automated matlab 2017 program (MathWorks Inc)
Structured Review
Automated Matlab 2017 Program, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/automated+matlab+program/pm40261661-44-3-6
Average 90 stars, based on 1 article reviews
Images
Related Articles
other:Article Title: Quantitative Evaluation of Retinal Microvascular Abnormalities in Patients With Type 2 Diabetes Mellitus Without Clinical Sign of Diabetic Retinopathy Article Snippet: In this study, we quantified the retinal microvasculature from both macular and optic disc OCTA scans using an automated Article Title: Vagus nerve stimulation rate and duration determine whether sensory pairing produces neural plasticity Article Snippet: Data analysis All groups were analyzed using an automated Article Title: Vagus nerve stimulation rate and duration determine whether sensory pairing produces neural plasticity Article Snippet: All groups were analyzed using an automated Article Title: Real-Time 2D MR Cine From Beam Eye’s View With Tumor-Volume Projection to Ensure Beam-to-Tumor Conformality for MR-Guided Radiotherapy of Lung Cancer Article Snippet: Mimicking a 6-beam IMRT plan, all TR-4DMRI images in the patient-specific libraries were segmented for tumor volume using an automated Article Title: Role of intra-tumoral vasculature imaging features on susceptibility weighted imaging in differentiating primary central nervous system lymphoma from glioblastoma: a multiparametric comparison with pathological validation. Article Snippet: Purpose Primary objective of this study was to retrospectively evaluate the potential of a range of qualitative and quantitative multiparametric features assessed on T2, post-contrast T1, DWI, DCE-MRI, and susceptibility-weighted-imaging (SWI) in differentiating evenly sampled cohort of primary-central-nervous-system-lymphoma (PCNSL) vs glioblastoma (GB) with pathological validation.. Methods The study included MRI-data of histopathologically confirmed ninety-five GB and PCNSL patients scanned at 3.0 T MRI.. A total of six qualitative features (three from T2 and post-contrast T1, three from SWI: thin-linear-uninterrupted-intra-tumoral-vasculature, broken-intra-tumoral-microvasculature, hemorrhage) were analyzed by three independent radiologists. Article Title: Peripapillary Choroid Thickness as a Predisposing Factor for Nonarteritic Anterior Ischemic Optic Neuropathy: A Semiautomated OCT Study Article Snippet: However, we sought to eliminate measurement errors by using an automated Article Title: Comparison of Peripapillary Vessel Density of Acute Nonarteritic Anterior Ischemic Optic Neuropathy and Other Optic Neuropathies With Disc Swelling Using Optical Coherence Tomography Angiography: A Pilot Study Article Snippet: Background: The purpose of this study is to quantitatively compare the peripapillary vessel density (PPVD), measured with optical coherence tomography angiography (OCT-A), between acute nonarteritic anterior ischemic optic neuropathy (NAION) and other causes of disc swelling (“others”).. Methods: In this prospective comparative case series, patients with unilateral disc swelling due to acute NAION (n = 7) and “others” (n = 7) underwent OCT-A scanning of the optic nerve head with a swept-source OCT (Triton DRIOCT), in addition to functional assessment.. OCT-A images were analyzed using an automated customized MATLAB program. Staining:Article Title: Evaluating the Accuracy of FUCCI Cell Cycle In Vivo Fluorescent Imaging to Assess Tumor Proliferation in Preclinical Oncology Models. Article Snippet: Purpose The primary goal of this study is to evaluate the accuracy of the fluorescence ubiquitination cell cycle indicator (FUCCI) system with fluorescence in vivo imaging compared to 3′-deoxy-3′-[18F]fluorothymidine ([18F]-FLT) positron emission tomography (PET)/computed tomography (CT) and biological validation through histology.. Imaging with [18F]-FLT PET/CT can be used to noninvasively assess cancer cell proliferation and has been utilized in both preclinical and clinical studies.. However, a cost-effective and straightforward method for in vivo, cell cycle targeted cancer drug screening is needed prior to moving towards translational imaging methods such as PET/CT. |
