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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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3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience

European journal of medical genetics, 2023-10, Vol.66 (10), p.104828-104828, Article 104828

2023

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Early visual field changes in patients with type 1 diabetes mellitus

European journal of ophthalmology, 2020-11, Vol.30 (6), p.1467-1472

2020

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Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets

Journal of pediatric endocrinology & metabolism : JPEM, 2015-11, Vol.28 (11-12), p.1333

2015

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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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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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Decreased vitamin D levels in children and adolescents with Celiac disease: A nationwide cross-sectional study

Gülhane tıp dergisi, 2022-09, Vol.64 (3), p.268-273

2022

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A major health problem facing immigrant children: nutritional rickets

Journal of pediatric endocrinology & metabolism : JPEM, 2022-02, Vol.35 (2), p.223

2022

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A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make

Journal of clinical research in pediatric endocrinology, 2018-03, Vol.10 (1), p.68-73

2018

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Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

European journal of medical genetics, 2022-12, Vol.65 (12), p.104654-104654, Article 104654

2022

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Comparison of Anterior Segment Parameters in Juvenile Diabetes Mellitus and Healthy Eyes

European journal of ophthalmology, 2016-11, Vol.26 (6), p.618-622

2016

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Low hemoglobin A1c levels in a patient with diabetic ketoacidosis: Fulminant type 1 diabetes mellitus

Turkish journal of pediatrics, 2018, Vol.60 (2), p.201-205

2018

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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 & metabolism : JPEM, 2019-06, Vol.32 (6), p.647

2019

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A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

Journal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.91-94

2017

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Congenital long-QT syndrome in type 1 diabetes: a unique association

Turkish journal of pediatrics, 2019, Vol.61 (5), p.791-793

2019

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Optic Nerve Parameters in Obese Children as Measured by Spectral Domain Optical Coherence Tomography

Seminars in ophthalmology, 2017-11, Vol.32 (6), p.743-747

2017

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The evaluation of transient hypothyroidism in patients diagnosed with congenital hypothyroidism

Turkish journal of medical sciences, 2015-01, Vol.45 (4), p.745-750

2015

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Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report

Turkish journal of pediatrics, 2016-11, Vol.58 (6), p.654-657

2016

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A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood

Turkish journal of pediatrics, 2016, Vol.58 (4), p.446-451

2016

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Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis

Turkish journal of pediatrics, 2016, Vol.58 (5), p.538-540

2016

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The first childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis

Turkish journal of pediatrics, 2016, Vol.58 (4), p.432-435

2016

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Evaluation of Thiol/Disulfide Homeostasis in Pediatric Patients with Diabetic Ketoacidosis

Combinatorial chemistry & high throughput screening, 2020-01, Vol.23 (3), p.185

2020

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Clinical and Laboratory Characteristics of MODY (Maturity Onset Diabetes of Young) Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship

Journal of clinical research in pediatric endocrinology, 2024-04

2024

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Early Ophthalmic Artery Blood Flow Parameter Changes in Patients with Type 1 Diabetes Mellitus

Beyoglu eye journal, 2020, Vol.5 (1), p.17-21

2020

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17α-Hydroylase/17,20-lyase deficiency related to P.Y27(c.81C>A) mutation in CYP17A1 gene

Journal of pediatric endocrinology & metabolism : JPEM, 2015-07, Vol.28 (7-8), p.919

2015

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

3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience

Early visual field changes in patients with type 1 diabetes mellitus

Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets

Antimüllerian Hormone Levels of Infants with Premature Thelarche

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

Decreased vitamin D levels in children and adolescents with Celiac disease: A nationwide cross-sectional study

A major health problem facing immigrant children: nutritional rickets

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make

Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

Comparison of Anterior Segment Parameters in Juvenile Diabetes Mellitus and Healthy Eyes

Low hemoglobin A1c levels in a patient with diabetic ketoacidosis: Fulminant type 1 diabetes mellitus

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

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

Congenital long-QT syndrome in type 1 diabetes: a unique association

Optic Nerve Parameters in Obese Children as Measured by Spectral Domain Optical Coherence Tomography

The evaluation of transient hypothyroidism in patients diagnosed with congenital hypothyroidism

Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report

A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood

Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis

The first childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis

Evaluation of Thiol/Disulfide Homeostasis in Pediatric Patients with Diabetic Ketoacidosis

Clinical and Laboratory Characteristics of MODY (Maturity Onset Diabetes of Young) Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship

Early Ophthalmic Artery Blood Flow Parameter Changes in Patients with Type 1 Diabetes Mellitus

17α-Hydroylase/17,20-lyase deficiency related to P.Y27(c.81C>A) mutation in CYP17A1 gene

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