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Incidence of type 1 diabetes mellitus in Turkish children from the southeastern region of the country: a regional report

Journal of clinical research in pediatric endocrinology, 2013-01, Vol.5 (2), p.98-103

2013

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Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-eastern Region of Turkey

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.295-302

2020

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Restless Legs Syndrome and Poor Sleep Quality in Obese Children and Adolescents

Journal of clinical research in pediatric endocrinology, 2018-06, Vol.10 (2), p.131-138

2018

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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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Multiple pituitary hormone deficiency due to gunshot injury in a 6-year-old girl

Journal of clinical research in pediatric endocrinology, 2013-09, Vol.5 (3), p.209-211

2013

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Obez çocuk ve adolesanlarda vücut kitle indeksi ve biyoelektrik impedans yöntemi ile ölçülen vücut yağ oranının lipid düzeyleri ve metabolik parametrelerle ilişkisi

Pamukkale Medical Journal, 2018-09

Baran, Rıza Taner

2018

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A novel diagnostic tool for the evaluation of hypothalamic-pituitary region and diagnosis of growth hormone deficiency: pons ratio

Journal of Pediatric Endocrinology and Metabolism, 2020-05, Vol.33 (6), p.735-742

2020

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Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-e4359

2020

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Assessing adolescent gynecomastia: The role of shear wave ultrasound elastography

Journal of clinical ultrasound, 2024-09

2024

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Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I

Hormone research in paediatrics, 2016-01, Vol.85 (5), p.309-317

2016

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Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations

European journal of endocrinology, 2015-06, Vol.172 (6), p.697-705

2015

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Evaluation of Turkish pediatric voice handicap index in children with asthma

Annals of Clinical and Analytical Medicine, 2020-03, Vol.11 (2)

2020

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Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia

The journal of clinical endocrinology and metabolism, 2014-12, Vol.99 (12), p.E2730-E2734

2014

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Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.163-169

2016

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Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations

European journal of endocrinology, 2014-06, Vol.170 (6), p.885-892

2014

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Restless legs syndrome in children with allergic rhinitis: A comparative study on frequency, severity and sleep quality

Turkish journal of physical medicine and rehabilitation, 2018-09, Vol.64 (3), p.198

2018

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A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency

Journal of Pediatric Endocrinology and Metabolism, 2021-11, Vol.34 (11), p.1463-1468

2021

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Evaluation of Pediatric Voice Handicap Index in Children With Allergic Rhinitis

Journal of voice, 2019-09, Vol.33 (5), p.801.e17-801.e20

2019

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Çocukluk çağında nadir görülen idiyopatik hipoparatiroidizm ve bazal gangliyon kalsifikasyonu birlikteliği: Fahr hastalığı

Cukurova Medical Journal, 2018-03, Vol.43 (1), p.231-234

2018

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Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions

Turkish journal of pediatrics, 2018, Vol.60 (5), p.554-561

2018

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Mutations in BTD gene causing biotinidase deficiency: a regional report

Journal of Pediatric Endocrinology and Metabolism, 2015-03, Vol.28 (3-4), p.421

2015

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Restless legs syndrome in children with allergic rhinitis: A comparative study on frequency, severity and sleep quality

Turkish journal of physical medicine and rehabilitation, 2018-09, Vol.64 (3), p.198-204

Bilgilisoy Filiz, Meral

2018

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Prepubertal unilateral gynecomastia: report of 2 cases

Journal of clinical research in pediatric endocrinology, 2014-12, Vol.6 (4), p.250-253

2014

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Santral Tiroid Hormon Direnci Saptanan Olgularda Tiroid Hormon Reseptör Gen Analizi ve Periferik Direnç Eşliğinin Araştırılması

Turkish Journal of Pediatric Disease, 2020-01, p.1-8

2020

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Incidence of type 1 diabetes mellitus in Turkish children from the southeastern region of the country: a regional report

Evaluation of the Final Adult Height and Its Determinants in Patients with Growth Hormone Deficiency: A Single-centre Experience from the South-eastern Region of Turkey

Restless Legs Syndrome and Poor Sleep Quality in Obese Children and Adolescents

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

Multiple pituitary hormone deficiency due to gunshot injury in a 6-year-old girl

Obez çocuk ve adolesanlarda vücut kitle indeksi ve biyoelektrik impedans yöntemi ile ölçülen vücut yağ oranının lipid düzeyleri ve metabolik parametrelerle ilişkisi

A novel diagnostic tool for the evaluation of hypothalamic-pituitary region and diagnosis of growth hormone deficiency: pons ratio

Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations

Assessing adolescent gynecomastia: The role of shear wave ultrasound elastography

Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations

Evaluation of Turkish pediatric voice handicap index in children with asthma

Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations

Restless legs syndrome in children with allergic rhinitis: A comparative study on frequency, severity and sleep quality

A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency

Evaluation of Pediatric Voice Handicap Index in Children With Allergic Rhinitis

Çocukluk çağında nadir görülen idiyopatik hipoparatiroidizm ve bazal gangliyon kalsifikasyonu birlikteliği: Fahr hastalığı

Evaluation of psychological characteristics of Turkish children with type 1 diabetes mellitus from two demographically and geographically distinct regions

Mutations in BTD gene causing biotinidase deficiency: a regional report

Restless legs syndrome in children with allergic rhinitis: A comparative study on frequency, severity and sleep quality

Prepubertal unilateral gynecomastia: report of 2 cases

Santral Tiroid Hormon Direnci Saptanan Olgularda Tiroid Hormon Reseptör Gen Analizi ve Periferik Direnç Eşliğinin Araştırılması

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