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
Şahin

Cem Şahin

The Relationship Between Gestational Diabetes Mellitus and Selenoprotein-P Plasma 1 (SEPP1) Gene Polymorphisms

(J Clin Res Pediatr Endocrinol 2017; 9: 28-28)

Monogenic Diabetes Case Presented with Symptomatic Hyperglycemia and Atypical Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 14-14)

New Chromosomal ins(6;7)(Q13:P22) Anomaly in Klinefelter Syndrome Detected Coincidentally in Patient with Signs of Primary Hypogonadism

(J Clin Res Pediatr Endocrinol 2017; 9: 12-12)

Incidentally Detected Monogenic Diabetes Case

(J Clin Res Pediatr Endocrinol 2017; 9: 6-6)

Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 187-191)

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 74-79)
Şanlıdağ

Burçin Şanlıdağ

The Role of Adenovirus Serotype 36 in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2017; 9: 3-3)

The Role of Adenovirus Serotype 36 in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2017; 9: 3-3)
Şarer Yürekli

Banu Şarer Yürekli

Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 26-26)

Two Cases of Testicular Adrenal Rest Tumor (TART)

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

A Case Report of Seckel Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 13-13)

Osteogenesis Imperfecta: Case Report

(J Clin Res Pediatr Endocrinol 2017; 9: 11-11)

A Case of MEN 2A: D631Y Mutation

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

Two Cases of Klinefelter Syndrome

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

Aşkın Şen

Pseudohypoparathyroisidm Type 1a: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 15-15)

Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 13-13)

Persistent Müllerian Duct Syndrome with Transverse Testicular Ectopia: A Novel Anti-Müllerian Hormone Receptor Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 179-181)

Ghrelin Levels in Children with Constitutional Delay of Growth and Puberty - Original Article

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

The Relationship Between Serum Adiponectin, Tumor Necrosis Factor-Alpha, Leptin Levels and Insulin Sensitivity in Childhood and Adolescent Obesity: Adiponectin is a Marker of Metabolic Syndrome - Original Article

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

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

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

A Case of Hypocalciuric Hypercalcemia Accompanying Cystic Fibrosis

(J Clin Res Pediatr Endocrinol 2015; 7: 62-62)

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

(J Clin Res Pediatr Endocrinol 2015; 7: 183-191)

Heart-Type Fatty Acid Binding Protein Level as a Tool in Identification of Early Cardiac Effects of Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2017; 9: 118-123)

Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation

(J Clin Res Pediatr Endocrinol 2017; 9: 13-13)
Şentürk Mutlu

Fatma Şentürk Mutlu

Testicular Adrenal Rest Tumors in Patients with Congenital Adrenal Hyperplasia

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

Zeynep Şıklar

Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study - Original Article

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

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: -)

Combined Evaluation of IGF-1 and IGFBP-3 as an Index of Efficacy and Safety in Growth Hormone Treated Patients - Original Article

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

Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age - Original Article

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

Long-Term Follow-Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5 - Case Report

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

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

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

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA-Genotyping Results-Original Article

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

Two Siblings with Isolated GH Deficiency Due to Loss-of-Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation-Case Report

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

Evaluation of Thyroid Functions with Respect to Iodine Status and TRH Test in Chronic Autoimmune Thyroiditis - Original Article

(J Clin Res Pediatr Endocrinol 2011; 3: -)

Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties - Case Report

(J Clin Res Pediatr Endocrinol 2011; 3: -)

Efficiency of Fluid Treatments with Different Sodium Concentration in Children with Type 1 Diabetic Ketoacidosis

(J Clin Res Pediatr Endocrinol 2011; 3: -)

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: -)

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

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

Relationships Between Osteocalcin, Glucose Metabolism and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?

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

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

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

Syndromic Disorders with Short Stature

(J Clin Res Pediatr Endocrinol 2014; 6: 1-8)

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

(J Clin Res Pediatr Endocrinol 2014; 6: 254-257)

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 37-44)

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)

Tamoxifen Treatment for Pubertal Gynecomastia in a Patient with Partial Androgen Insensitivity Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 76-76)

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

(J Clin Res Pediatr Endocrinol 2015; 7: 301-306)

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

(J Clin Res Pediatr Endocrinol 2016; 8: 144-149)

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

(J Clin Res Pediatr Endocrinol 2016; 8: 211-217)

Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis

(J Clin Res Pediatr Endocrinol 2016; 8: 276-281)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

(J Clin Res Pediatr Endocrinol 2016; 8: 305-312)

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 375-380)

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

(J Clin Res Pediatr Endocrinol 2017; 9: 163-167)

Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

(J Clin Res Pediatr Endocrinol 2017; 9: 168-171)
Şimsek

Damla Gökşen Şimsek

Mutation Spectrum of GCK, HNF1A, and HNF1B in MODY Patients and 40 Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 22-22)
Şimşek

Damla Gökşen Şimşek

Anthropometric Measurements and Complications of Achondroplasia Patients

(J Clin Res Pediatr Endocrinol 2017; 9: 22-22)

A Novel Pathogenic DNA Variation in the OCRL1 Gene in Lowe Syndrome - Case Report

(J Clin Res Pediatr Endocrinol 2011; 3: -)

Increased Thrombin-Activatable Fibrinolysis Inhibitor and Decreased Tissue Factor Pathway Inhibitor and Thrombomodulin Levels in Children with Hypothyroidism

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

Premature Menarche Associated with McCune-Albright Syndrome in an Infant

(J Clin Res Pediatr Endocrinol 2015; 7: 11-11)

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

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

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 37-44)

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

(J Clin Res Pediatr Endocrinol 2015; 7: 183-191)

Cellular Trace Element Changes in Type 1 Diabetes Patients

(J Clin Res Pediatr Endocrinol 2016; 8: 180-186)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

(J Clin Res Pediatr Endocrinol 2016; 8: 305-312)

Gonadoblastoma and Papillary Tubal Hyperplasia in Ovotesticular Disorder of Sexual Development

(J Clin Res Pediatr Endocrinol 2016; 8: 351-355)

A Novel Pathogenic DNA Variation in the OCRL1 Gene in Lowe Syndrome - Case Report

(J Clin Res Pediatr Endocrinol 2011; 3: -)

Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 13-20)
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