Journal of Clinical Research in Pediatric Endocrinology

Papers
(The TQCC of Journal of Clinical Research in Pediatric Endocrinology is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-03-01 to 2024-03-01.)
ArticleCitations
New Features for Child Metrics: Further Growth References and Blood Pressure Calculations52
Metabolic Bone Disease in Premature Neonates: An Unmet Challenge29
Traditional and New Methods of Bone Age Assessment-An Overview26
Syndromic Disorders Caused by Disturbed Human Imprinting24
Triglyceride Glucose Index as a Surrogate Measure of Insulin Sensitivity in a Caucasian Pediatric Population21
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism19
Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes19
Endocrine Disruptors and Polycystic Ovary Syndrome: Phthalates18
Vitamin D Status Across Age Groups in Turkey: Results of 108,742 Samples from a Single Laboratory16
Current Diagnosis, Treatment and Clinical Challenges in the Management of Lipodystrophy Syndromes in Children and Young People15
Has the Frequency of Precocious Puberty and Rapidly Progressive Early Puberty Increased in Girls During the COVID-19 Pandemic?15
A Proposal for the Interpretation of Serum IGF-I Concentration as Part of Laboratory Screening in Children with Growth Failure15
How Vitamin D Levels of Children Changed During COVID-19 Pandemic: A Comparison of Pre-pandemic and Pandemic Periods15
Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism12
Prevalence of Obesity and Metabolic Syndrome in Children with Type 1 Diabetes: A Comparative Assessment Based on Criteria Established by the International Diabetes Federation, World Health Organisatio12
Detection of <i>SHOX</i> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature11
A Novel Missense Mutation in Human Receptor Roundabout-1 <i>(ROBO1)</i> Gene Associated with Pituitary Stalk Interruption Syndrome11
The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region10
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants10
Association of Exosomal miR-34a with Markers of Dyslipidemia and Endothelial Dysfunction in Children and Adolescents with T1DM9
Assessment of Bisphenol A Levels in Preschool Children: Results of a Human Biomonitoring Study in Ankara, Turkey8
A Long-Term Comparison of Presenting Characteristics of Children with Newly Diagnosed Type 1 Diabetes Before and During the COVID-19 Pandemic8
Association of Total and High Molecular Weight Adiponectin with Components of Metabolic Syndrome in Mexican Children8
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets8
Diagnostic Performance of Neck Circumference and Cut-off Values for Identifying Overweight and Obese Pakistani Children: A Receiver Operating Characteristic Analysis8
Increased Incidence of Type 1 Diabetes in Children and No Change in the Age of Diagnosis and BMI-SDS at the Onset - is the Accelerator Hypothesis not Working?8
Children with Hashimoto’s Thyroiditis Have Increased Intestinal Permeability: Results of a Pilot Study7
Urinary NGAL is a Potential Biomarker for Early Renal Injury in Insulin Resistant Obese Non-diabetic Children7
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome7
The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults7
Effects of 5-Hydroxymethylfurfural on Pubertal Development of Female Wistar Rats7
A Case of Familial Male-limited Precocious Puberty with a Novel Mutation6
Efficacy and Safety of Letrozole in the Management of Constitutional Delay in Growth and Puberty: A Systematic Review and Meta-analysis6
Current Treatments for Patients with Genetic Obesity6
Growth and Adult Height during Human Growth Hormone Treatment in Chinese Children with Multiple Pituitary Hormone Deficiency Caused by Pituitary Stalk Interruption Syndrome: A Single Centre Study6
Low Complement C1q/TNF-related Protein-13 Levels are Associated with Childhood Obesity But not Binge Eating Disorder6
The Significance of Thiol/Disulfide Homeostasis and Ischemia-modified Albumin Levels in Assessing Oxidative Stress in Obese Children and Adolescents6
Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia6
A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the <i>SAMD9</i> Gene6
An Evaluation of Glucagon Injection Anxiety and Its Association with the Fear of Hypoglycemia among the Parents of Children with Type 1 Diabetes6
Indonesian National Growth Reference Charts Better Reflect Height and Weight of Children in West Java, Indonesia, than WHO Child Growth Standards6
The Value of Telemedicine for the Follow-up of Patients with New Onset Type 1 Diabetes Mellitus During COVID-19 Pandemic in Turkey: A Report of Eight Cases5
Fibroblast Growth Factor 21 Levels and Bone Mineral Density in Metabolically Healthy and Metabolically Unhealthy Obese Children5
Can Nesfatin-1 Predict Hypertension in Obese Children?5
Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience5
TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys5
Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 25
Care and Support of Children with Type 1 Diabetes at School: The Turkish Experience5
Important Tools for Use by Pediatric Endocrinologists in the Assessment of Short Stature5
Bisphenol A Exposure in Exclusively Breastfed Infants and Lactating Women: An Observational Cross-sectional Study5
Different Potent Glucocorticoids, Different Routes of Exposure but the Same Result: Iatrogenic Cushing’s Syndrome and Adrenal Insufficiency5
Managing Paediatric Growth Disorders: Integrating Technology Into a Personalised Approach5
Soluble Receptor for Glycation End-products Concentration Increases Following the Treatment of Severe Diabetic Ketoacidosis5
Elevated Pre-injection Basal Luteinizing Hormone Concentrations are Common in Girls Treated for Central Precocious Puberty5
Heterozygous Insulin Receptor (INSR) Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series5
Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation5
Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the <i>CYP19A1</i> Gene5
Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience5
Very High Incidence of Type 1 Diabetes Among Children Aged Under 15 Years in Tlemcen, Northwest Algeria (2015-2018)5
Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism5
Precocious Puberty in Boys: A Study Based on Five Years of Data from a Single Center in Northern China4
Two Subsequent Metachroneus Solid Tumors: Oncocytic Variant Adrenocortical Carcinoma and Rhabdomyosarcoma of Childhood: Case Report and Literature Review4
Factors Affecting Thyroid Elastography in Healthy Children and Patients with Hashimoto’s Thyroiditis4
Girls with Premature Thelarche Younger than 3 Years of Age May Have Stimulated Luteinizing Hormone Greater than 10 IU/L4
A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia4
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in <i>CYP11B2</i>4
Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children4
Are Thyroid Functions Affected in Multisystem Inflammatory Syndrome in Children?4
A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome4
Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey4
Mutations Within the Transcription Factor <i>PROP1</i> in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency4
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 <i>GLI2</i&g4
A Duplication Upstream of SOX9 Associated with <i>SRY</i> Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report4
Midkine: Utility as a Predictor of Early Diabetic Nephropathy in Children with Type 1 Diabetes Mellitus4
IGFA Case Report of Pycnodysostosis Associated with Multiple Pituitary Hormone Deficiencies and Response to Treatment4
The Effectiveness of Sirolimus Treatment in Two Rare Disorders with Nonketotic Hypoinsulinemic Hypoglycemia: The Role of mTOR Pathway4
Clinical Management in Systemic Type Pseudohypoaldosteronism Due to <i>SCNN1B</i> Variant and Literature Review4
The Successful Treatment of Deep Soft-tissue Calcifications with Topical Sodium Thiosulphate and Acetazolamide in a Boy with Hyperphosphatemic Familial Tumoral Calcinosis due to a Novel Mutation in FG4
Vitamin D Deficiency Prevalence in Late Neonatal Hypocalcemia: A Multicenter Study4
Diagnostic Value of Bilateral Petrosal Sinus Sampling in Children with Cushing Disease: A Multi-center Study4
Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose?4
Cord Blood Levels of Spexin, Leptin, and Visfatin in Term Infants Born Small, Appropriate, and Large for Gestational Age and Their Association with Newborn Anthropometric Measurements3
Growth Hormone Treatment and Papilledema: A Prospective Pilot Study3
Primary Hyperparathyroidism Presenting as Posterior Reversible Encephalopathy Syndrome: A Report of Two Cases3
Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of GLIS3 Mutation3
Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success3
Time to the Peak, Shape of the Curve and Combination of These Glucose Response Characteristics During Oral Glucose Tolerance Test as Indicators of Early Beta-cell Dysfunction in Obese Adolescents3
Macular Variability in Children and Adolescents with Metabolic Syndrome: A Cross-sectional Study Examining the Associations with Anthropometric Measurements, Metabolic Parameters and Inflammatory Mark3
Syndrome of Congenital Insulin Resistance Caused by a Novel INSR Gene Mutation3
Mild Aromatic L-Amino Acid Decarboxylase Deficiency: As A Reason For Hypoketotic Hypoglycemia In A 4-Year-Old Girl3
Initial Basal and Bolus Rates and Basal Rate Variability During Pump Treatment in Children and Adolescents3
An Unusual Presentation of Carney Complex3
Epicardial and Perihepatic Fat as Cardiometabolic Risk Predictors in Girls with Turner Syndrome: A Cardiac Magnetic Resonance Study3
Catecholamine-induced Myocarditis in a Child with Pheochromocytoma3
46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report3
Early Onset Diabetes in Two Children due to Progeria, a Monogenic Disease of DNA Repair3
The Unusual Case of Fibroma of Tendon Sheath in a Young Girl with Turner Syndrome Undergoing Growth Hormone Treatment3
Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both <i>NF1</i> and Homozygous <i>RET</i> Proto-oncogen Germ-line Mutations3
Serum Neudesin Levels in Obese Adolescents3
A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in <i>IGSF1</i> Gene3
Evaluation of Glucose Metabolism and Cardiovascular Risk Factors in Prepubertal Girls with Premature Pubarche3
The Effects of Risk Behaviors and Orthorexic Behavior on Glycemic Control in Adolescents with Type 1 Diabetes3
The Effects of Prehospital Care on Outcome in Pediatric Diabetic Ketoacidosis3
Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards3
Bronchial Carcinoid Tumour as a Rare Cause of Cushing’s Syndrome in Children: A Case Report and Review of Literature3
Transforming Growth Factor-β1 and Receptor for Advanced Glycation End Products Gene Expression and Protein Levels in Adolescents with Type 1 Diabetes Mellitus3
Pre-treatment Neutropenia in Children and Adolescents with Autoimmune Hyperthyroidism3
The Results of 16 Years of Iodization: Assessment of Iodine Deficiency Among School-age Children in Antalya, Turkey3
The IGSF1 Deficiency Syndrome May Present with Normal Free T4 Levels, Severe Obesity, or Premature Testicular Growth3
A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant3
Soluble CD40 Ligand Levels in Children with Newly Diagnosed Graves’ Disease3
Left Ventricular Hypertrophy in Patients with X-Linked Hypophosphataemia3
Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey3
0.033693790435791