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5955 citation(s) found for "Wu, Joseph".

Real-Time PCR in Clinical Microbiology: Applications for Routine Laboratory Testing
Espy, Mark J., Uhl, J. R., Sloan, Lynne M., Buckwalter, Seanne P., Jones, Mary F. , Vetter, Emily A., Yao, Joseph D. , Wengenack, Nancy L. , Rosenblatt, Jon E., Cockerill, F. R., Smith, T. F., Cockerill, Franklin R.

Clinical Microbiology Reviews | July 17, 2006 | Volume: 19 | Issue: 3 | Pages: 595-595

10.1128/cmr.00022-06 Get It

Bringing Molecular Biology to Bear on Adhesion Prevention: Postsurgical Adhesion Reduction Using Intraperitoneal Inoculation of Hyaluronic Acid–Inducing Adenoviral Vector in a Murine Model
Hammer, Robert A., Morse, Abraham N. , Cornella, Jeffrey L. , Keller, Rebecca S., Hentz, Joseph G. , McDonald, John A., Loftus, Joseph C.

Journal of Gynecologic Surgery | July 13, 2006 | Volume: 22 | Issue: 1 | Pages: 7-18

10.1089/gyn.2006.22.7 Get It

Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MND
Josephs, Keith A. , Whitwell, Jennifer L. , Parisi, Joseph E., Petersen, Ronald C. , Dickson, Dennis W. , Knopman, David S. , Boeve, Bradley F. , Dickson, Dennis W

Neurology | July 12, 2006 | Volume: 65 | Issue: 4 | Pages: 645-647

10.1212/01.wnl.0000173178.67986.7f | PMID 16116138 Get It

Abnormal co-contraction in yips-affected but not unaffected golfers: Evidence for focal dystonia
Crews, Debra J., Hentz, Joseph G. , Smith, Aynsley M., Caviness, John N., Adler, Charles H.

Neurology | July 12, 2006 | Volume: 64 | Issue: 10 | Pages: 1813-1814

10.1212/01.wnl.0000162024.05514.03 | PMID 15911823 Get It

Healing of Canine Tendon in Zones Subjected to Different Mechanical Forces
Nessler, Joseph P., Amadio, Peter C. , Berglund, L. J., An, Kai‐Nan

Journal of Hand Surgery | July 6, 2006 | Volume: 17 | Issue: 5 | Pages: 561-568

10.1016/s0266-7681(05)80242-6 | PMID 1479251 Get It

The effect of external force environment on the healing of a partial thickness injury to canine flexor tendon was studied. A 50% laceration was made in either the fibrocartilaginous (compressive) zone or in the tendinous (tensile) zone of canine flexor digitorum profundus tendons. After three or six weeks, the tendons were harvested. An optical method for determining zone-specific material properties showed that, in response to injury, the structural stiffness decreased in the tensile zone of the tendon but increased in the compressive zone. The mechanical properties and failure mechanism of canine tendon and their changes in response to injury vary according to tendon zone, and differences in the healing process in mechanically specialised zones of the flexor tendon are discussed.
A phase I study of chlorozotocin (NSC 178248)
Kovach, John S., Moertel, Charles G., Schutt, Allen J., Frytak, Stephen, Rubin, Joseph, O’Connell, Michael J. , Ingle, James N.

Cancer | June 26, 2006 | Volume: 43 | Issue: 6 | Pages: 2189-2196

10.1002/1097-0142(197906)43:6<2189::aid-cncr2820430605>3.0.co;2-# | PMID 156580 Get It

Lack of Evidence for an Association Between Hemodynamic Variables and Hematoma Growth in Spontaneous Intracerebral Hemorrhage
Jauch, Edward C. , Lindsell, Christopher J. , Barsan, William G. , Pancioli, Arthur , Brott, Thomas G. , Adeoye, Opeolu M , Khoury, Jane , Broderick, Joseph P.

Stroke | June 23, 2006 | Volume: 37 | Issue: 8 | Pages: 2061-2065

10.1161/01.str.0000229878.93759.a2 | PMID 16794216 Get It

Background and Purpose— Early hematoma expansion in spontaneous intracerebral hemorrhage (ICH) is associated with worse clinical outcome. We hypothesized that hemodynamic parameters are associated with the increase in hematoma volume owing to their relationship to blood vessel wall stresses. Methods— We performed a post hoc analysis of clinical and computed tomography (CT) data from patients enrolled in a prospective observational study of ICH patients presenting within 3 hours from symptom onset. Hematoma volumes were measured at hospital arrival and at 1 and 20 hours from presentation. Blood pressure and heart rate, recorded at 19 time points between presentation and 20 hours, were used to derive hemodynamic variables. Multivariable logistic-regression models were constructed to assess the relation between hemodynamic parameters and hematoma growth, adjusted for clinical covariates. Results— From the original study, 98 patients underwent baseline and 1-hour CT scans; of these, 65 had 20-hour CT scans. Substantial hematoma growth was observed in 28% within the first hour. Of the 65 patients not undergoing surgery within 20 hours, 37% experienced hematoma growth by 20 hours. Neither baseline or peak hemodynamic parameters nor changes in hemodynamic parameters were significantly associated with hematoma growth at either 1 or 20 hours. Conclusions— We found no blood pressure or heart rate parameters, individually or in combination, that were associated with hematoma growth. Our data suggest the influence of hemodynamic parameters on vessel wall stress to be an unlikely target for intervention in reducing the risk of early hematoma growth in ICH.
Schistosoma mansoni infection in eosinophil lineage–ablated mice
Swartz, Jonathan M. , Dyer, Kimberly D., Cheever, Allen W., Ramalingam, Thirumalai R. , Pesnicak, Lesley, Domachowske, Joseph B. , Lee, James J. , Lee, Nancy A., Foster, Paul S. , Wynn, Thomas A. , Rosenberg, Helene F.

Blood | June 14, 2006 | Volume: 108 | Issue: 7 | Pages: 2420-2427

10.1182/blood-2006-04-015933 | PMID 16772607 Get It

AbstractWe explore the controversial issue of the role of eosinophils in host defense against helminthic parasites using the established Schistosoma mansoni infection model in 2 novel mouse models of eosinophil lineage ablation (ΔdblGATA and TgPHIL). No eosinophils were detected in bone marrow of infected ΔdblGATA or TgPHIL mice, despite the fact that serum IL-5 levels in these infected mice exceeded those in infected wild type by approximately 4-fold. Liver granulomata from infected ΔdblGATA and TgPHIL mice were likewise depleted of eosinophils compared with those from their respective wild types. No eosinophil-dependent differences in granuloma number, size, or fibrosis were detected at weeks 8 or 12 of infection, and differential accumulation of mast cells was observed among the ΔdblGATA mice only at week 12. Likewise, serum levels of liver transaminases, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) increased in all mice in response to S mansoni infection, with no eosinophil-dependent differences in hepatocellular damage observed. Finally, eosinophil ablation had no effect on worm burden or on egg deposition. Overall, our data indicate that eosinophil ablation has no impact on traditional measures of disease in the S mansoni infection model in mice. However, eosinophils may have unexplored immunomodulatory contributions to this disease process.
Improving Hyperglycemia Management in the Intensive Care Unit
Osburne, Robert C., Stockton, Lawrence, Baird, Marianne , Harmon, Valerie L., Keddo, Annie, Pounds, Teresa, Lowey, Linda, Reid, Joyce, McGowan, Kathryn A., Davidson, Paul C., Cook, Curtiss B.

The Diabetes Educator | June 13, 2006 | Volume: 32 | Issue: 3 | Pages: 394-403

10.1177/0145721706288072 | PMID 16772655 Get It

Purpose The purpose of this study was to assess the feasibility of a nurse-driven effort to improve hyperglycemia management in the intensive care unit (ICU) setting. Methods The setting was the ICU of a large urban hospital. The program was composed of 3 components: nurses as leaders, a clinical pathway to identify patients in need of hyperglycemia therapy, and implementation of a redesigned insulin infusion algorithm (the Columnar Insulin Dosing Chart). Time to reach a target glucose range of 80 to 110 mg/dL (4.4-6.1 mmol/L) was evaluated. Results One hundred sixteen ICU nurses were trained in the project. The Columnar Insulin Dosing Chart was applied to 20 patients. The average time required to reach the target blood glucose range was 12.8 hours. Below-target blood glucose levels were 6.9% of all blood glucose levels recorded, but only 0.9% were below 60 mg/dL (3.3 mmol/L). There was no sustained hypoglycemia, and no persistent clinical findings attributable to hypoglycemia were noted. Barriers to implementing the project included an increased nursing workload, the need for more finger-stick blood glucose monitors, and the need to acquire new finger-lancing devices that allowed for shallower skin puncture and increased patient comfort. Conclusions Tighter glycemic control goals can be attained in a busy ICU by a nurse-led team using a pathway for identifying and treating hyperglycemia, clear decision support tools, and adequate nurse education. The novel chart based insulin infusion algorithm chosen as the standard for this pilot was an effective tool for reducing the blood glucose to target range with no clinically significant hypoglycemia.
Immunoglobulin free light chains and solitary plasmacytoma of bone
Dingli, David , Kyle, Robert A. , Rajkumar, S. Vincent , Nowakowski, Grzegorz S. , Bida, John P., Therneau, Terry M. , Melton, L. Joseph, Dispenzieri, Angela , Katzmann, Jerry A., Larson, Dirk R. , Gertz, Morie A. , Rajkumar, S Vincent , Dispenzieri, Angela , Dingli, David

Blood | June 1, 2006 | Volume: 108 | Issue: 6 | Pages: 1979-1983

10.1182/blood-2006-04-015784 | PMID 16741249 Get It

Abstract An abnormal serum immunoglobulin free light chain (FLC) ratio at diagnosis may identify risk of progression to myeloma in patients with solitary bone plasmacytoma (SBP). In the cohort of 116 patients, 43 have progressed to myeloma, with a median time to progression of 1.8 years. The FLC ratio was determined in all 116 patients on serum collected at time of diagnosis and was abnormal in 54 patients (47%). An abnormal FLC ratio was associated with a higher risk of progression to myeloma (P = .039). The risk of progression at 5 years was 44% in patients with an abnormal serum FLC ratio at diagnosis compared with 26% in those with a normal FLC ratio. One to 2 years following diagnosis, a persistent serum M protein level of 5 g/L (0.5 g/dL) or higher was an additional risk factor for progression. A risk stratification model was constructed using the 2 variables of FLC ratio and M protein level: patients with a normal FLC ratio at baseline and M protein level less than 5 g/L (0.5 g/dL) at 1 to 2 years following diagnosis (low risk, n = 31); with either risk factor abnormal (intermediate risk, n = 26); and with both an abnormal FLC ratio and M protein level of 5 g/L (0.5 g/dL) or higher (high risk, n = 18). The corresponding progression rates at 5 years were significantly different in the low, intermediate, and high groups: 13%, 26%, and 62%, respectively (P < .001).