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Social Studies Teacher Candidates’ Perceptions of Historical Concepts

Cukurova University Faculty of Education Journal, 2024-04, Vol.53 (1), p.206-242

2024

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Bacterial and fungal communities in chronic rhinosinusitis with nasal polyps

PloS one, 2024-05, Vol.19 (5), p.e0304634

2024

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A Disseminated Echinococcosis Patient with Five Years Survival from Turkey: A Case Report

Iranian journal of parasitology, 2023, Vol.18 (2), p.262-267

2023

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Meier-Gorlin syndrome type 7: a rare cause of primordial dwarfism: two new cases and literature review

Clinical dysmorphology, 2024-10, Vol.33 (4), p.167-170

2024

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Autosomal recessive otospondylo-mega-epiphyseal dysplasia: comprehensive clinical review of a pediatric cohort

Clinical dysmorphology, 2023-10, Vol.32 (4), p.151-155

2023

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Preparation of electrospun polyurethane nanofiber mats for the release of doxorubicine

Journal of materials science. Materials in medicine, 2018-01, Vol.29 (1), p.8-9, Article 8

2018

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Surveillance of hemodialysis related infections: a prospective multicenter study

Scientific reports, 2022-12, Vol.12 (1), p.22240-22240, Article 22240

2022

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Risk factors for linezolid-associated thrombocytopenia and negative effect of carbapenem combination

Journal of infection in developing countries, 2019-10, Vol.13 (10), p.886-891

2019

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A Pulmonary Tuberculosis Case Presented with Tonsillar Involvement

Turkish Thoracic Journal, 2016-07, Vol.17 (3), p.122-124

2016

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Evaluation of Risk Factors for Antibiotic Resistance in Patients with Nosocomial Infections Caused by Pseudomonas aeruginosa

The Canadian journal of infectious diseases & medical microbiology, 2016-01, Vol.2016 (2016), p.1-9

2016

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Two Different Diseases with Uric Acid Abnormality in the Same Patient: Be Careful About Routine Biochemical Tests

Klinische Pädiatrie, 2023-09, Vol.235 (5), p.308-309

2023

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A Rare Treatable Cause of Cardiomyopathy: Primary Carnitine Deficiency

Molecular syndromology, 2024-03, Vol.15 (2), p.156-160

2024

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Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy

Molecular syndromology, 2024-09, p.1-14

2024

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Efficacy of flecainide in bidirectional ventricular tachycardia and tachycardia-induced cardiomyopathy with Andersen-Tawil syndrome

European journal of medical genetics, 2022-06, Vol.65 (6), p.104499-104499, Article 104499

2022

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New cases of recently described Thauvin‐Robinet‐Faivre syndrome with a novel homozygous FIBP gene variant

American journal of medical genetics. Part A, 2024-03, Vol.194 (3), p.e63449-n/a

2024

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Triple X Syndrome with a Rare Finding: Cleft Palate

The journal of pediatric research, 2018-06, Vol.5 (2), p.100-102

2018

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Investigation of Microbial Etiology in Endotracheal Aspirate Samples of Severe Pneumonia Patients by Multiplex PCR and Culture Method

KLIMIK dergisi, 2022-09, Vol.35 (3), p.179-185

2022

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Neuroprotective potential of the fruit (acorn) from Quercus coccifera L

Turkish journal of agriculture and forestry, 2018-01, Vol.42 (2)

2018

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A review of research on social studies instruction for students with intellectual disabilities

Journal of intellectual disabilities, 2024-06, p.17446295241259074

2024

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Novel mutations in GALNT3 causing hyperphosphatemic familial tumoral calcinosis

Journal of bone and mineral metabolism, 2011-09, Vol.29 (5), p.621-625

2011

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Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa

American journal of human genetics, 2016-07, Vol.99 (1), p.236-245

2016

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Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa

American journal of human genetics, 2018-04, Vol.102 (4), p.713-713

2018

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A patient with mitochondrial disorder due to a novel mutation in MRPS22

Metabolic brain disease, 2017-10, Vol.32 (5), p.1389-1393

2017

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The Role of Brand Image in Buying Attitude of the Consumers: Northern Part of Cyprus Model

Revista de cercetare şi intervenţie socialǎ, 2016-06, Vol.53, p.132

2016

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A Case of Nosocomial Prosthetic Valve Endocarditis Due to Pseudomonas aeruginosa Associated With Complications

KLIMIK dergisi, 2020-05, Vol.33 (1), p.91-94

2020

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Social Studies Teacher Candidates’ Perceptions of Historical Concepts

Bacterial and fungal communities in chronic rhinosinusitis with nasal polyps

A Disseminated Echinococcosis Patient with Five Years Survival from Turkey: A Case Report

Meier-Gorlin syndrome type 7: a rare cause of primordial dwarfism: two new cases and literature review

Autosomal recessive otospondylo-mega-epiphyseal dysplasia: comprehensive clinical review of a pediatric cohort

Preparation of electrospun polyurethane nanofiber mats for the release of doxorubicine

Surveillance of hemodialysis related infections: a prospective multicenter study

Risk factors for linezolid-associated thrombocytopenia and negative effect of carbapenem combination

A Pulmonary Tuberculosis Case Presented with Tonsillar Involvement

Evaluation of Risk Factors for Antibiotic Resistance in Patients with Nosocomial Infections Caused by Pseudomonas aeruginosa

Two Different Diseases with Uric Acid Abnormality in the Same Patient: Be Careful About Routine Biochemical Tests

A Rare Treatable Cause of Cardiomyopathy: Primary Carnitine Deficiency

Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy

Efficacy of flecainide in bidirectional ventricular tachycardia and tachycardia-induced cardiomyopathy with Andersen-Tawil syndrome

New cases of recently described Thauvin‐Robinet‐Faivre syndrome with a novel homozygous FIBP gene variant

Triple X Syndrome with a Rare Finding: Cleft Palate

Investigation of Microbial Etiology in Endotracheal Aspirate Samples of Severe Pneumonia Patients by Multiplex PCR and Culture Method

Neuroprotective potential of the fruit (acorn) from Quercus coccifera L

A review of research on social studies instruction for students with intellectual disabilities

Novel mutations in GALNT3 causing hyperphosphatemic familial tumoral calcinosis

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa

A patient with mitochondrial disorder due to a novel mutation in MRPS22

The Role of Brand Image in Buying Attitude of the Consumers: Northern Part of Cyprus Model

A Case of Nosocomial Prosthetic Valve Endocarditis Due to Pseudomonas aeruginosa Associated With Complications

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