M. Demiral

发表

Metastatic Papillary Thyroid Carcinoma in an Autonomous Hyperfunctioning Thyroid Nodule in an Adolescent: Case Report and Literature Review

H. Ilhan, E. Şimşek, E. Ihtiyar, 2014 .

Growth hormone and the risk of atherosclerosis in growth hormone-deficient children.

P. Koşger, E. Şimşek, Z. Kılıç, 2015, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

A novel diagnostic tool for the evaluation of hypothalamic-pituitary region and diagnosis of growth hormone deficiency: pons ratio

H. Demirbilek, E. Unal, M. Demiral, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

The Frequency of Metabolic Syndrome and Serum Osteopontin Levels in Survivors of Childhood Acute Lymphoblastic Leukemia.

B. Kırel, Z. Özdemir, Özcan Bör, 2018, Journal of adolescent and young adult oncology.

Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious Puberty

B. Kırel, E. Şimşek, S. Ceylaner, 2016, Hormone Research in Paediatrics.

Vitamin D Levels in Children Admitted to the Endocrine Outpatient Clinic

B. Kırel, M. Demiral, B. Sırmagül, 2016 .

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

A. Öztürk, S. Poyrazoglu, F. Baş, 2020, Journal of clinical research in pediatric endocrinology.

Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of life

K. Hussain, M. Ozbek, H. Demirbilek, 2020, Pediatric diabetes.

The Assessment of the Quality of Life in Children with Chronic Liver Disease.

D. Altay, T. Özgür, M. Demiral, 2021, The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology.

A Retrospective Analysis of Children and Adolescents With Diabetic Ketoacidosis in the Intensive Care Unıt: Is It Significant that the Blood Ketone Level Becomes Negative in Diabetic Ketoacidosis?

M. Ozbek, S. Tanrıverdi Yılmaz, E. Unal, 2020, Cureus.

Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations

A. Hattersley, A. Çayır, S. Flanagan, 2020, The Journal of clinical endocrinology and metabolism.

Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development

M. Üstün, E. Şimşek, B. Tokar, 2016, Journal of clinical research in pediatric endocrinology.

Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency

A. Latronico, L. Montenegro, E. Şimşek, 2015, Hormone Research in Paediatrics.

Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review

M. N. Özbek, S. Ceylaner, E. Unal, 2020, Hormones.

A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency

M. N. Özbek, H. Demirbilek, E. Unal, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 Gene

C. Durmaz, H. Demirbilek, S. Ceylaner, 2019, Journal of clinical research in pediatric endocrinology.

Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism

H. Demirbilek, E. Unal, M. Demiral, 2020, Journal of clinical research in pediatric endocrinology.

A novel mutation in a case of pseudohypoparathyroidism type Ia.

B. Kırel, K. Karaer, M. Demiral, 2016, The Turkish journal of pediatrics.

Severe consumptive hypothyroidism caused by multiple infantile hepatic haemangiomas

E. Şimşek, M. Demiral, Elif Gundogdu, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

Horner Syndrome Secondary to Thyroid Surgery

H. Ilhan, E. Şimşek, Ç. Binay, 2017, Case reports in endocrinology.

Neonatal Hypercalcaemia Associated with Congenital Adrenal Hyperplasia

N. Tekin, E. Şimşek, Ç. Binay, 2014 .

EVALUATION OF THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS IN A PAEDIATRIC INTENSIVE CARE UNIT.

E. Şimşek, E. Dinleyici, M. Demiral, 2019, Acta endocrinologica.

Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-Eastern Region of Turkey

H. Demirbilek, E. Unal, M. Demiral, 2020, Journal of clinical research in pediatric endocrinology.

Early puberty paradox: an investigation of anxiety levels of mothers and children, children's quality of life, and psychiatric diagnoses.

M. Demiral, Ö. Kardaş, Burcu Kardaş, 2023, European journal of pediatrics.

Evaluation of clinical and laboratory findings in the differential diagnosis of central precocious puberty and premature thelarche

E. Unal, M. Demiral, A. Beştaş, 2023, Indian journal of endocrinology and metabolism.

Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes

M. Ağın, H. Demirbilek, E. Unal, 2020, Journal of clinical research in pediatric endocrinology.

A novel diagnostic tool in determining insulin resistance in obese children: Triglyceride / HDL ratio

M. Demiral, 2021, Journal of Surgery and Medicine.

Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

A. Çayır, B. Cavdarli, K. Hussain, 2020, Journal of clinical research in pediatric endocrinology.

Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year

H. Onay, H. Demirbilek, Şervan Özalkak, 2022, Journal of clinical research in pediatric endocrinology.