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List of works by Korcan Demir

A 2-year-old boy with a testicular mass. Diagnosis: testicular tumor of adrenogenital syndrome due to 11-beta-hydroxylase deficiency

scientific article published on August 2010

A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans

scientific article

A comparison of multiple daily insulin therapy with continuous subcutaneous insulin infusion therapy in adolescents with type 1 diabetes mellitus: a single-center experience from Turkey

scientific article published in June 2009

A non-endocrine cause of testicular enlargement mimicking precocious puberty: testicular microlithiasis

scientific article

A nonsense variant in FGFR1: a rare cause of combined pituitary hormone deficiency

scientific article published on 27 August 2020

A novel mutation in the AVPR2 gene (222delA) associated with X-linked nephrogenic diabetes insipidus in a boy with growth failure

scientific article published in March 2010

A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.

scientific article

A toddler with a novel LEPR mutation

scientific article published on 18 February 2019

Acceleration of puberty during growth hormone therapy in a child with septo-optic dysplasia.

scientific article

Anemia in Patients With Resistance to Thyroid Hormone α: A Role for Thyroid Hormone Receptor α in Human Erythropoiesis.

scientific article published in September 2017

Anti-cyclic citrullinated peptide antibodies are not frequently observed in children with type 1 diabetes mellitus: a single-center study.

scientific article published in January 2016

Association of Wolfram syndrome with Fallot tetralogy in a girl

scientific article published in June 2016

Changes of thyroid hormonal status in patients receiving ketogenic diet due to intractable epilepsy.

scientific article published on 11 January 2017

Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study

scientific article published on 04 July 2019

Clarithromycin, montelukast, and pentoxifylline combination treatment ameliorates experimental neonatal hyperoxic lung injury

scientific article published in June 2008

Clinical Heterogeneity and Phenotypic Expansion of NaPi-IIa-Associated Disease

scientific article

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3.

scientific article published on 5 March 2018

Clinical profile and etiologies of children with central diabetes insipidus: a single-center experience from Turkey ⬇️

scientific article published on January 1, 2012

Comparison of Treatment Regimens for the Management of Severe Hypercalcemia due to Vitamin D Intoxication in Children

scientific article published on 05 November 2018

Comparison of the effects of the L-dopa and insulin tolerance tests on cortisol secretion.

scientific article published on 20 January 2018

Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide.

scientific article

Concurrent protracted febrile myalgia syndrome in a child with diabetic ketoacidosis ⬇️

scientific article published on April 5, 2012

Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey

scientific article published on March 2015

Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

scientific article published on 4 May 2016

Fine-needle aspiration biopsy in the diagnosis and follow-up of thyroid nodules in childhood ⬇️

scientific article published on May 5, 2010

GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents.

scientific article

Genetic Causes of Rickets.

scientific article published on 27 December 2017

Graves' disease following allogenic hematopoietic stem cell transplantation for severe aplastic anemia: case report and literature review

scientific article published on 01 April 2018

Growth of Children with Type 1 Diabetes Mellitus ⬇️

scientific article published on May 4, 2010

Higher-Than-Conventional Subcutaneous Regular Insulin Doses in Diabetic Ketoacidosis in Children and Adolescents.

scientific article

Identification of an AR mutation in Klinefelter syndrome during evaluation for penoscrotal hypospadias.

scientific article published in July 2017

Importance of insulin immunoassays in the diagnosis of factitious hypoglycemia

scientific article

Increased circulating interleukin-8 in patients with resistance to thyroid hormone receptor α.

scientific article published in November 2017

Increased concentrations of serum nesfatin-1 levels in childhood with idiopathic chronic malnutrition

scientific article published on 30 April 2018

Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report.

scientific article published in June 2017

Long-term monitoring of Graves’ disease in children and adolescents: a single-center experience

scientific article published on 18 April 2019

Management of central diabetes insipidus with oral desmopressin lyophilisate in infants.

scientific article

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents.

scientific article published on 20 February 2017

Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing.

scientific article

NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATION

scientific article published on 26 September 2019

Neonatal effects of thyroid diseases in pregnancy and approach to the infant with increased TSH: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report.

scientific article

Neurodevelopmental Outcome of Children with Congenital Hypothyroidism Diagnosed in a National Screening Program in Turkey.

scientific article published on 29 March 2017

Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A.

scientific article published on July 2015

Positive correlation of galanin with insulin resistance and triglyceride levels in obese children

scientific article published on 14 June 2018

Presentation of central precocious puberty in two patients with Tay-Sachs disease

scientific article published on 25 June 2018

Psychomotor retardation caused by a defective thyroid hormone transporter: report of two families with different MCT8 mutations

scientific article published on 18 September 2014

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

scientific article

Relationship between oxidative stress and blood glucose fluctuations evaluated with daily glucose monitoring in children with type 1 diabetes mellitus

scientific article published on 14 January 2016

Serum Level of Biotin Rather than the Daily Dosage Is the Main Determinant of Interference on Thyroid Function Assays

scientific article published on 25 October 2019

Serum galectin-1 levels are positively correlated with body fat and negatively with fasting glucose in obese children

scientific article published on 17 July 2017

TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis ⬇️

scientific article published on January 1, 2012

Tamoxifen as First-line Treatment in a Premenarchal Girl with Juvenile Breast Hypertrophy ⬇️

scientific article published on October 1, 2010

The Missense Alteration A5T of the Thyroid Peroxidase Gene is Pathogenic and Associated with Mild Congenital Hypothyroidism

scientific article published on September 2015

The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study

scientific article published on 23 March 2012

Turning over a new page in the national neonatal endocrinological approach

scientific article published on 25 December 2018

Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency

scientific article published in July 2015

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