPE 2015), 2015

    Quelle: OpenAlex

  44. Do IGF1 Generation Test Results Predict 1st-Year Growth Response to GH Treatment in Idiopathic Short Stature?

    54th Annual ESPE, 2015

    Quelle: OpenAlex

  45. Timing of precocious pubarche in girls: Does a contemporary subgroup exist?

    ESPE 2014, 2014

    Quelle: OpenAlex

  46. A Case of Vitamin D Dependent Rickets Type 1 with a Novel Mutation in CYP27B1 (25-OH Vitamin D-1-[alpha]-Hydroxylase) Gene

    53rd ESPE Meeting, 2014

    Quelle: OpenAlex

  47. Thyroid Nodules in Childhood and Adolescence; Clinical, Radiologic and Etiological Evaluation

    ESPE 2014, 2014

    Quelle: OpenAlex

  48. On dört yaşında akut lenfoblastik lösemili hastada düzelmeyen taşikardi

    Türk Pediatri Arşivi, 2013

    DOI 10.4274/tpa.665 Frei zugänglicher VolltextQuelle: OpenAlex

  49. Çift görme konuşma bozukluğu halsizlik kol ve bacaklarda güçsüzlük yakınmalarıyla başvuran dokuz yaşında erkek hasta Ayın Olgusu

    DergiPark (Istanbul University), 2009

    DOI 10.4274/tpa.v44i4.5000002180 Quelle: OpenAlex