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The Evaluation of the Genetic Variation Types of the Uridine Diphosphate Glucuronosyl Transferase 1A1 Gene by Next-Generation Sequencing and Their Effects on Bilirubin Levels in Obese Children

Genetic testing and molecular biomarkers, 2024-07, Vol.28 (7), p.275-280

2024

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Does capsaicin have therapeutic benefits in human colon adenocarcinoma? Selection of the most reliable dose via AgNOR

TURKISH JOURNAL OF MEDICAL SCIENCES, 2020-06, Vol.50 (4), p.1076-1081

2020

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Argyrophilic Nucleolar Organizer Regions as New Biomarkers in ST-Elevation Myocardial Infarction

Journal of cardiovascular development and disease, 2022-02, Vol.9 (2), p.58

2022

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May Argyrophilic Nucleolar Organizer Regions be the New Marker of a Hypoxic Response in Non ST Elevation Myocardial İnfarction?

Konuralp Tıp Dergisi, 2022-03, Vol.14 (1), p.132-141

2022

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May Argyrophilic Nucleolar Organizer Regions Be Used as a Biomarker for the Detection of the Degree of Ischemic Damage Instead of Tunel in Testicular Torsion?

Medicina (Kaunas, Lithuania), 2021-10, Vol.57 (11), p.1177

2021

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White–Sutton syndrome with hot water epilepsy and coexistence of SHOX gene variations

Acta neurologica Belgica, 2021-06, Vol.121 (3), p.749-755

2021

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Apoptosis-associated speck-like protein containing a CARD (ASC), TNF Like Factor 1a(TL-1a) and B Cell Chemoattractant Chemokine Ligand 13(CXCL-13) expression profiles in familial Mediterranean fever (FMF) patients

Konuralp Tıp Dergisi, 2023-03, Vol.15 (1), p.59-68

2023

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Clinical and molecular findings in a Turkish family with an ultra-rare condition, ELP2-related neurodevelopmental disorder

Molecular biology reports, 2021, Vol.48 (1), p.701-708

2021

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Investigation of the forkhead box protein P2 gene by the next-generation sequence analysis method in children diagnosed with specific learning disorder

Psychiatric genetics, 2023-02, Vol.33 (1), p.8-19

2023

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The role of macrophage in atherosclerosis: An overview

Erciyes Medical Journal, 2021-01

Damar, İbrahim Halil

2021

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Chorioretinal dystrophy, hypogonadotropic hypogonadism, and cerebellar ataxia: Boucher-Neuhauser syndrome due to a homozygous (c.3524C>G (p.Ser1175Cys)) variant in PNPLA6 gene

Ophthalmic genetics, 2021-06, Vol.42 (3), p.276-282

2021

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Evaluation of both expression and serum protein levels of caspase-8 and mitogen-activated protein kinase 1 genes in patients with different severities of COVID-19 infection

Molecular biology reports, 2023-04, Vol.50 (4), p.3241-3248

2023

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Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms (894G/T, −786T/C, G10T) and Clinical Findings in Patients with Migraine

Neuromolecular medicine, 2014-09, Vol.16 (3), p.587-593

2014

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Study of ten causal genes in Turkish patients with clinically suspected maturity-onset diabetes of the young (MODY) using a targeted next-generation sequencing panel

Molecular biology reports, 2022-08, Vol.49 (8), p.7483-7495

2022

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Bialelic Pathogenic (c.830G>A(p.R277Q)) Variant Disrupting the GNE Gene Function and Causes Nonaka myopathy Phenotype

Cytology and genetics, 2023-08, Vol.57 (4), p.347-355

2023

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Atypical presentation in patients with 17 α-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature

Turkish journal of pediatrics, 2020-09, Vol.62 (5), p.851-857

2020

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Congenital nephrotic syndrome secondary to pertussis

Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2020-03, Vol.40 (2), p.205-206

2020

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Evaluation of the Effects of Rapamycin Treatment on Antioxidant Enzyme Changes and AgNOR in Testicular Torsion

Konuralp Tıp Dergisi, 2021-03, Vol.13 (1), p.45-54

2021

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Clınıcal Approach To Patıents Wıth Klıppel-Feıl Syndrome

Konuralp Tıp Dergisi, 2021-03, Vol.13 (1), p.135-140

2021

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Evaluation of Cases with Myotonia Congenita for Cardiovascular Risk

Medeniyet medical journal, 2019, Vol.34 (4), p.374-379

2019

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Evaluation of Y Chromosome Microdeletion and Chromosome Analysis Results in Infertile Male Patients

Konuralp Tıp Dergisi, 2023-10, Vol.15 (3), p.383-389

2023

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Reduction of the argyrophilic nucleolar organizing region associated protein synthesis with age in buccal epithelial cells of healthy individuals

Aging clinical and experimental research, 2015-04, Vol.27 (2), p.201-208

2015

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Regiones organizadoras nucleolares argirófilas como un biomarcador esperanzador para la detección de niveles de hipoxia cerebral causados por diferentes dosis de intoxicación de monóxido de carbono

Gaceta médica de México, 2021-11, Vol.157 (6)

2021

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Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey

Breast (Edinburgh), 2022-10, Vol.65, p.15-22

2022

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Frequency of hereditary prothrombotic risk factors in patients with Down Syndrome

Konuralp Tıp Dergisi, 2021-03, Vol.13 (1), p.89-93

2021

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The Evaluation of the Genetic Variation Types of the Uridine Diphosphate Glucuronosyl Transferase 1A1 Gene by Next-Generation Sequencing and Their Effects on Bilirubin Levels in Obese Children

Does capsaicin have therapeutic benefits in human colon adenocarcinoma? Selection of the most reliable dose via AgNOR

Argyrophilic Nucleolar Organizer Regions as New Biomarkers in ST-Elevation Myocardial Infarction

May Argyrophilic Nucleolar Organizer Regions be the New Marker of a Hypoxic Response in Non ST Elevation Myocardial İnfarction?

May Argyrophilic Nucleolar Organizer Regions Be Used as a Biomarker for the Detection of the Degree of Ischemic Damage Instead of Tunel in Testicular Torsion?

White–Sutton syndrome with hot water epilepsy and coexistence of SHOX gene variations

Apoptosis-associated speck-like protein containing a CARD (ASC), TNF Like Factor 1a(TL-1a) and B Cell Chemoattractant Chemokine Ligand 13(CXCL-13) expression profiles in familial Mediterranean fever (FMF) patients

Clinical and molecular findings in a Turkish family with an ultra-rare condition, ELP2-related neurodevelopmental disorder

Investigation of the forkhead box protein P2 gene by the next-generation sequence analysis method in children diagnosed with specific learning disorder

The role of macrophage in atherosclerosis: An overview

Chorioretinal dystrophy, hypogonadotropic hypogonadism, and cerebellar ataxia: Boucher-Neuhauser syndrome due to a homozygous (c.3524C>G (p.Ser1175Cys)) variant in PNPLA6 gene

Evaluation of both expression and serum protein levels of caspase-8 and mitogen-activated protein kinase 1 genes in patients with different severities of COVID-19 infection

Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms (894G/T, −786T/C, G10T) and Clinical Findings in Patients with Migraine

Study of ten causal genes in Turkish patients with clinically suspected maturity-onset diabetes of the young (MODY) using a targeted next-generation sequencing panel

Bialelic Pathogenic (c.830G>A(p.R277Q)) Variant Disrupting the GNE Gene Function and Causes Nonaka myopathy Phenotype

Atypical presentation in patients with 17 α-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature

Congenital nephrotic syndrome secondary to pertussis

Evaluation of the Effects of Rapamycin Treatment on Antioxidant Enzyme Changes and AgNOR in Testicular Torsion

Clınıcal Approach To Patıents Wıth Klıppel-Feıl Syndrome

Evaluation of Cases with Myotonia Congenita for Cardiovascular Risk

Evaluation of Y Chromosome Microdeletion and Chromosome Analysis Results in Infertile Male Patients

Reduction of the argyrophilic nucleolar organizing region associated protein synthesis with age in buccal epithelial cells of healthy individuals

Regiones organizadoras nucleolares argirófilas como un biomarcador esperanzador para la detección de niveles de hipoxia cerebral causados por diferentes dosis de intoxicación de monóxido de carbono

Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey

Frequency of hereditary prothrombotic risk factors in patients with Down Syndrome

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