Zehra Aycan

Structure of the PAPP-ABP5 complex reveals mechanism of substrate recognition

TFOS DEWS II Diagnostic Methodology report

The Oslo definitions for coeliac disease and related terms

TFOS DEWS II pathophysiology report

2012 European Thyroid Association Guidelines for the Management of Familial and Persistent Sporadic Non-Autoimmune Hyperthyroidism Caused by Thyroid-Stimulating Hormone Receptor Germline Mutations

TFOS DEWS II Epidemiology Report

The multiple-hit pathogenesis of non-alcoholic fatty liver disease (NAFLD)

TFOS DEWS II Definition and Classification Report

Role of ginsenosides, the main active components of Panax ginseng , in inflammatory responses and diseases

TFOS DEWS II Management and Therapy Report

Mammalian NADPH Oxidases

TFOS DEWS II Sex, Gender, and Hormones Report

<p>Reactive Oxygen Species: Drivers of Physiological and Pathological Processes</p>

Nonalcoholic fatty liver disease: A comprehensive review of a growing epidemic

Steroid 5α-reductase 2 deficiency

Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and Postpartum

2017 Guidelines of the American Thyroid Association for the Diagnosis and Management of Thyroid Disease During Pregnancy and the Postpartum

Celiac disease and gluten-associated diseases.

Treatment of central precocious puberty

Congenital rickets.

Oral Bisphosphonate Therapy for Vitamin D Intoxication of the Infant

The Chemistry of Reactive Oxygen Species (ROS) Revisited: Outlining Their Role in Biological Macromolecules (DNA, Lipids and Proteins) and Induced Pathologies

The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders

The Efficacy of Red Ginseng in Type 1 and Type 2 Diabetes in Animals

Non-Classical Congenital Adrenal Hyperplasia in Childhood

Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons: An Endocrine Society* Clinical Practice Guideline

Clinical, Genetic, and Functional Characterization of Adrenocorticotropin Receptor Mutations Using a Novel Receptor Assay

Mutations of the 5α-Steroid Reductase Type 2 Gene in Six Turkish Patients from Unrelated Families and a Large Pedigree of an Isolated Turkish Village

Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene-Case Report

The Relationship Between Pediatric Nonalcoholic Fatty Liver Disease and Cardiovascular Risk Factors and Increased Risk of Atherosclerosis in Obese Children

A novel mutation of 5α-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism

Severe Hypercalcemia of an Infant Due to Vitamin D Toxicity Associated With Hypercholesterolemia

Latent Autoimmune Diabetes Mellitus in Children (LADC) with Autoimmune Thyroiditis and Celiac Disease

Effects on Bone Mineral Density of Gonadotropin Releasing Hormone Analogs Used in the Treatment of Central Precocious Puberty

A girl with steroid cell ovarian tumor misdiagnosed as non-classical congenital adrenal hyperplasia.

Syndrome of Congenital Adrenocortical Unresponsiveness to ACTH. Report of Six Patients

Dry Eye Syndrome in Diabetic Children

Audiologic evaluation in pediatric patients with type 1 diabetes mellitus