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The Relationship Between Premature Adrenarche and Markers of Inflammation in Complete Blood Count

The journal of pediatric research, 2024-03, Vol.11 (1), p.52-57

2024

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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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Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies

Case Reports in Immunology, 2017-01, Vol.2017 (2017), p.1-6

2017

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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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Evaluation of the Relationship Between Peak Growth Hormone Response to Growth Hormone Stimulation Tests and Body Mass Index

Medical Science and Discovery, 2023-10, Vol.10 (10), p.779-783

2023

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Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta

Journal of Pediatric Endocrinology and Metabolism, 2024-08, Vol.37 (8), p.693-700

2024

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Predicting diabetic kidney disease in youth with type 1 diabetes: Insights from genetic risk assessment

Journal of diabetes and its complications, 2024-11, Vol.38 (11), p.108833, Article 108833

2024

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Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene

Diabetes research and clinical practice, 2023-11, Vol.205, p.110953-110953, Article 110953

2023

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Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition

Journal of Pediatric Endocrinology and Metabolism, 2023-01, Vol.36 (1), p.64-73

2023

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A case-control study of early-stage radiological markers of endothelial dysfunction and cardiovascular findings in patients with osteogenesis imperfecta: genotype–phenotype correlations

Journal of Pediatric Endocrinology and Metabolism, 2023-12, Vol.36 (12), p.1161-1168

2023

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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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ABCC8-related maturity-onset diabetes of the young: switching from insulin to sulphonylurea therapy: how long do we need for a good metabolic control?

Journal of Pediatric Endocrinology and Metabolism, 2023-06

2023

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Basal and Bolus Insulin Distribution According to Treatment Modality: Data from SWEET Diabetes Registry

Pediatric diabetes, 2023-08, Vol.2023, p.1-8

2023

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Glycated hemoglobin variability and microvascular complications in patients with type 1 diabetes mellitus

Journal of Pediatric Endocrinology and Metabolism, 2020-12, Vol.33 (12), p.1533-1537

2020

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Treatment and long-term follow-up of patients diagnosed with type 1 diabetes mellitus before age 5

Journal of Pediatric Endocrinology and Metabolism, 2021-02, Vol.34 (2), p.201-207

2021

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Juvenile Dermatomyositis with a Rare and Severe Complication: Macrophage Activation Syndrome

The journal of pediatric research, 2014-12, Vol.1 (4), p.218-221

2014

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Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies

Case reports in immunology, 2017, Vol.2017, p.2846928-2846928

2017

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The Relationship Between Premature Adrenarche and Markers of Inflammation in Complete Blood Count

Predictive low-glucose suspend system and glycemic variability

Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies

Prediction of Transient or Permanent Congenital Hypothyroidism

Evaluation of the Relationship Between Peak Growth Hormone Response to Growth Hormone Stimulation Tests and Body Mass Index

Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta

Predicting diabetic kidney disease in youth with type 1 diabetes: Insights from genetic risk assessment

Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene

Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition

A case-control study of early-stage radiological markers of endothelial dysfunction and cardiovascular findings in patients with osteogenesis imperfecta: genotype–phenotype correlations

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

ABCC8-related maturity-onset diabetes of the young: switching from insulin to sulphonylurea therapy: how long do we need for a good metabolic control?

Basal and Bolus Insulin Distribution According to Treatment Modality: Data from SWEET Diabetes Registry

Glycated hemoglobin variability and microvascular complications in patients with type 1 diabetes mellitus

Treatment and long-term follow-up of patients diagnosed with type 1 diabetes mellitus before age 5

Juvenile Dermatomyositis with a Rare and Severe Complication: Macrophage Activation Syndrome

Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies

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