Scientific work

Prof. Dr. Heves Kırmızıbekmez

81 publications. The source of the information is stated next to each publication.

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  1. Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn

    The Turkish Journal of Pediatrics, 2017

    DOI 10.24953/turkjped.2017.01.020 PMID 29168375 Open-access full textSource: OpenAlex

  2. Ocular Surface Characteristics in Diabetic Children

    Current Eye Research, 2016

    DOI 10.3109/02713683.2015.1136421 PMID 27159168 41 citations (OpenAlex) Source: OpenAlex

  3. A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

    Journal of Clinical Research in Pediatric Endocrinology, 2016

    DOI 10.4274/jcrpe.2717 PMID 27087618 27 citations (OpenAlex) Open-access full textSource: OpenAlex

  4. Bilateral Complete Epididymal-Testicular Fusion Defects in Case with Partial Androgen Insensitivity: Case Report

    Turkiye Klinikleri Journal of Case Reports, 2016

    DOI 10.5336/caserep.2014-42908 Open-access full textSource: OpenAlex

  5. Çocuk ve Adölesanlarda Obezite ve Beslenme Durumu ile Böbrek ve Karaciğer Fonksiyonları Arasındaki İlişkinin Belirlenmesi

    DergiPark (Istanbul University), 2016

    Source: OpenAlex

  6. Determining the Relationship between Obesity and Nutritional Statusand Renal and Hepatic Functions in Children and Adolescents

    İzmir Katip Celebi University, 2016

    Open-access full textSource: OpenAlex

  7. A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor

    Case Reports in Pediatrics, 2015

    DOI 10.1155/2015/439239 PMID 26366315 9 citations (OpenAlex) Open-access full textSource: OpenAlex

  8. Autoimmune Polyglandular Syndrome Type 2: A Rare Condition in Childhood

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.1394 PMID 25800482 24 citations (OpenAlex) Open-access full textSource: OpenAlex

  9. A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.2249 PMID 26777049 17 citations (OpenAlex) Open-access full textSource: OpenAlex

  10. Tamoxifen-associated hirsutism: an unusual side effect in a 5-year-old girl with McCune-Albright syndrome

    Journal of Pediatric Endocrinology and Metabolism, 2015

    DOI 10.1515/jpem-2014-0437 PMID 26024247 1 citation (OpenAlex) Source: OpenAlex

  11. Effects of Nutrition and Vitamin D Deficiency on Central Puberty Precocious

    54th ESPE Meeting (ESPE 2015), 2015

    1 citation (OpenAlex) Source: OpenAlex

  12. Concurrence of Meningomyelocele and Salt-Wasting Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

    Case Reports in Pediatrics, 2015

    DOI 10.1155/2015/196374 PMID 25685584 Open-access full textSource: OpenAlex

  13. Two Patients with Allen-Herndon-Dudley Syndrome: a Novel Mutation on MCT8 Gene

    54th ESPE Meeting (ESPE 2015), 2015

    Source: OpenAlex

  14. Clinical Features and Pubertal Timing in Girls with Premature Adrenarche

    54th Annual ESPE, 2015

    Source: OpenAlex

  15. GH and Prolactin Secreting Adenoma in an Adolescent Boy

    54th Annual ESPE, 2015

    Source: OpenAlex

  16. Laron Syndrome Caused by a Large Deletion in GH Receptor Gene

    54th ESPE Meeting (ESPE 2015), 2015

    Source: OpenAlex

  17. A case of osteogenesis imperfecta mimicking the features of mucopolysaccharidosis IVA

    Bone Abstracts, 2015

    DOI 10.1530/boneabs.4.p121 Source: OpenAlex

  18. Clinical Effects of Vitamin D in Children with Asthma

    International Archives of Allergy and Immunology, 2014

    DOI 10.1159/000366279 PMID 25277142 51 citations (OpenAlex) Source: OpenAlex

  19. Astımda Kontrolü Zorlaştıran Ender Bir Durum: Vokal Kord Disfonksiyonu

    Çocuk Dergisi / Journal of Child, 2014

    DOI 10.5222/j.child.2013.119 Open-access full textSource: OpenAlex

  20. Metabolic Bone Disease of Prematurity: Report of Four Cases

    Journal of Clinical Research in Pediatric Endocrinology, 2014

    DOI 10.4274/jcrpe.1282 PMID 24932605 20 citations (OpenAlex) Open-access full textSource: OpenAlex

  21. Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report

    Journal of Pediatric Endocrinology and Metabolism, 2014

    DOI 10.1515/jpem-2014-0071 PMID 25153220 11 citations (OpenAlex) Source: OpenAlex

  22. Atypical Presentation of Hashimoto’s Disease in an Adolescent: Thyroid-Associated Ophthalmopathy

    Journal of Clinical Research in Pediatric Endocrinology, 2014

    DOI 10.4274/jcrpe.1450 PMID 25541900 10 citations (OpenAlex) Open-access full textSource: OpenAlex

  23. Erythrocyte Sedimentation Rate and CRP Levels in Childhood Obesity

    ESPE 2014, 2014

    Source: OpenAlex

  24. Clinical Effects of Vitamin D in Asthma

    ESPE 2014, 2014

    Source: OpenAlex

  25. Three Siblings with Gonadal Dysgenesis

    53rd ESPE Meeting, 2014

    Source: OpenAlex

  26. Multiple Endocrinopathies in a Case with H Syndrome due to a Novel slc29a3 Mutation

    53rd ESPE Meeting, 2014

    Source: OpenAlex

  27. Tamoxifen-Induced Hirsutism: an Unusual Side Effect in a 5 Years Old Girl with Mccune-Albright Syndrome

    ESPE 2014, 2014

    Source: OpenAlex

  28. Detection of vascular risk markers in children and adolescents with type 1 diabetes

    Journal of Pediatric Endocrinology and Metabolism, 2013

    DOI 10.1515/jpem-2013-0046 PMID 23945124 2 citations (OpenAlex) Source: OpenAlex

  29. Developmental Defects of the Thyroid Gland: Relationship with Advanced Maternal Age

    Journal of Clinical Research in Pediatric Endocrinology, 2012

    DOI 10.4274/jcrpe.560 PMID 22672863 21 citations (OpenAlex) Open-access full textSource: OpenAlex

  30. Clinical features and management of diabetic ketoacidosis in different age groups of children: children less than 5 years of age are at higher risk of metabolic decompensation

    Journal of Pediatric Endocrinology and Metabolism, 2012

    DOI 10.1515/jpem-2012-0110 PMID 23426821 6 citations (OpenAlex) Source: OpenAlex

  31. Multiple pterygium syndrome: mimicking the findings of Turner syndrome

    Journal of Pediatric Endocrinology and Metabolism, 2011

    DOI 10.1515/jpem.2011.367 PMID 22308873 3 citations (OpenAlex) Source: OpenAlex