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Toplam kayıt 36, listelenen: 31-36
Advantages and pitfalls of the glycated hemoglobin A1c measurement in acute coronary syndrome: Start simple, evolve to more sophisticated
(SAGE Publications Inc., 2019)
We would like to thank Cetin et al1 for their interest in our work titled, “Association of Prediabetes With Higher Coronary Atherosclerotic Burden Among Patients With First Diagnosed Acute Coronary Syndrome”2 about the ...
From the obesity tsunami to the diabetes avalanche: Primordial prevention of the diabesity-related cardiovascular epidemic by diabeto-cardiologists
(SAGE Publications Inc., 2019)
We thank Demirtas et al1 for their interest in our paper entitled “Association of Prediabetes With Higher Coronary Atherosclerotic Burden Among Patients With First Diagnosed Acute Coronary Syndrome”2 about the association ...
A Novel Permutation Based Solution Representation Technique for Vehicle Routing Problems on GPUs
(2021)
In this study, the vehicle routing problem (VRP) which is a well-known NP-hard combinatorial optimization problem is handled on graphic processing units (GPUs). Solving any kind of VRP is extremely hard when the instance ...
In Silico Analysis of miRNA-mediated ceRNAs as Potential Molecular Biomarkers in Glioblastoma
(2021)
Objectives: Glioblastoma multiforme (GBM) is defined as the most frequent and lethal form of the primary brain tumors in the central nervous system (CNS) in adults. Recent studies have focused on the identification of the ...
The Importance of Imaging and Fine Needle Aspiration Biopsy in Primary Benign Parapharyngeal Space Tumors
(2021)
Objective: The purpose of this study is the comparison of the radiological pre-diagnosis with the cytopathological results acquired from fine needle aspiration biopsy (FNAB) and the post-operative final histopathological ...
Case of cerebrotendinous xanthomatosis with giant xanthomas and literature review
(SPRINGER, 2023)
Introduction Cerebrotendinous xanthomatosis (CTX) is a rare autosomalrecessive disease that occurs as result of mutation in the CYP27A1 gene. Theclinical presentation of the disease is quite wide. We planned to briefyreview ...