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Cardiovascular Risk Factors in Adolescents with Type 1 Diabetes: Prevalence and Gender Differences

Journal of clinical research in pediatric endocrinology, 2024-03, Vol.16 (1), p.11-20

2024

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Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose?

Journal of clinical research in pediatric endocrinology, 2020-03, Vol.12 (1), p.37-44

2020

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Membranoproliferative glomerulonephritis in a patient with lysinuric protein intolerance: lesson for the clinical nephrologist

Journal of nephrology, 2024-07

2024

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Hyperinsulinism may be Underreported in Hypoglycemic Patients with Phosphomannomutase 2 Deficiency

Journal of clinical research in pediatric endocrinology, 2022-09, Vol.14 (3), p.275-286

2022

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Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

Journal of clinical research in pediatric endocrinology, 2021-03, Vol.13 (1), p.34-43

2021

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Feminizing Adrenocortical Tumors as a Rare Etiology of Isosexual/Contrasexual Pseudopuberty

Journal of clinical research in pediatric endocrinology, 2022-03, Vol.14 (1), p.17-28

2022

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Santral puberte prekoks tanısında bazal lütenizan hormon düzeyinin yeterliliği

Turk Pediatri Arsivi, 2019

Vurallı, Doğuş

2019

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Growth Hormone Deficiency in the Transition Period

Turkish journal of endocrinology and metabolism, 2019, Vol.23 (3), p.181-186

VURALLI, Doğuş

2019

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A pheochromocytoma case diagnosed as adrenal incidentaloma

Turkish journal of pediatrics, 2017, Vol.59 (2), p.200-206

2017

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Leukocyte populations and C-reactive protein as predictors of bacterial infections in febrile outpatient children

Turkish journal of haematology, 2014-03, Vol.31 (1), p.49-55

2014

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Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency

Turkish journal of pediatrics, 2012-11, Vol.54 (6), p.570-575

2012

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Gender-related differences in etiology of organic central precocious puberty

Turkish journal of pediatrics, 2020-09, Vol.62 (5), p.763-769

2020

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Clinical Approach to Hypocalcemia in Newborn Period and Infancy: Who Should Be Treated?

International journal of pediatrics, 2019-01, Vol.2019 (2019), p.1-7

2019

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Kawasaki-like disease in children with COVID-19

Rheumatology international, 2020-12, Vol.40 (12), p.2105-2115

2020

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Ion Transporters, Channelopathies, and Glucose Disorders

International journal of molecular sciences, 2019-05, Vol.20 (10), p.2590

2019

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Epidemiology of type 1 diabetes mellitus in children and adolescents: A 50‐year, single‐center experience

Journal of diabetes, 2024-05, Vol.16 (5), p.e13562-n/a

2024

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Zinc deficiency in the pediatric age group is common but underevaluated

World journal of pediatrics : WJP, 2017-08, Vol.13 (4), p.360-366

2017

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Evdeki Yeşil Tehlikeler 'Difenbahya Zehirlenmesi'

Gazi tıp dergisi, 2010-01, Vol.21 (1), p.51-52

2010

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儿童新发1型糖尿病诊断后早期体重增加可能对缓解状态产生影响

Journal of diabetes, 2023-12, Vol.15 (12), p.1011-1019

2023

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Central nervous system imaging in girls with central precocious puberty: when is necessary?

Archives of Endocrinology and Metabolism, 2021-05, Vol.64 (5), p.591-596

2021

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Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1Aand SCNN1BGenes

Hormone research in paediatrics, 2019, Vol.91 (3), p.175-185

2019

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Serum kisspeptin, neurokinin B and inhibin B levels can be used as alternative parameters to distinguish idiopathic CPP from premature thelarche in the early stages of puberty

Clinical endocrinology (Oxford), 2023-06, Vol.98 (6), p.788-795

2023

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Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (3), p.249-252

2015

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Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.96-100

2016

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Surgical and clinical strategies in the management of thyroid medullary carcinoma in children with and without ret proto-oncogene mutations

Turkish journal of pediatrics, 2016, Vol.58 (4), p.436-441

2016

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Cardiovascular Risk Factors in Adolescents with Type 1 Diabetes: Prevalence and Gender Differences

Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose?

Membranoproliferative glomerulonephritis in a patient with lysinuric protein intolerance: lesson for the clinical nephrologist

Hyperinsulinism may be Underreported in Hypoglycemic Patients with Phosphomannomutase 2 Deficiency

Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

Feminizing Adrenocortical Tumors as a Rare Etiology of Isosexual/Contrasexual Pseudopuberty

Santral puberte prekoks tanısında bazal lütenizan hormon düzeyinin yeterliliği

Growth Hormone Deficiency in the Transition Period

A pheochromocytoma case diagnosed as adrenal incidentaloma

Leukocyte populations and C-reactive protein as predictors of bacterial infections in febrile outpatient children

Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency

Gender-related differences in etiology of organic central precocious puberty

Clinical Approach to Hypocalcemia in Newborn Period and Infancy: Who Should Be Treated?

Kawasaki-like disease in children with COVID-19

Ion Transporters, Channelopathies, and Glucose Disorders

Epidemiology of type 1 diabetes mellitus in children and adolescents: A 50‐year, single‐center experience

Zinc deficiency in the pediatric age group is common but underevaluated

Evdeki Yeşil Tehlikeler 'Difenbahya Zehirlenmesi'

儿童新发1型糖尿病诊断后早期体重增加可能对缓解状态产生影响

Central nervous system imaging in girls with central precocious puberty: when is necessary?

Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1Aand SCNN1BGenes

Serum kisspeptin, neurokinin B and inhibin B levels can be used as alternative parameters to distinguish idiopathic CPP from premature thelarche in the early stages of puberty

Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome

Surgical and clinical strategies in the management of thyroid medullary carcinoma in children with and without ret proto-oncogene mutations

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