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Melanocortin 4 receptor (MC4R) gene variants in children and adolescents having familial early-onset obesity: genetic and clinical characteristics

European journal of pediatrics, 2020-09, Vol.179 (9), p.1445-1452

2020

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A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism

Journal of clinical research in pediatric endocrinology, 2021-03, Vol.13 (1), p.52-60

2021

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Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis

Archives of Endocrinology and Metabolism, 2024-01, Vol.68, p.e220475

2024

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Novel Modified Algorithm for High Fat/High Energy Density Meal in Type 1 Diabetes: Less Hypoglycemia

Journal of clinical research in pediatric endocrinology, 2023-06, Vol.15 (2), p.138-144

2023

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The psychosocial outcomes of advanced hybrid closed-loop system in children and adolescents with type 1 diabetes

European journal of pediatrics, 2024-07, Vol.183 (7), p.3095-3103

2024

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The Effect of the SARS-CoV-2 Pandemic on Presentation with Diabetic Ketoacidosis in Children with New Onset Type 1 Diabetes Mellitus

Journal of clinical research in pediatric endocrinology, 2023-09, Vol.15 (3), p.264-267

2023

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Insulin pump therapy in children with type 1 diabetes: analysis of data from the SWEET registry

Pediatric diabetes, 2016-10, Vol.17 (S23), p.38-45

2016

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Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene

Journal of clinical research in pediatric endocrinology, 2020-03, Vol.12 (1), p.109-112

2020

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The Effects of Prehospital Care on Outcome in Pediatric Diabetic Ketoacidosis

Journal of clinical research in pediatric endocrinology, 2020-06, Vol.12 (2), p.189-196

2020

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Effect of metabolic control on cognitive functions in children and adolescents with type 1 diabetes mellitus

Journal of pediatric endocrinology & metabolism : JPEM, 2023-07, Vol.36 (7), p.636

2023

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Initial Basal and Bolus Rates and Basal Rate Variability During Pump Treatment in Children and Adolescents

Journal of clinical research in pediatric endocrinology, 2021-06, Vol.13 (2), p.198-203

2021

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A large cohort of disorders of sex development and their genetic characteristics: 6 novel mutations in known genes

European journal of medical genetics, 2021-03, Vol.64 (3), p.104154-104154, Article 104154

2021

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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 Cases

Journal of clinical research in pediatric endocrinology, 2021-12, Vol.13 (4), p.468-472

2021

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Reliability and Validity of the Diabetes Eating Problem Survey in Turkish Children and Adolescents with Type 1 Diabetes Mellitus

Journal of clinical research in pediatric endocrinology, 2017-12, Vol.9 (4), p.323-328

2017

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Adherence to growth hormone therapy: results of a multicenter study

Endocrine practice, 2014-01, Vol.20 (1), p.46-51

2014

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Effect of Education on Impaired Hypoglycemia Awareness and Glycemic Variability in Children and Adolescents with Type 1 Diabetes Mellitus

Journal of clinical research in pediatric endocrinology, 2019-06, Vol.11 (2), p.189-195

2019

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Predictive low-glucose suspend system and glycemic variability

International journal of diabetes in developing countries, 2022-04, Vol.42 (2), p.276-282

2022

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Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development

Journal of clinical research in pediatric endocrinology, 2021-03, Vol.13 (1), p.23-33

2021

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Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

Journal of clinical research in pediatric endocrinology, 2021-09, Vol.13 (3), p.308-319

2021

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Rapid Molecular Genetic Diagnosis with Next-Generation Sequencing in 46,XY Disorders of Sex Development Cases: Efficiency and Cost Assessment

Hormone research in paediatrics, 2017-01, Vol.87 (2), p.81-87

2017

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Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

Journal of clinical research in pediatric endocrinology, 2021-12, Vol.13 (4), p.433-438

2021

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Psychiatric view for disorders of sex development: a 12-year experience of a multidisciplinary team in a university hospital

Journal of pediatric endocrinology & metabolism : JPEM, 2020-05, Vol.33 (5), p.605

2020

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Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

Journal of clinical research in pediatric endocrinology, 2020-06, Vol.12 (2), p.150-159

2020

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Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations

Gene, 2018-01, Vol.641, p.186-189

2018

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Prediction of Transient or Permanent Congenital Hypothyroidism

The journal of pediatric research, 2022-03, Vol.9 (1), p.38-45

2022

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Melanocortin 4 receptor (MC4R) gene variants in children and adolescents having familial early-onset obesity: genetic and clinical characteristics

A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism

Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis

Novel Modified Algorithm for High Fat/High Energy Density Meal in Type 1 Diabetes: Less Hypoglycemia

The psychosocial outcomes of advanced hybrid closed-loop system in children and adolescents with type 1 diabetes

The Effect of the SARS-CoV-2 Pandemic on Presentation with Diabetic Ketoacidosis in Children with New Onset Type 1 Diabetes Mellitus

Insulin pump therapy in children with type 1 diabetes: analysis of data from the SWEET registry

Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene

The Effects of Prehospital Care on Outcome in Pediatric Diabetic Ketoacidosis

Effect of metabolic control on cognitive functions in children and adolescents with type 1 diabetes mellitus

Initial Basal and Bolus Rates and Basal Rate Variability During Pump Treatment in Children and Adolescents

A large cohort of disorders of sex development and their genetic characteristics: 6 novel mutations in known genes

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 Cases

Reliability and Validity of the Diabetes Eating Problem Survey in Turkish Children and Adolescents with Type 1 Diabetes Mellitus

Adherence to growth hormone therapy: results of a multicenter study

Effect of Education on Impaired Hypoglycemia Awareness and Glycemic Variability in Children and Adolescents with Type 1 Diabetes Mellitus

Predictive low-glucose suspend system and glycemic variability

Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

Rapid Molecular Genetic Diagnosis with Next-Generation Sequencing in 46,XY Disorders of Sex Development Cases: Efficiency and Cost Assessment

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

Psychiatric view for disorders of sex development: a 12-year experience of a multidisciplinary team in a university hospital

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations

Prediction of Transient or Permanent Congenital Hypothyroidism

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