E. Mengen

发表

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

S. Ojeda, C. McArdle, B. Hamel, 2014, The Journal of clinical endocrinology and metabolism.

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

B. I. Hutchins, S. Wray, A. Topaloğlu, 2016, Endocrinology.

DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

A. Topaloğlu, L. D. Kotan, E. Mengen, 2021, Hormone Research in Paediatrics.

A novel genetic mutation in a Turkish family with GCK-MODY

E. Mengen, B. Yuksel, S. Ceylaner, 2015, International Journal of Diabetes in Developing Countries.

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

E. Mengen, Ç. Yücel, Selin Elmaoğulları, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

The Relation of Vitamin D Levels to Insulin Resistance and Hepatosteatosis in Obese Children

E. Mengen, Pınar Kocaay, P. Kocaay, 2018, Turkish Journal of Pediatric Disease.

Effects of the information-motivation-behavioral skills model on metabolic control of adolescents with type 1 diabetes in Turkey: Randomized controlled study.

E. Mengen, H. Çavuşoğlu, Elif Bakır, 2020, Journal of pediatric nursing.

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

S. Poyrazoglu, F. Baş, F. Darendeliler, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

B. I. Hutchins, S. Wray, A. Topaloğlu, 2017, The Journal of clinical endocrinology and metabolism.

Investigation of the prevalence of cardiovascular risk factors in obese patients diagnosed with metabolic syndrome in childhood and examination of left ventricular function by echocardiography

M. Kızılgün, E. Mengen, Ahmet Uçaktürk, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Loss-of-Function Mutations in SEMA3F and gePLXNA3 Encoding Semaphorin-3F and its Receptor Plexin-A3 Respectively Cause Idiopathic Hypogonadotropic Hypogonadism

F. Darendeliler, A. Topaloğlu, L. D. Kotan, 2022 .

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

A. Topaloğlu, L. D. Kotan, E. Mengen, 2015, Hormone Research in Paediatrics.

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

A. Topaloğlu, L. D. Kotan, E. Mengen, 2015, Clinical endocrinology.

The Effects of Risk Behaviors and Orthorexic Behavior on Glycemic Control in Adolescents with Type 1 Diabetes

E. Mengen, Demet Taş, S. A. Uçaktürk, 2019, Journal of clinical research in pediatric endocrinology.

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

A. Topaloğlu, L. D. Kotan, E. Mengen, 2018, Clinical genetics.

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

I. Carr, A. Topaloğlu, L. D. Kotan, 2016, Journal of clinical research in pediatric endocrinology.

A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene

E. Mengen, S. A. Uçaktürk, Aynur Küçükçongar Yavaş, 2019, Journal of clinical research in pediatric endocrinology.

Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

F. Darendeliler, A. Topaloğlu, L. D. Kotan, 2021, Genetics in Medicine.

Evaluation of the Children with Hypoparathyroidism and Pseudohypoparathyroidism Presenting to an Endocrinology Outpatient Clinic

E. Mengen, Pınar Kocaay, 2018, Journal of Ankara University Faculty of Medicine.

Enzyme-replacement therapy for hypophosphatasia.

E. Mengen, S. Ünal, Selin Elmaoğulları, 2012, BoneKEy reports.

The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development

J. Grötzinger, A. Topaloğlu, E. Mengen, 2013, Hormone Research in Paediatrics.

Mutations in FEZF1 cause Kallmann syndrome.

B. I. Hutchins, S. Wray, F. Demirel, 2014, American journal of human genetics.

Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

E. Mengen, B. Yüksel, Fatih Gürbüz, 2020, Journal of clinical research in pediatric endocrinology.

The Significance of Thiol / Disulfide Homeostasis and Ischemia-Modified Albumin Levels in Assessing the Oxidative Stress in Obese Children and Adolescents Running Head : Oxidative Stress in Obese Children and Adolescents

E. Mengen, S. Neşelioğlu, Ö. Erel, 2019 .

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

E. Mengen, Aynur Kucukcongar Yavas, 2019, Journal of Clinical Research in Pediatric Endocrinology.

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

E. Mengen, F. Temiz, I. Bucak, 2012, The American journal of case reports.

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

E. Mengen, E. Azak, I. Cetin, 2019, Journal of clinical research in pediatric endocrinology.

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

A. Topaloğlu, L. D. Kotan, E. Mengen, 2017, Journal of clinical research in pediatric endocrinology.

Catecholamine-induced Myocarditis in a Child with Pheochromocytoma

E. Mengen, E. Azak, I. Cetin, 2019, Journal of Clinical Research in Pediatric Endocrinology.

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

E. Mengen, S. A. Uçaktürk, Eda Mengen, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

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

E. Mengen, Ö. Erel, M. Alışık, 2018, Medical Principles and Practice.

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

F. Baş, Z. Aycan, E. Mengen, 2018, Journal of Endocrinological Investigation.

Comparison of Calcitonin and Pamidronate Treatments in Children with Osteogenesis Imperfecta

A. Topaloğlu, E. Mengen, F. Gurbuz, 2013 .

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

S. Poyrazoglu, A. Topaloğlu, L. D. Kotan, 2012, Journal of Clinical Research in Pediatric Endocrinology.

A Duplication Upstream of SOX9 Associated with SRY Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report

E. Mengen, S. A. Uçaktürk, G. Kayhan, 2020, Journal of clinical research in pediatric endocrinology.

Emotion dysregulation and pediatric obesity: investigating the role of Internet addiction and eating behaviors on this relationship in an adolescent sample

E. Mengen, O. Uneri, S. A. Uçaktürk, 2020, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

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

E. Mengen, S. Neşelioğlu, Ö. Erel, 2020, Journal of clinical research in pediatric endocrinology.