Institution
University of Texas Health Science Center at Houston
Education•Houston, Texas, United States•
About: University of Texas Health Science Center at Houston is a education organization based out in Houston, Texas, United States. It is known for research contribution in the topics: Population & Cancer. The organization has 27309 authors who have published 42520 publications receiving 2151596 citations. The organization is also known as: UTHealth & The UT Health Science Center at Houston.
Topics: Population, Cancer, Poison control, Medicine, Health care
Papers published on a yearly basis
Papers
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TL;DR: These insights point the way for further research to establish definitive causes of specific types of cell injury and cell death, and they provide important clues for the design of improved diagnostic approaches and therapeutic interventions.
Abstract: Apoptosis and necrosis are two fundamental types of cell death. Current knowledge indicates that the key mechanism of apoptosis is endonuclease activation leading to internucleosomal double-stranded chromatin (DNA) breaks, whereas the key mechanism of necrosis is cell membrane damage. The initial alterations of cellular metabolism and electrolyte homeostasis induced by an injurious agent may activate at least four major pathways leading to loss of membrane integrity: membrane phospholipid degradation, production of amphipathic lipids, damage to the cytoskeleton, and generation of toxic oxygen species and free radicals. These insights point the way for further research to establish definitive causes of specific types of cell injury and cell death, and they provide important clues for the design of improved diagnostic approaches and therapeutic interventions.
360 citations
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TL;DR: Endothelium produces and secretes von Willebrand factor, which mediates platelet adhesion and shear-stress-induced aggregation, and releases prostacyclin and nitric oxide, potent inhibitors of platelet and monocyte activation and vasodilators.
Abstract: Vascular endothelium is strategically located at the interface between tissue and blood. It is pivotal for protecting against vascular injury and maintaining blood fluidity. Normal endothelium releases prostacyclin and nitric oxide, potent inhibitors of platelet and monocyte activation and vasodilators. Their syntheses are governed by isoforms of enzymes. Normal endothelial surface expresses ecto-adenosine diphosphatase, which degrades adenosine diphosphate and inhibits platelet aggregation; thrombomodulin, which serves as a binding site for thrombin to activate protein C; and heparin-like molecules, which serve as a cofactor for antithrombin III. Normal endothelium secretes tissue plasminogen activator, which activates the fibrinolysis system. Endothelium produces and secretes von Willebrand factor, which mediates platelet adhesion and shear-stress-induced aggregation. Injury to endothelium is accompanied by loss of protective molecules and expression of adhesive molecules, procoagulant activities, and mitogenic factors, leading to development of thrombosis, smooth muscle cell migration, and proliferation and atherosclerosis.
360 citations
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TL;DR: It is suggested that transthoracic vertebrectomy and spinal stabilization can improve the quality of life considerably in cancer patients with spinal metastasis by restoring or preserving ambulation and by controlling intractable spinal pain with acceptable rates of morbidity and mortality.
Abstract: Object. Anterior approaches to the spine for the treatment of spinal tumors have gained acceptance; however, in most published reports, patients with primary, metastatic, or chest wall tumors involving cervical, thoracic, or lumbar regions of the spine are combined. The purpose of this study was to provide a clear perspective of results that can be expected in patients who undergo anterior vertebral body resection, reconstruction, and stabilization for spinal metastases that are limited to the thoracic region. Methods. Outcome is presented for 72 patients with metastatic spinal tumors who were treated by transthoracic vertebrectomy at The University of Texas M. D. Anderson Cancer Center. The predominant primary tumors included renal cancer in 19 patients, breast cancer in 10, melanoma or sarcoma in 10, and lung cancer in nine patients. The most common presenting symptoms were back pain, which occurred in 90% of patients, and lower-extremity weakness, which occurred in 64% of patients. All patients underwe...
360 citations
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Roswell Park Cancer Institute1, Santa Clara Valley Medical Center2, Stanford University3, University of Texas Health Science Center at Houston4, Wayne State University5, University of Genoa6, National Institutes of Health7, Katholieke Universiteit Leuven8, University of Texas Health Science Center at San Antonio9, Duke University10, University of Paris11, University of Florida12, University of Lausanne13, University of Michigan14, Harvard University15, University of Alabama16, University of Texas MD Anderson Cancer Center17, University of Milan18, Medical University of Vienna19, University of Manitoba20, Radboud University Nijmegen21
TL;DR: An expert international panel consisting of the Mycoses Study Group and the European Organization for Research and Treatment of Cancer was convened to propose guidelines for assessing treatment responses in clinical trials of IFDs and for defining study outcomes.
Abstract: Invasive fungal diseases (IFDs) have become major causes of morbidity and mortality among highly immunocompromised patients. Authoritative consensus criteria to diagnose IFD have been useful in establishing eligibility criteria for antifungal trials. There is an important need for generation of consensus definitions of outcomes of IFD that will form a standard for evaluating treatment success and failure in clinical trials. Therefore, an expert international panel consisting of the Mycoses Study Group and the European Organization for Research and Treatment of Cancer was convened to propose guidelines for assessing treatment responses in clinical trials of IFDs and for defining study outcomes. Major fungal diseases that are discussed include invasive disease due to Candida species, Aspergillus species and other molds, Cryptococcus neoformans, Histoplasma capsulatum, and Coccidioides immitis. We also discuss potential pitfalls in assessing outcome, such as conflicting clinical, radiological, and/or mycological data and gaps in knowledge.
360 citations
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Henry Ford Health System1, Icahn School of Medicine at Mount Sinai2, Medical University of South Carolina3, University of Texas Health Science Center at Houston4, Emory University5, University of Virginia6, Mayo Clinic7, University of Cincinnati8, University of Missouri9, University of California, San Diego10, National Institutes of Health11, University of Kansas12
TL;DR: The analysis suggests that EICs are prevalent within 3 hours of stroke onset and correlate with stroke severity, however, Eics are not independently associated with increased risk of adverse outcome after rt-PA treatment.
Abstract: ContextThe prevalence and clinical significance of early ischemic changes (EICs)
on baseline computed tomography (CT) scan of the head obtained within 3 hours
of ischemic stroke are not established.ObjectiveTo determine the frequency and significance of EIC on baseline head
CT scans in the National Institute of Neurological Disorders and Stroke (NINDS)
rt-PA (recombinant tissue plasminogen activator) Stroke Trial.Design and SettingThe original study, a randomized controlled trial, took place from January
1991 through October 1994 at 43 sites, during which CT images were obtained
within 3 hours of symptom onset and prior to the initiation of rt-PA or placebo.
For the current analysis, detailed reevaluation was undertaken after October
1994 of all baseline head CT scans with clinical data available pretreatment
(blinded to treatment arm).PatientsOf 624 patients enrolled in the trial, baseline CT scans were retrieved
and reviewed for 616 (99%).Main Outcome MeasuresFrequency of EICs on baseline CT scans; association of EIC with other
baseline variables; effect of EICs on deterioration at 24 hours (≥4 points
increase from the baseline National Institutes of Health Stroke Scale [NIHSS]
score); clinical outcome (measured by 4 clinical scales) at 3 months, CT lesion
volume at 3 months, death at 90 days; and symptomatic intracranial hemorrhage
(ICH) within 36 hours of treatment.ResultsThe prevalence of EIC on baseline CT in the combined rt-PA and placebo
groups was 31% (n = 194). The EIC was significantly associated with baseline
NIHSS score (ρ = 0.23; P<.001) and time from
stroke onset to baseline CT scan (ρ = 0.11; P
= .007). After adjusting for baseline variables, there was no EIC ×
treatment interaction detected for any clinical outcome, including deterioration
at 24 hours, 4 clinical scales, lesion volume, and death at 90 days (P≥.25), implying that EIC is unlikely to affect response
to rt-PA treatment. After adjusting for NIHSS score (an independent predictor
of ICH), no EIC association with symptomatic ICH at 36 hours was detected
in the group treated with rt-PA (P≥.22).ConclusionsOur analysis suggests that EICs are prevalent within 3 hours of stroke
onset and correlate with stroke severity. However, EICs are not independently
associated with increased risk of adverse outcome after rt-PA treatment. Patients
treated with rt-PA did better whether or not they had EICs, suggesting that
EICs on CT scan are not critical to the decision to treat otherwise eligible
patients with rt-PA within 3 hours of stroke onset.
360 citations
Authors
Showing all 27450 results
Name | H-index | Papers | Citations |
---|---|---|---|
Paul M. Ridker | 233 | 1242 | 245097 |
Eugene Braunwald | 230 | 1711 | 264576 |
Eric N. Olson | 206 | 814 | 144586 |
Hagop M. Kantarjian | 204 | 3708 | 210208 |
André G. Uitterlinden | 199 | 1229 | 156747 |
Gordon B. Mills | 187 | 1273 | 186451 |
Eric Boerwinkle | 183 | 1321 | 170971 |
Bruce M. Psaty | 181 | 1205 | 138244 |
Aaron R. Folsom | 181 | 1118 | 134044 |
Daniel R. Weinberger | 177 | 879 | 128450 |
Bharat B. Aggarwal | 175 | 706 | 116213 |
Richard A. Gibbs | 172 | 889 | 249708 |
Russel J. Reiter | 169 | 1646 | 121010 |
James F. Sallis | 169 | 825 | 144836 |
Steven N. Blair | 165 | 879 | 132929 |