AUTHOR INDEX

A B C Ç D E F G H I İ J K L M N O Ö P R S Ş T U Ü V Y Z
Fabricio

Gabriel Fabricio

Environmental Contaminants and Pancreatic Beta-Cells

(J Clin Res Pediatr Endocrinol 2016; 8: 257-263)
Faendrich

Fred Faendrich

Generation of Monocyte-Derived Insulin-Producing Cells from Non-Human Primates According to an Optimized Protocol for the Generation of PCMO-Derived Insulin-Producing Cells

(J Clin Res Pediatr Endocrinol 2014; 6: 93-99)
Fajkusova

Lenka Fajkusova

A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 482-483)
Faska

Barbara Kalina Faska

L-thyroxine Stabilizes Autoimmune Inflammatory Process in Euthyroid Nongoitrous Children with Hashimoto’s Thyroiditis and Type 1 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2013; 5: -)
Felius

Abraham Felius

Vitamin D Deficiency in Pediatric Fracture Patients: Prevalence, Risk Factors, and Vitamin D Supplementation

(J Clin Res Pediatr Endocrinol 2016; 8: 445-451)
Fendler

Wojciech Fendler

L-thyroxine Stabilizes Autoimmune Inflammatory Process in Euthyroid Nongoitrous Children with Hashimoto’s Thyroiditis and Type 1 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2013; 5: -)
Feng

Tian Feng

Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis

(J Clin Res Pediatr Endocrinol 2016; 8: 135-143)

Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

(J Clin Res Pediatr Endocrinol 2016; 8: 405-410)
Ferrero

Giovanni Battista Ferrero

Thyroid Involvement in Two Patients with Bannayan-Riley-Ruvalcaba Syndrome

(J Clin Res Pediatr Endocrinol 2013; 5: -)
Feyles

Francesca Feyles

Thyroid Involvement in Two Patients with Bannayan-Riley-Ruvalcaba Syndrome

(J Clin Res Pediatr Endocrinol 2013; 5: -)
Fidancı

Kürşad Fidancı

Ghrelin Levels and Postnatal Growth in Healthy Infants 0-3 Months of Age - Original Article

(J Clin Res Pediatr Endocrinol 2010; 2: -)

Metabolic and Histopathological Effects of Fructose Intake During Pregestation, Gestation and Lactation in Rats and their Offspring

(J Clin Res Pediatr Endocrinol 2015; 7: 19-26)

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

(J Clin Res Pediatr Endocrinol 2015; 7: 27-36)
Fingert

Sarabeth Broder Fingert

Evaluation of Adolescents for Polycystic Ovary Syndrome in an Urban Population - Original Article

(J Clin Res Pediatr Endocrinol 2009; 1: 188-193)
Fitoz

Suat Fitoz

Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow-up - Case Report

(J Clin Res Pediatr Endocrinol 2008; 1: -)
Fitöz

Ömer Suat Fitöz

A Case of Pycnodysostosis with Bilateral Choanal Atresia

(J Clin Res Pediatr Endocrinol 2015; 7: 70-70)

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

(J Clin Res Pediatr Endocrinol 2010; 2: -)

Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism

(J Clin Res Pediatr Endocrinol 2012; 4: -)
Flanagan

Sarah E. Flanagan

A Combination of Nifedipine and Octreotide Treatment in an Hyperinsulinemic Hypoglycemic Infant

(J Clin Res Pediatr Endocrinol 2014; 6: 119-121)

A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

(J Clin Res Pediatr Endocrinol 2015; 7: 144-147)

Nifedipine in Congenital Hyperinsulinism-A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 151-154)

Efficacy and Safety of Sirolimus (mTOR Inhibitor) in Two Patients with Diazoxide-Unresponsive Hyperinsulinemic Hypoglycemia

(J Clin Res Pediatr Endocrinol 2015; 7: 86-86)

Successful Transfer from Insulin to Oral Sulphonylurea in an Infant and His Mother with Monogenic Diabetes Due to a Heterozygous Missense Mutation in the ABCC8 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 86-86)

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism

(J Clin Res Pediatr Endocrinol 2016; 8: 197-204)

A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus

(J Clin Res Pediatr Endocrinol 2016; 8: 478-481)
Flanagan Sarah

E. Flanagan Sarah

Transient Neonatal Diabetes Mellitus in a Turkish Patient with Three Novel Homozygous Variants in the ZFP57 Gene

(J Clin Res Pediatr Endocrinol 2013; 5: -)
Fonte

Maria Luisa Fonte

Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports

(J Clin Res Pediatr Endocrinol 2016; 8: 250-256)
Fonvig

Cilius Esmann Fonvig

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

(J Clin Res Pediatr Endocrinol 2017; 9: 8-16)
Friger

Michael Friger

Pubertal Gynecomastia Coincides with Peak Height Velocity

(J Clin Res Pediatr Endocrinol 2013; 5: -)
Fukami

Maki Fukami

A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 344-348)
Furman

Andrzej Furman

Z-Score Reference Values for Height in Turkish Children Aged 6 to 18 Years

(J Clin Res Pediatr Endocrinol 2014; 6: -)

Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children

(J Clin Res Pediatr Endocrinol 2015; 7: 280-293)
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