Prof. Dr. Heves Kırmızıbekmez

Cholestasis and hypercalcemia secondary to panhypopituitarism in a newborn

The Turkish Journal of Pediatrics, 2017

DOI 10.24953/turkjped.2017.01.020 PMID 29168375 Frei zugänglicher VolltextQuelle: OpenAlex

Ocular Surface Characteristics in Diabetic Children

Current Eye Research, 2016

DOI 10.3109/02713683.2015.1136421 PMID 27159168 41 Zitationen (OpenAlex) Quelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Frei zugänglicher VolltextQuelle: OpenAlex

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

DergiPark (Istanbul University), 2016

Quelle: OpenAlex

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

İzmir Katip Celebi University, 2016

Frei zugänglicher VolltextQuelle: OpenAlex

A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor

Case Reports in Pediatrics, 2015

DOI 10.1155/2015/439239 PMID 26366315 9 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitation (OpenAlex) Quelle: OpenAlex

Effects of Nutrition and Vitamin D Deficiency on Central Puberty Precocious

54th ESPE Meeting (ESPE 2015), 2015

1 Zitation (OpenAlex) Quelle: OpenAlex

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 Frei zugänglicher VolltextQuelle: OpenAlex

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

54th ESPE Meeting (ESPE 2015), 2015

Quelle: OpenAlex

Clinical Features and Pubertal Timing in Girls with Premature Adrenarche

54th Annual ESPE, 2015

Quelle: OpenAlex

GH and Prolactin Secreting Adenoma in an Adolescent Boy

54th Annual ESPE, 2015

Quelle: OpenAlex

Laron Syndrome Caused by a Large Deletion in GH Receptor Gene

54th ESPE Meeting (ESPE 2015), 2015

Quelle: OpenAlex

A case of osteogenesis imperfecta mimicking the features of mucopolysaccharidosis IVA

Bone Abstracts, 2015

DOI 10.1530/boneabs.4.p121 Quelle: OpenAlex

Clinical Effects of Vitamin D in Children with Asthma

International Archives of Allergy and Immunology, 2014

DOI 10.1159/000366279 PMID 25277142 51 Zitationen (OpenAlex) Quelle: OpenAlex

Astımda Kontrolü Zorlaştıran Ender Bir Durum: Vokal Kord Disfonksiyonu

Çocuk Dergisi / Journal of Child, 2014

DOI 10.5222/j.child.2013.119 Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitationen (OpenAlex) Quelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Erythrocyte Sedimentation Rate and CRP Levels in Childhood Obesity

ESPE 2014, 2014

Quelle: OpenAlex

Clinical Effects of Vitamin D in Asthma

ESPE 2014, 2014

Quelle: OpenAlex

Three Siblings with Gonadal Dysgenesis

53rd ESPE Meeting, 2014

Quelle: OpenAlex

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

53rd ESPE Meeting, 2014

Quelle: OpenAlex

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

ESPE 2014, 2014

Quelle: OpenAlex

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 Zitationen (OpenAlex) Quelle: OpenAlex

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 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

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 Zitationen (OpenAlex) Quelle: OpenAlex

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 Zitationen (OpenAlex) Quelle: OpenAlex