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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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Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature

Journal of clinical research in pediatric endocrinology, 2020-11, Vol.12 (4), p.358-365

2020

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Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings

The journal of pediatric research, 2020-12, Vol.7 (4), p.267-272

2020

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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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A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia

Journal of clinical research in pediatric endocrinology, 2020-03, Vol.12 (1), p.113-116

2020

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A case of Williams syndrome with Wolff–Parkinson–White syndrome

Birth defects research, 2024-07, Vol.116 (7), p.e2385-n/a

2024

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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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Investigation of miRNA and cytokine expressions in latent tuberculosis infection and active tuberculosis

Turkish journal of medical sciences, 2022-01, Vol.52 (3), p.649-657

2022

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The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals

Biology of sport, 2019-01, Vol.36 (1), p.9-16

2019

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MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Balkan medical journal, 2018-03, Vol.35 (2), p.163-166

2018

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Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Balkan medical journal, 2018-03, Vol.35 (2), p.163-166

2018

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Genetic Counseling in Neurofibromatosis Type 1

The journal of pediatric research, 2014-09, Vol.1 (3), p.152-154

2014

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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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Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages

Scandinavian journal of immunology, 2019-02, Vol.89 (2), p.e12737-n/a

2019

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The Evaluation of Epidemiological and Clinical Findings of 33 Children Observed with Henoch Schönlein Purpura

The journal of pediatric research, 2014-12, Vol.1 (4), p.199-202

2014

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The Impact of e-Health Literacy on Health Promotion Behaviors of High School Students

The journal of pediatric research, 2020-12, Vol.7 (4), p.286-292

2020

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The association between genetic polymorphisms in matrix metalloproteinases and caries experience

Clinical oral investigations, 2021-09, Vol.25 (9), p.5403-5410

2021

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UroVysion Fluorescence in situ hybridization (UroVysion FISH) assay for detecting Turkish bladder cancer patients in voided urine: A preliminary study

Contemporary oncology (Poznań, Poland), 2013-03, Vol.17 (2), p.156

2013

Volltextzugriff (PDF)

The Effect of Web-based Diabetes Education on the Metabolic Control, Self-efficacy and Quality of Life of Adolescents with Type 1 Diabetes Mellitus in Turkey

The journal of pediatric research, 2021-06, Vol.8 (2), p.131-138

2021

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The Relation of Complete Blood Count Parameters with Metabolic and Clinical Parameters in Overweight and Obese Children

The journal of pediatric research, 2021-06, Vol.8 (2), p.161-170

2021

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A Unique Case of Thrombophilia: The Role of F9 Gene Duplication and Increased FIX Activity in Cerebral Venous Thrombosis

Journal of thrombosis and haemostasis, 2023-07

2023

Volltextzugriff (PDF)

The Prevalence of Sports-related Dental Injuries and the Rate of Awareness of Mouthguard Use among Child Athletes

The journal of pediatric research, 2020-12, Vol.7 (4), p.358-364

2020

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Childhood Asthma and Vitamin D-case Control Study in an Academic Tertiary Care Hospital

The journal of pediatric research, 2021-06, Vol.8 (2), p.188-194

2021

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Comparison of the Efficacy of Three Natural Surfactants in Preterm Turkish Newborns with Respiratory Distress Syndrome

The journal of pediatric research, 2021-06, Vol.8 (2), p.124-130

2021

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Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation

Journal of clinical research in pediatric endocrinology, 2024-06

2024

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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

Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature

Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings

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

A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia

A case of Williams syndrome with Wolff–Parkinson–White syndrome

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

Investigation of miRNA and cytokine expressions in latent tuberculosis infection and active tuberculosis

The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals

MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome

Genetic Counseling in Neurofibromatosis Type 1

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

Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages

The Evaluation of Epidemiological and Clinical Findings of 33 Children Observed with Henoch Schönlein Purpura

The Impact of e-Health Literacy on Health Promotion Behaviors of High School Students

The association between genetic polymorphisms in matrix metalloproteinases and caries experience

UroVysion Fluorescence in situ hybridization (UroVysion FISH) assay for detecting Turkish bladder cancer patients in voided urine: A preliminary study

The Effect of Web-based Diabetes Education on the Metabolic Control, Self-efficacy and Quality of Life of Adolescents with Type 1 Diabetes Mellitus in Turkey

The Relation of Complete Blood Count Parameters with Metabolic and Clinical Parameters in Overweight and Obese Children

A Unique Case of Thrombophilia: The Role of F9 Gene Duplication and Increased FIX Activity in Cerebral Venous Thrombosis

The Prevalence of Sports-related Dental Injuries and the Rate of Awareness of Mouthguard Use among Child Athletes

Childhood Asthma and Vitamin D-case Control Study in an Academic Tertiary Care Hospital

Comparison of the Efficacy of Three Natural Surfactants in Preterm Turkish Newborns with Respiratory Distress Syndrome

Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation

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