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Temporary Thyroid Dysfunction and Catecholamine Excess Due to Mercury Poisoning in 6 Cases

Turkish Archives of Pediatrics, 2024-01, Vol.59 (1), p.23-30

2024

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The association between vitamin D levels and the clinical severity and inflammation markers in pediatric COVID-19 patients: single-center experience from a pandemic hospital

European journal of pediatrics, 2021-08, Vol.180 (8), p.2699-2705

2021

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Evaluation of long-term follow-up and methimazole therapy outcomes of pediatric Graves' disease: a single-center experience

Journal of Pediatric Endocrinology and Metabolism, 2019-04, Vol.32 (4), p.341-346

2019

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The potential of the Mediterranean diet to improve metabolic control and body composition in youths with Type 1 Diabetes Mellitus

BMC endocrine disorders, 2024-05, Vol.24 (1), p.63-63, Article 63

2024

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Evaluation of the pathophysiological role of Fetuin A levels in adolescents with polycystic ovary syndrome

Journal of Pediatric Endocrinology and Metabolism, 2021-07, Vol.34 (7), p.911-916

2021

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Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal‐recessive hypophosphataemic rickets type 2

Clinical endocrinology (Oxford), 2024-11, Vol.101 (5), p.475-484

2024

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Serum Fetuin-A and Insulin Levels in Classic Congenital Adrenal Hyperplasia

Hormone and metabolic research, 2020-09, Vol.52 (9), p.654-659

2020

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Long-term follow-up data of patients with Multiple Pituitary Hormone Deficiency

Andes pediatrica : revista Chilena de pediatría, 2023-12, Vol.94 (6), p.689-697

2023

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Seguimiento a largo plazo de pacientes con Deficiencia Hormonal Hipofisiaria Múltiple

Andes pediatrica : revista Chilena de pediatría, 2023-12, Vol.94 (6), p.689-697

2023

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Pteridine and tryptophan pathways in children with type 1 diabetes: Isoxanthopterin as an indicator of endothelial dysfunction

Journal of pharmaceutical and biomedical analysis, 2024-06, Vol.243, p.116072-116072, Article 116072

2024

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Authors’ reply: the biologic importance of the vitamin D binding protein polymorphism in pediatric COVID-19 patients

European journal of pediatrics, 2021-08, Vol.180 (8), p.2709-2710

2021

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Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia

Journal of clinical research in pediatric endocrinology, 2021-09, Vol.13 (3), p.300-307

2021

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Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis

Familial cancer, 2023-10, Vol.22 (4), p.487-493

2023

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Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation

Journal of Pediatric Endocrinology and Metabolism, 2019-06, Vol.32 (6), p.647-651

2019

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Clitoromegaly caused by ovarian stimulation in a preterm newborn: ovarian hyperstimulation syndrome of preterm babies

Turkish journal of pediatrics, 2020-11, Vol.62 (6), p.1088-1093

2020

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Clinical and genetic characterisation of a series of patients with triple A syndrome

European journal of pediatrics, 2018-03, Vol.177 (3), p.363-369

2018

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Effects of 1-year growth hormone replacement therapy on thyroid volume and function of the children and adolescents with idiopathic growth hormone deficiency

Journal of Pediatric Endocrinology and Metabolism, 2017-10, Vol.30 (11), p.1187

2017

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Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

Journal of clinical research in pediatric endocrinology, 2018-09, Vol.10 (3), p.223-229

2018

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Vaginal bleeding and a giant ovarian cyst in an infant with 21-hydroxylase deficiency

Journal of Pediatric Endocrinology and Metabolism, 2018-02, Vol.31 (2), p.229-233

2018

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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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Antimüllerian Hormone Levels of Infants with Premature Thelarche

Journal of clinical research in pediatric endocrinology, 2019-09, Vol.11 (3), p.287-292

2019

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EVALUATION OF FINAL HEIGHT IN PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA

Pamukkale Medical Journal, 2024-01

2024

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Objective Evaluation of Corneal and Lens Clarity in Children with Type 1 Diabetes Mellitus

American journal of ophthalmology, 2017-07, Vol.179, p.190-197

2017

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SARS-COV-2 infections in children: The role of fibrinogen in predicting diagnosis and severity: A retrospective cohort study

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2024-01, Vol.33 (1), p.31-38

2024

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Quantitative evaluation of early retinal changes in children with type 1 diabetes mellitus without retinopathy

Clinical and experimental optometry, 2018-09, Vol.101 (5), p.680-685

2018

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Temporary Thyroid Dysfunction and Catecholamine Excess Due to Mercury Poisoning in 6 Cases

The association between vitamin D levels and the clinical severity and inflammation markers in pediatric COVID-19 patients: single-center experience from a pandemic hospital

Evaluation of long-term follow-up and methimazole therapy outcomes of pediatric Graves' disease: a single-center experience

The potential of the Mediterranean diet to improve metabolic control and body composition in youths with Type 1 Diabetes Mellitus

Evaluation of the pathophysiological role of Fetuin A levels in adolescents with polycystic ovary syndrome

Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal‐recessive hypophosphataemic rickets type 2

Serum Fetuin-A and Insulin Levels in Classic Congenital Adrenal Hyperplasia

Long-term follow-up data of patients with Multiple Pituitary Hormone Deficiency

Seguimiento a largo plazo de pacientes con Deficiencia Hormonal Hipofisiaria Múltiple

Pteridine and tryptophan pathways in children with type 1 diabetes: Isoxanthopterin as an indicator of endothelial dysfunction

Authors’ reply: the biologic importance of the vitamin D binding protein polymorphism in pediatric COVID-19 patients

Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia

Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis

Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation

Clitoromegaly caused by ovarian stimulation in a preterm newborn: ovarian hyperstimulation syndrome of preterm babies

Clinical and genetic characterisation of a series of patients with triple A syndrome

Effects of 1-year growth hormone replacement therapy on thyroid volume and function of the children and adolescents with idiopathic growth hormone deficiency

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

Vaginal bleeding and a giant ovarian cyst in an infant with 21-hydroxylase deficiency

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

Antimüllerian Hormone Levels of Infants with Premature Thelarche

EVALUATION OF FINAL HEIGHT IN PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA

Objective Evaluation of Corneal and Lens Clarity in Children with Type 1 Diabetes Mellitus

SARS-COV-2 infections in children: The role of fibrinogen in predicting diagnosis and severity: A retrospective cohort study

Quantitative evaluation of early retinal changes in children with type 1 diabetes mellitus without retinopathy

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