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List of works by Eda Mengen

A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.

scientific article published in May 2018

A Rare Etiology of 46, XY Disorder of Sex Development and Adrenal Insufficiency: A case of MIRAGE syndrome caused by mutations in SAMD9 gene

scientific article published on 18 June 2019

A duplication upstream of SOX9 associated with SRY negative 46,XX ovotesticular disorder of sex development: A case report

scientific article published on 03 September 2019

CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration

scientific article published on 25 March 2016

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

scientific article published on 23 January 2017

Catecholamine-Induced Myocarditis in a Child with Pheochromocytoma

scientific article published on 18 June 2019

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

scientific article published on 5 November 2018

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

scientific article

Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism

scientific article

Dynamic Thiol/Disulphide Homeostasis in Children and Adolescents with Non-Autoimmune Subclinical Hypothyroidism.

scientific article published on 25 January 2018

Ecthyma gangrenosum in a previously healthy pediatric patient and associated facial paralysis and persistent hyperplastic primary vitreous.

scientific article published on 15 October 2012

Effects of methylphenidate on appetite and growth in children diagnosed with attention deficit and hyperactivity disorder.

scientific article published on 15 August 2015

Enzyme Replacement Therapy in Hypophosphatasia

scientific article published on 01 September 2018

Evaluation of the relationship between short-term glycemic control and netrin-1, a urinary proximal tubular injury marker in children with type 1 diabetes

scientific article published on 01 August 2019

Evaluation of the relationship between the one-hour plasma glucose concentration and beta-cell functions and cardiometabolic parameters during oral glucose tolerance test in obese children and adolescents

scientific article published on 24 May 2020

Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

scientific article published on 21 August 2018

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

scientific article

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1. ⬇️

scientific article published on 18 April 2016

Loss-of-function mutations in PNPLA6 encoding neuropathy target esterase underlie pubertal failure and neurological deficits in Gordon Holmes syndrome

scientific article

Mutations in FEZF1 cause Kallmann syndrome

scientific article

Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families.

scientific article published on 7 November 2014

Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism

scientific article published on 26 December 2018

Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty

scientific article published on 20 January 2018

Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto’s Thyroiditis

scientific article published on 20 June 2019

The Significance of Thiol/Disulfide Homeostasis and Ischemia-modified Albumin Levels in Assessing Oxidative Stress in Obese Children and Adolescents

scientific article published on 15 August 2019

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