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Evaluation of cardiac autonomic dysfunctions in children with type 1 diabetes mellitus

BMC pediatrics, 2024-04, Vol.24 (1), p.229-229, Article 229

2024

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The Effects of Emotional Labor and Core-Self Assessments on Constructive Deviant Behavior in Hotel Businesses: The Mediating Role of Staff Empowerment

Ege akademik bakıs, 2023-10, Vol.23 (4), p.543-556

2023

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Children with Hashimoto’s Thyroiditis Have Increased Intestinal Permeability: Results of a Pilot Study

Journal of clinical research in pediatric endocrinology, 2020-09, Vol.12 (3), p.303-307

2020

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Evaluation of Unfavorable Cardiovascular and Metabolic Risk Factors in Children and Young Adults with Haemophilia

Journal of clinical research in pediatric endocrinology, 2019-06, Vol.11 (2), p.173-180

2019

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Endocrinological Evaluations of a Neurofibromatosis Type 1 Cohort: Is it Necessary to Evaluate Autoimmune Thyroiditis in Neurofibromatosis Type 1?

Balkan medical journal, 2017-12, Vol.34 (6), p.522-526

2017

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Prenatal androgens and autistic, attention deficit hyperactivity disorder, and disruptive behavior disorders traits

Anadolu psikiyatri dergisi, 2020-08, Vol.21 (4), p.435-442

2020

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Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

Journal of clinical research in pediatric endocrinology, 2019-06, Vol.11 (2), p.164-172

2019

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The Course of COVID-19 in a Patient with Congenital Neutropenia: A Case Report

Bagcilar Medical Bulletin, 2023-03, Vol.8 (1), p.94-98

2023

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Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report

Journal of clinical research in pediatric endocrinology, 2018-12, Vol.10 (4), p.391-394

2018

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The factors relevant to partial remission in children with type 1 diabetes mellitus after measles vaccination: A retrospective study

Journal of medical virology, 2020-12, Vol.92 (12), p.2955-2960

2020

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A novel graphene oxide‐based fluorescence method for detection of urine glycosaminoglycans

Biotechnology and applied biochemistry, 2024-06, Vol.71 (3), p.651-660

2024

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İçecek Tadım Uzmanlarının Bahşiş Davranışına Yönelik Tutumları

Igdır University journal of social sciences, 2023-05 (33), p.147-162

2023

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Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes

Clinical neurology and neurosurgery, 2024-01, Vol.236, p.107893-107893, Article 107893

2024

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A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy

Clinical neurology and neurosurgery, 2023-06, Vol.229, p.107712, Article 107712

2023

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Investigation of (Epi)genetic causes in syndromic short children born small for gestational age

European journal of medical genetics, 2023-11, Vol.66 (11), p.104854-104854, Article 104854

2023

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Differences in the gut microbiota of healthy children and those with type 1 diabetes

Pediatrics international, 2014-06, Vol.56 (3), p.336-343

2014

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A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment

Journal of clinical research in pediatric endocrinology, 2023-10

2023

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Possible genotype-phenotype correlations in Niemann-Pick type C patients and miglustat treatment

Ideggyógyászati szemle, 2021-03, Vol.74 (3-4), p.139

2021

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Novel variants in Turkish patients with glycogen storage disease

Pediatrics international, 2020-10, Vol.62 (10), p.1145-1150

2020

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Treatment of COVID-19 patients with quercetin: a prospective, single center, randomized, controlled trial

Turkish journal of biology, 2021-01, Vol.45 (SI-1), p.518-529

2021

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Treatment of ichthyosis and hypernatremia in a patient with Netherton syndrome with a SPINK5 c.153delT mutation using kallikrein inhibiting ointment

International journal of dermatology, 2017-01, Vol.56 (1), p.106-108

2017

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A Field Study to Determine Organizational Commitment and Job Satisfaction in Hotel Businesses

Revista Latino-Americana de Turismologia, 2020-12

2020

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Recognizing the psychosocial aspects of type 1 diabetes in adolescents

Journal of clinical research in pediatric endocrinology, 2015-03, Vol.7 (1), p.57-62

2015

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A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: Functional analysis of the mutant protein

Molecular genetics and metabolism, 2014-05, Vol.112 (1), p.25-29

2014

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Evaluation of cardiac autonomic dysfunctions in children with type 1 diabetes mellitus

The Effects of Emotional Labor and Core-Self Assessments on Constructive Deviant Behavior in Hotel Businesses: The Mediating Role of Staff Empowerment

Children with Hashimoto’s Thyroiditis Have Increased Intestinal Permeability: Results of a Pilot Study

Evaluation of Unfavorable Cardiovascular and Metabolic Risk Factors in Children and Young Adults with Haemophilia

Endocrinological Evaluations of a Neurofibromatosis Type 1 Cohort: Is it Necessary to Evaluate Autoimmune Thyroiditis in Neurofibromatosis Type 1?

Prenatal androgens and autistic, attention deficit hyperactivity disorder, and disruptive behavior disorders traits

Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience

The Course of COVID-19 in a Patient with Congenital Neutropenia: A Case Report

Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report

The factors relevant to partial remission in children with type 1 diabetes mellitus after measles vaccination: A retrospective study

A novel graphene oxide‐based fluorescence method for detection of urine glycosaminoglycans

İçecek Tadım Uzmanlarının Bahşiş Davranışına Yönelik Tutumları

Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes

A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy

Investigation of (Epi)genetic causes in syndromic short children born small for gestational age

Differences in the gut microbiota of healthy children and those with type 1 diabetes

A Rare Case of Monogenic Obesity due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment

Possible genotype-phenotype correlations in Niemann-Pick type C patients and miglustat treatment

Novel variants in Turkish patients with glycogen storage disease

Treatment of COVID-19 patients with quercetin: a prospective, single center, randomized, controlled trial

Treatment of ichthyosis and hypernatremia in a patient with Netherton syndrome with a SPINK5 c.153delT mutation using kallikrein inhibiting ointment

A Field Study to Determine Organizational Commitment and Job Satisfaction in Hotel Businesses

Recognizing the psychosocial aspects of type 1 diabetes in adolescents

The frequency of and factors affecting functional gastrointestinal disorders in infants that presented to tertiary care hospitals

A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: Functional analysis of the mutant protein

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