Citations

Showing 10 of 107906 citations.

Dual-Energy and Low-kVp CT in the Abdomen
Yeh, Benjamin M. , Wang, Zhen J. , Teh, Hui Seong , Hartman, Robert P. , Prevrhal, Sven, Shepherd, John

Mayo Clinic

American Journal of Roentgenology | June 19, 2009 | Volume: 193 | Issue: 1 | Pages: 47-54

10.2214/ajr.09.2592 | PMID 19542394 Get It

Keats & Kahn's Roentgen Atlas of Skeletal Maturation
Smith, Michael B.

Mayo Clinic

American Journal of Roentgenology | June 19, 2009 | Volume: 193 | Issue: 1 | Pages: W73-W73

10.2214/ajr.08.2267 Get It

Problem Solving in Musculoskeletal Imaging.
Garner, Hillary W.

Mayo Clinic

American Journal of Roentgenology | June 19, 2009 | Volume: 193 | Issue: 1 | Pages: W72-W72

10.2214/ajr.08.2244 Get It

Prospective Comparison of State-of-the-Art MR Enterography and CT Enterography in Small-Bowel Crohn's Disease
Siddiki, Hassan , Fidler, Jeff L. , Burton, Sharon S., Huprich, James E., Hough, David M., Johnson, C. Daniel, Bruining, David H. , Loftus, Edward V. , Sandborn, William J. , Pardi, Darrell S. , Mandrekar, Jayawant N. , Fidler, Jeff L. , Fletcher, Joel G. , Loftus, Edward V

Mayo Clinic

American Journal of Roentgenology | June 19, 2009 | Volume: 193 | Issue: 1 | Pages: 113-121

10.2214/ajr.08.2027 | PMID 19542402 Get It

Feasibility of In Vivo MR Elastographic Splenic Stiffness Measurements in the Assessment of Portal Hypertension
Talwalkar, Jayant A., Yin, Meng , Venkatesh, Sudhakar K. , Rossman, Phillip J. , Grimm, Roger C., Romano, Anthony J., Kamath, Patrick S. , Manduca, Armando , Ehman, Richard L. , Venkatesh, Sudhakar K , Yin, Meng

Mayo Clinic

American Journal of Roentgenology | June 19, 2009 | Volume: 193 | Issue: 1 | Pages: 122-127

10.2214/ajr.07.3504 | PMID 19542403 Get It

Advanced MRI Methods for Assessment of Chronic Liver Disease
Reeder, Scott B. , Taouli, Bachir , Ehman, Richard L. , Reeder, Scott B.

Mayo Clinic

American Journal of Roentgenology | June 19, 2009 | Volume: 193 | Issue: 1 | Pages: 14-27

10.2214/ajr.09.2601 | PMID 19542391 Get It

Is Diabetes Mellitus an Independent Risk Factor for Venous Thromboembolism?
Heit, John A. , Leibson, Cynthia L., Ashrani, Aneel A. , Petterson, Tanya M. , Bailey, Kent R. , Melton, L. Joseph

Mayo Clinic

Arteriosclerosis, Thrombosis, and Vascular Biology | June 19, 2009 | Volume: 29 | Issue: 9 | Pages: 1399-1405

10.1161/atvbaha.109.189290 | PMID 19542020 Get It

Objective— Although diabetes mellitus is reported as a risk factor for venous thromboembolism (VTE), persons with diabetes are frequently hospitalized for medical illness or surgery, or confined to a nursing home, all major VTE risk factors. Consequently, we tested diabetes for an independent association with incident VTE. Methods and Results— Using Rochester Epidemiology Project resources, we identified all Olmsted County, Minn residents who met objective criteria for incident VTE over the 25-year period, 1976 to 2000 (n=1922), and 1 to 2 resident controls per case, matched on age, gender, and length of medical history (n=2115). Complete medical histories in the community were reviewed for previously identified independent VTE risk factors and diabetes-related variables. We tested diabetes and diabetes complications (retinopathy, nephropathy or neuropathy, and ketoacidosis) as potential VTE risk factors, both alone and after adjusting for VTE risk factors. Univariately, diabetes by clinical diagnosis or by stricter criteria (fasting ambulatory blood glucose ≥140 mg/dL or antidiabetic drug therapy), and diabetes complications, were associated with overall incident VTE. However, after controlling for hospitalization for major surgery or medical illness and nursing home confinement, diabetes was no longer associated with VTE. Conclusion— Diabetes mellitus and diabetes complications are not independent risk factors for incident VTE.
Biodesign of a renal-protective peptide based on alternative splicing of B-type natriuretic peptide
Pan, Shuchong, Chen, Horng H. , Dickey, Deborah M., Boerrigter, Guido, Lee, Candace, Kleppe, Laurel S., Redfield, Margaret M. , Potter, Lincoln R. , Burnett, John C. , Simari, Robert D., Lee, Candace Y.W., Hall, Jennifer L. , Lerman, Amir

Mayo Clinic

Proceedings of the National Academy of Sciences | June 18, 2009 | Volume: 106 | Issue: 27 | Pages: 11282-11287

10.1073/pnas.0811851106 | PMID 19541613 Get It

Alternative RNA splicing may provide unique opportunities to identify drug targets and therapeutics. We identified an alternative spliced transcript for B-type natriuretic peptide (BNP) resulting from intronic retention. This transcript is present in failing human hearts and is reduced following mechanical unloading. The intron-retained transcript would generate a unique 34 amino acid (aa) carboxyl terminus while maintaining the remaining structure of native BNP. We generated antisera to this carboxyl terminus and identified immunoreactivity in failing human heart tissue. The alternatively spliced peptide (ASBNP) was synthesized and unlike BNP, failed to stimulate cGMP in vascular cells or vasorelax preconstricted arterial rings. This suggests that ASBNP may lack the dose-limiting effects of recombinant BNP. Given structural considerations, a carboxyl-terminal truncated form of ASBNP was generated (ASBNP.1) and was determined to retain the ability of BNP to stimulate cGMP in canine glomerular isolates and cultured human mesangial cells but lacked similar effects in vascular cells. In a canine-pacing model of heart failure, systemic infusion of ASBNP.1 did not alter mean arterial pressure but increased the glomerular filtration rate (GFR), suppressed plasma renin and angiotensin, while inducing natriuresis and diuresis. Consistent with its distinct in vivo effects, the activity of ASBNP.1 may not be explained through binding and activation of NPR-A or NPR-B. Thus, the biodesigner peptide ASBNP.1 enhances GFR associated with heart failure while lacking the vasoactive properties of BNP. These findings demonstrate that peptides with unique properties may be designed based on products of alternatively splicing.
Pleural Effusions: Etiology, Diagnosis, and Management
Cordes, Mary Ellen

Mayo Clinic

The Journal of Continuing Education in Nursing | June 18, 2009 | Volume: 40 | Issue: 6 | Pages: 248-249

10.3928/00220124-20090522-03 | PMID 19639912 Get It

This column describes the etiology, diagnosis, and management of pleural effusions. J Contin Educ Nurs 2009;40(6):248–249.
Automated Cellular Imaging System III for Assessing HER2 Status in Breast Cancer Specimens
Minot, Douglas M., Kipp, Benjamin R. , Root, Renee M., Meyer, Reid G., Reynolds, Carol, Nassar, Aziza , Henry, Michael , Clayton, Amy C., Root, Renee R., Nassar, Aziza

Mayo Clinic

American Journal of Clinical Pathology | June 18, 2009 | Volume: 132 | Issue: 1 | Pages: 133-138

10.1309/ajcpjv0skaf2pcmy | PMID 19864244 Get It

Abstract The goal of this study was to assess the performance characteristics of the Automated Cellular Imaging System (ACIS III) for HER2 immunohistochemical analysis. The study was performed on 187 biopsy slides from patients who underwent HER2 testing between January and February 2008. Three scoring methods by the ACIS III were compared with the manual score and fluorescence in situ hybridization (FISH) results for HER2 amplification. The equal distribution score (EQD) method, in which 2 areas each of high-, moderate-, and low-intensity staining were measured, most closely matched the FISH HER2 amplification result. The numbers of immunohistochemically negative (0 or 1+)/FISH+ cases were equivalent for all methods. The EQD method had significantly fewer 2+ cases (n = 16) (P < .001) vs the manual method (n = 35) and yielded a higher positive predictive value (38%) for HER2 amplification compared with the manual method (20%). The EQD method may more accurately identify FISH-amplified HER2 cases with fewer 2+ cases that would be “reflexed” to FISH compared with the manual method.