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
Sağ

Erdal Sağ

Hyperthyroidism After Allogeneic Hematopoietic Stem Cell Transplantation: A Report of Four Cases

(J Clin Res Pediatr Endocrinol 2015; 7: 349-354)
Sağlam

Celal Sağlam

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)

Prevalence and Correlates of Obesity in Schoolchildren from the City of Bursa,Turkey - Original Article

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

A Rare Cause of Precocious Puberty: Hepatoblastoma - Case Report

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

Acquired Generalized Lipodystrophy Associated with Autoimmune Hepatitis and Low Serum C4 Level - Case Report

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

Clinical Course of Hyperprolactinemia in Children and Adolescents: A Review of 21 Cases - Original Article

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

Thyroid Functions in Long-Term Survivors of Pediatric Hodgkin’s Lymphoma Treated with Chemotherapy and Radiotherapy - Original Article

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

Resolution of Autoimmune Oophoritis after Thymectomy in a Myasthenia Gravis Patient

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

Testicular Adrenal Rest Tumors in Patients with Congenital Adrenal Hyperplasia

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

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

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

An Obese Case with Homozygous Leptin Receptor Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 60-60)

A Case of Odontohypophosphatasia and Family Investigation

(J Clin Res Pediatr Endocrinol 2015; 7: 67-67)

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)

Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases

(J Clin Res Pediatr Endocrinol 2016; 8: 330-333)

One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism

(J Clin Res Pediatr Endocrinol 2014; 6: 169-173)
Sahip

Yusuf Sahip

Food Types in the Diet and the Nutrient Intake of Obese and Non-Obese Children - Original Article

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

Emi Saito

Heparin-Induced Hyperkalemia in an Extremely-Low-Birth-Weight Infant: A Case Report

(J Clin Res Pediatr Endocrinol 2014; 6: 125-128)
Saka

Hatice Nurçin Saka

Anthropometric Studies on the Turkish 
Population - A Historical Review

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

Puberty and Pubertal Growth in Healthy Turkish Girls: No evidence for secular trend - Original Article

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

CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype-phenotype correlation in Turkish children - Original Article

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

A Patient with 22q11.2 Deletion Syndrome: case report - Case Report

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

Permanent Neonatal Diabetes Mellitus: Same Mutation, Different Glycemic Control with Sulfonylurea Therapy on Long-Term Follow-up

(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: -)

Is Premature Thelarche in the First Two Years of Life Transient?

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

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

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

Epidemiologic Features of Type 1 Diabetic Patients between 0 and 18 Years of Age in İstanbul City

(J Clin Res Pediatr Endocrinol 2015; 7: 49-56)

Central Precocious Puberty in a Patient with Multiple Pituitary Hormone Deficiency Due to POU1F1 (PIT1) Gene Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 72-72)
Sakr

Maha Mahmoud Hamed Sakr

The Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in Children

(J Clin Res Pediatr Endocrinol 2016; 8: 399-404)
Salas-Fernández

Alejandra Salas-Fernández

The 13C-Glucose Breath Test for Insulin Resistance Assessment in Adolescents: Comparison with Fasting and Post-Glucose Stimulus Surrogate Markers of Insulin Resistance

(J Clin Res Pediatr Endocrinol 2016; 8: 419-424)
Saldır

Mehmet Saldır

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)

Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 340-343)
Saleh

Rabab M. Saleh

The Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in Children

(J Clin Res Pediatr Endocrinol 2016; 8: 399-404)

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

(J Clin Res Pediatr Endocrinol 2016; 8: 461-467)
Salehian

Behrouz Salehian

RET Gene Abnormalities and Thyroid Disease: Who Should be Screened and When

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

Functioning Adrenocortical Tumors in 
Children-Secretory Behavior

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

Grosso Salvatore

Thyroid Function in Small for Gestational Age Newborns: A Review

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

Raynald Samoa

RET Gene Abnormalities and Thyroid Disease: Who Should be Screened and When

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

Tanzer Sancak

Neurocognitive Functions in Children and Adolescents with Subclinical Hypothyroidism

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

Rukiye Sancı

Hidden Toxicity in Neonatal Intensive Care Units: Phthalate Exposure in Very Low Birth Weight Infants

(J Clin Res Pediatr Endocrinol 2016; 8: 298-304)
Sandal

Gonca Sandal

Social Anxiety, Depression and Self-Esteem in Obese Adolescent Girls with Acanthosis Nigricans

(J Clin Res Pediatr Endocrinol 2015; 7: 63-68)
Sander

Serdar Sander

Fetal-Neonatal Ovarian Cysts-Their Monitoring and Management: Retrospective Evaluation of 20 Cases and Review of the Literature - Original Article

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

Daksha Sanghavi

Identification of Novel Mutations in STAR Gene in Patients with Lipoid Congenital Adrenal Hyperplasia: A First Report from India

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

Özlem Sangun

Prevalence of Metabolic Syndrome in Obese Children and Adolescents using Three Different Criteria and Evaluation of Risk Factors - Original Article

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

Özlem Sangün

ABCC8 Frameshift Mutation in Exon 28 (c.3512delT) is a Founder Mutation for Autosomal Recessive Hyperinsulinemic Hypoglycemia in Eastern Anatolia

(J Clin Res Pediatr Endocrinol 2015; 7: 20-20)

The Effects of Six-Month L-Thyroxine Treatment on Cognitive Functions and Event-Related Brain Potentials in Children with Subclinical Hypothyroidism

(J Clin Res Pediatr Endocrinol 2015; 7: 102-108)

Mozaic Turner Syndrome and Precocious Puberty Association: A Three-Year-Old Patient

(J Clin Res Pediatr Endocrinol 2015; 7: 58-58)
Santanera

Arianna Santanera

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

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

Nappini Sara

Thyroid Function in Small for Gestational Age Newborns: A Review

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

Adrijan Sarajlija

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

(J Clin Res Pediatr Endocrinol 2016; 8: 228-231)
Sarı

Erkan Sarı

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)

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)

Investigation of Genes That are Defined with New Generation Sequence Analysis in Children/Adolescents Followed with Maturity Onset Diabetes of the Young

(J Clin Res Pediatr Endocrinol 2015; 7: 46-46)

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)

Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 340-343)

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)

Inflammatory Myofibroblastic Tumor Presenting with Diabetes Insipidus in an Eight-Year-Old Boy: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 340-343)
Sarıcı

Dilek Sarıcı

Fetal Adrenal Suppression Due to Maternal Corticosteroid Use: Case Report

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

Follow-Up During Early Infancy of Newborns Diagnosed with Subcutaneous Fat Necrosis

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

Serdar Sarıtaş

A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty

(J Clin Res Pediatr Endocrinol 2016; 8: 232-235)
Satan

Ali Satan

A Patient with 22q11.2 Deletion Syndrome: case report - Case Report

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

İlhan Satman

Wolfram Syndrome: Presentation of Two Cases with Type One and Type Two Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2015; 7: 69-69)
Saucedo

Renata Saucedo

Lower Plasma Ghrelin Levels are Found in Women with Diabetes-Complicated Pregnancies

(J Clin Res Pediatr Endocrinol 2016; 8: 425-431)
Savage

David B. Savage

Familial Partial Lipodystrophy Linked to aNovel Peroxisome Proliferator-Activated Receptor -γ (PPARG) Mutation, H449L

(J Clin Res Pediatr Endocrinol 2015; 7: 92-92)
Savaş

Tülün Savaş

Mozaic Turner Syndrome and Precocious Puberty Association: A Three-Year-Old Patient

(J Clin Res Pediatr Endocrinol 2015; 7: 58-58)
Savaş Erdeve

Şenay Savaş Erdeve

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: -)

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: -)

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: -)

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: -)

Hyperinsulinemic Hypoglycemia: Experience in A Series of 17 Cases

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

Familial Partial Lipodystrophy Linked to aNovel Peroxisome Proliferator-Activated Receptor -γ (PPARG) Mutation, H449L

(J Clin Res Pediatr Endocrinol 2015; 7: 92-92)

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)

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)

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

(J Clin Res Pediatr Endocrinol 2017; 9: 91-94)
Savaş-Erdeve

Şenay Savaş-Erdeve

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)
Say

Aysu Say

Critical Points in the Management of Pseudohypoaldosteronism Type 1 - Case Report

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

L. Füsun Saygılı

A Case of Polyglandular Autoimmune Syndrome Type One with Hypercalcemia and Hypotension

(J Clin Res Pediatr Endocrinol 2015; 7: 51-51)

Aromatase Deficiency, a Rare Syndrome: Case Report

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

A Young Diabetic Case with Bloom Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 42-42)

A Case of Dyskeratosis Congenita Associated with Hypothyroidism and Hypogonadism

(J Clin Res Pediatr Endocrinol 2015; 7: 42-42)

Melanocortin-4 Receptor Mutation and Obesity

(J Clin Res Pediatr Endocrinol 2015; 7: 43-43)

Multiple Endocrine Neoplasia Type 4 (MEN4) Syndrome

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

Olfactory Sulcus Hypoplasia Images in a Case of Kallmann Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 49-49)

A Novel Mutation in Deficiency of 11 β-Hydroxylase: A Possible Association with Disease Severity

(J Clin Res Pediatr Endocrinol 2015; 7: 50-50)

Features of Nine Adult Cases of Osteogenesis Imperfecta

(J Clin Res Pediatr Endocrinol 2015; 7: 52-52)

Heterozygous AGPAT2 Mutation, Diabetes, and Lipodystrophy in Extremities

(J Clin Res Pediatr Endocrinol 2015; 7: 53-53)

Magnetic Resonance Imaging Characteristics of a Dunnigan-Type Familial Partial Lipodystrophy Patient

(J Clin Res Pediatr Endocrinol 2015; 7: 61-61)
Schaefer

Franz Schaefer

Averting the Legacy of Kidney Disease-Focus on Childhood

(J Clin Res Pediatr Endocrinol 2016; 8: 108-113)
Schepper

Jean De Schepper

Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 86-91)
Schipper

Inger B. Schipper

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

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

Karl Peter Schlingmann

A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 101-104)
Schulze

Maren Schulze

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)
Seçil

Mustafa Seçil

Magnetic Resonance Imaging Characteristics of a Dunnigan-Type Familial Partial Lipodystrophy Patient

(J Clin Res Pediatr Endocrinol 2015; 7: 61-61)
Seiler

Kelly J. Seiler

Morning Cortisol Levels Affected by Sex and Pubertal Status in Children and Young Adults

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

Beray Selver Eklioğlu

Absence of Increase in Carotid Artery Intima-Media Thickness in Infants of Diabetic Mothers

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

The Relationship Between Metabolic Syndrome and Left Ventricular Mass Index in Obese Children-

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

Association Between Apolipoprotein E Polymorphism and Subclinic Atherosclerosis in Patients with Type 1 Diabetes Mellitus

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

Reevaluation of the Prevalence of Metabolic 
Syndrome in an Urban Area of Turkey

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

Ambulatory Blood Pressure and Subclinical Cardiovascular Disease in Patients with Congenital Adrenal Hyperplasia: A Preliminary Report

(J Clin Res Pediatr Endocrinol 2015; 7: 13-18)

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

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

Senthil Senniappan

Fluoxetine-Induced Hypoglycaemia in a Patient with Congenital Hyperinsulinism on Lanreotide Therapy

(J Clin Res Pediatr Endocrinol 2016; 8: 347-350)
Serdar

Muhiddin Serdar

The Effect of Insulin Resistance and Obesity on Low-Density Lipoprotein Particle Size in Children - Original Article

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

Hepsen Mine Serin

Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 192-196)
Sert

Ahmet Sert

Relationship Between Aspartate Aminotransferase-to-Platelet Ratio Index and Carotid Intima-Media Thickness in Obese Adolescents with Non-Alcoholic Fatty Liver Disease

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

Betül Sevinir

A Rare Cause of Precocious Puberty: Hepatoblastoma - Case Report

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

Thyroid Functions in Long-Term Survivors of Pediatric Hodgkin’s Lymphoma Treated with Chemotherapy and Radiotherapy - Original Article

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

Gülcan Seymen Karabulut

Attitudes of Pediatricians Regarding Prevention and Treatment of Vitamin D Deficiency

(J Clin Res Pediatr Endocrinol 2016; 8: 368-371)
Sezer

Atakan Sezer

Investigation of BRAF Hotspot Mutations in Papillary Thyroid Tumor Samples

(J Clin Res Pediatr Endocrinol 2015; 7: 68-68)

Effect of Maternal Factors and Fetomaternal Glucose Homeostasis on Birth Weight and Postnatal Growth

(J Clin Res Pediatr Endocrinol 2015; 7: 168-174)
Shah

Bina Shah

The Relationship Between Leptin and Norepinephrine Levels During OGTT in Normotensive and Hypertensive Obese Adolescents - Original Article

(J Clin Res Pediatr Endocrinol 2009; 1: 175-180)

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

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

A Novel Mutation Causing Pseudohypoparathyroidism 1A with Congenital Hypothyroidism and Osteoma Cutis - Case Report

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

The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia

(J Clin Res Pediatr Endocrinol 2015; 7: 86-97)
Shaikh

Adnan Al Shaikh

Impact of Vitamin D Status on Cardiometabolic Complications among Children and Adolescents with Type 1 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2016; 8: 48-54)

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

(J Clin Res Pediatr Endocrinol 2016; 8: 461-467)
Shalet

Stephen M. Shalet

Management of Growth Hormone Deficiency in Children Irradiated for Brain Tumours

(J Clin Res Pediatr Endocrinol 2015; 7: 4-4)
Shaneen

Ranad Shaneen

A Case of Achondrogenesis Type 2/Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 80-80)
Shao

Xiao-Juan Shao

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

(J Clin Res Pediatr Endocrinol 2016; 8: 224-227)
Sharma

Akshat Sharma

Safety and Efficacy of Stosstherapy in Nutritional Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 63-69)

Safety and Efficacy of Stosstherapy in Nutritional Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 63-69)
Shchelochkov

Oleg A. Shchelochkov

Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia

(J Clin Res Pediatr Endocrinol 2017; 9: 70-73)
Sheng

Huiying Sheng

Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy

(J Clin Res Pediatr Endocrinol 2017; 9: 52-57)
Sherief

Laila Metwaly Sherief

The Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in Children

(J Clin Res Pediatr Endocrinol 2016; 8: 399-404)
Shimokaze

Tomoyuki Shimokaze

Heparin-Induced Hyperkalemia in an Extremely-Low-Birth-Weight Infant: A Case Report

(J Clin Res Pediatr Endocrinol 2014; 6: 125-128)
Shin

Jae-Gook Shin

A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans

(J Clin Res Pediatr Endocrinol 2016; 8: 205-210)
Shuaibi

Ahmed Al Shuaibi

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

(J Clin Res Pediatr Endocrinol 2016; 8: 461-467)
Sıdal

Müjgan Sıdal

Clinical and Laboratory Characteristics of Children Referred for Early Puberty: Preponderance in 7-8 Years of Age

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

Tania Siahanidou

Identification and Functional Characterization of a Calcium-Sensing Receptor Mutation in an Infant with Familial Hypocalciuric Hypercalcemia

(J Clin Res Pediatr Endocrinol 2016; 8: 341-346)
Silce

Caroline Silce

A Rare GCMB Gene Mutation in an Isolated Hypoparathyroidism Case

(J Clin Res Pediatr Endocrinol 2015; 7: 59-59)
Simpser

Tamar Simpser

Update on Some Aspects of Neonatal Thyroid Disease - Review

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

Yashpal Singh

A Study of Insulin Resistance by HOMA-IR and its Cut-off Value to Identify Metabolic Syndrome in Urban Indian Adolescents

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

Betül Siyah Bilgin

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)
Skotakova

Jarmila Skotakova

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)
Smuts

Cornelius M. Smuts

Breast-Milk Iodine Concentrations, Iodine Status, and Thyroid Function of Breastfed Infants Aged 2-4 Months and Their Mothers Residing in a South African Township

(J Clin Res Pediatr Endocrinol 2016; 8: 381-391)
Soliman

Ashraf Soliman

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

(J Clin Res Pediatr Endocrinol 2016; 8: 461-467)
Solmaz

Abdullah Solmaz

Serum Paraoxonase/Arylesterase Activity and Oxidative Stress Status in Children with Metabolic Syndrome

(J Clin Res Pediatr Endocrinol 2014; 6: 163-168)

Phenotype-Genotype Correlations in Bardet-Biedl Syndrome Patients with Molecular Analysis

(J Clin Res Pediatr Endocrinol 2015; 7: 82-82)
Solomon

Daniel Solomon

Pediatric Thyroid Disease: When is Surgery Necessary, and Who Should be Operating on Our Children?

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

Akbar Soltani

SLC34A3 Intronic Deletion in a New Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria

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

Julie Ann Sosa

Pediatric Thyroid Disease: When is Surgery Necessary, and Who Should be Operating on Our Children?

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

Narumi Sotoshi

Genetic Analysis in Our Cases with Thyroid Dysgenesis

(J Clin Res Pediatr Endocrinol 2015; 7: 77-77)
Soyaltın

Eren Soyaltın

A Case with Acrodysostosis and Hormone Resistance

(J Clin Res Pediatr Endocrinol 2015; 7: 75-75)
Soygür

Tarkan Soygür

Transverse Testicular Ectopia: A Rare Presentation with Persistent Müllerian Duct Syndrome

(J Clin Res Pediatr Endocrinol 2014; 6: 180-182)
Soylu

Nusret Soylu

Importance of Insulin Immunoassays in the Diagnosis of Factitious Hypoglycemia

(J Clin Res Pediatr Endocrinol 2014; 6: 258-261)
Soyluk Selçukbiricik

Özlem Soyluk Selçukbiricik

Osteogenesis Imperfecta Presenting with Fractures in Pregnancy or Lactation Period: Report of Three Cases

(J Clin Res Pediatr Endocrinol 2015; 7: 82-82)
Soyucen

Erdoğan Soyucen

Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene

(J Clin Res Pediatr Endocrinol 2016; 8: 360-364)
Soyuçen

Erdoğan Soyuçen

An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 79-79)
Söbü

Elif Söbü

An Obese Case with Homozygous Leptin Receptor Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 60-60)

Genotype-Phenotype Correlation of Congenital Adrenal Hyperplasia Cases Having Complex (Multiple) Mutation Detected in CYP21A2 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 88-88)
Söylemez

Feride Söylemez

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

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

Figen Söylemezoğlu

Primary Melanocytic Suprasellar Tumor Presenting with Growth Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2015; 7: 15-15)
Sözbilen

Murat Sözbilen

Multiple Endocrine Neoplasia Type 4 (MEN4) Syndrome

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

Chutintorn Sriphrapradang

A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient

(J Clin Res Pediatr Endocrinol 2016; 8: 241-245)
Stalman

Susanne E. Stalman

Diagnostic Work-up and Follow-up in Children with Tall Stature: A Simplified Algorithm for Clinical Practice

(J Clin Res Pediatr Endocrinol 2015; 7: 260-267)
Staník

Juraj Staník

Lack of Association Between Peripheral Activity of Thyroid Hormones and Elevated TSH Levels in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2014; 6: 100-104)
Staníková

Daniela Staníková

Lack of Association Between Peripheral Activity of Thyroid Hormones and Elevated TSH Levels in Childhood Obesity

(J Clin Res Pediatr Endocrinol 2014; 6: 100-104)
Straseski

Joely A. Straseski

Pediatric Reference Intervals for Free Thyroxine and Free Triiodothyronine by Equilibrium Dialysis-Liquid Chromatography-Tandem Mass Spectrometry

(J Clin Res Pediatr Endocrinol 2016; 8: 26-31)
Stratakis

Constantine A. Stratakis

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

(J Clin Res Pediatr Endocrinol 2016; 8: 468-471)
Street

Maria Elisabeth Street

Thyroid Disease in Childhood: An Update

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

Xueying Su

Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy

(J Clin Res Pediatr Endocrinol 2017; 9: 52-57)
Sultan Tosun

Mahya Sultan Tosun

A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report

(J Clin Res Pediatr Endocrinol 2016; 8: 101-104)
Sumathipala

Dulika Sumathipala

An Infant Born to a Mother with Gestational Diabetes Presenting with 49,XXXXY Syndrome and Renal Agenesis-A Case Report

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

Jia-Zhong Sun

Low-Grade Inflammation and Increased Arterial Stiffness in Chinese Youth and Adolescents with Newly-Diagnosed Type 2 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2015; 7: 268-273)

Low-Grade Inflammation and Increased Arterial Stiffness in Chinese Youth and Adolescents with Newly-Diagnosed Type 2 Diabetes Mellitus

(J Clin Res Pediatr Endocrinol 2015; 7: 268-273)

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

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

Hana Al Suwaidi

Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene

(J Clin Res Pediatr Endocrinol 2016; 8: 236-240)
Süleymanoğlu

Selami Süleymanoğlu

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

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

Two Siblings with Mutation in the Leptin Receptor Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 68-68)

Urinary Netrin-1: A New Biomarker for the Early Diagnosis of Renal Damage in Obese Children

(J Clin Res Pediatr Endocrinol 2016; 8: 282-287)

The Association between Serum 25-Hydroxy Vitamin D Level and Urine Cathelicidin in Children with a Urinary Tract Infection

(J Clin Res Pediatr Endocrinol 2016; 8: 325-329)
Swamy

Mathad K. S. Swamy

Safety and Efficacy of Stosstherapy in Nutritional Rickets

(J Clin Res Pediatr Endocrinol 2017; 9: 63-69)
Szadkowska

Agnieszka Szadkowska

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: -)
Szypowska

Agnieszka Szypowska

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: -)
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