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1134 citation(s) found for "Ma, Julia".

P1‐252: Evaluation of Cognitive Endophenotypes for Association with CLU, CR1 and PICALM LOAD Risk Genes
Pedraza, Otto , Allen, Mariet , Jennette, Kyle J. , Carrasquillo, Minerva M. , Palusak, Ryan, Nguyen, Thuy , Malphrus, Kimberly G., Ivnik, Robert J., Pankratz, Shane, Graff‐Radford, Neill, Roberts, Rosebud O., Petersen, Ronald C. , Younkin, Steven G., Ertekin‐Taner, Nilüfer , Crook, Julia E. , Carrasquillo, Minerva M. , Smith, Glenn E. , Knopman, David S. , Graff‐Radford, Neill

Alzheimer's & Dementia | August 1, 2011 | Volume: 7 | Issue: 4S_Part_6 | Pages: No page available

10.1016/j.jalz.2011.05.532 Get It

P1‐458: Differential association of memory endophenotypes to APOE alleles
Pedraza, Otto , Allen, Mariet , Ivnik, Robert J., Graff‐Radford, Neill R. , Roberts, Rosebud O., Petersen, Ronald C. , Younkin, Steven G., Ertekin‐Taner, Nilüfer , Crook, Julia E. , Smith, Glenn E. , Knopman, David S. , Pankratz, V. Shane

Alzheimer's & Dementia | August 1, 2011 | Volume: 7 | Issue: 4S_Part_7 | Pages: No page available

10.1016/j.jalz.2011.05.740 Get It

Cardiovagal Autonomic Function in HIV-Infected Patients with Unsuppressed HIV Viremia
Chow, Dominic C. , Wood, Robert , Choi, Julia, Grandinetti, Andrew, Gerschenson, Mariana , Sriratanaviriyakul, Narin, Nakamoto, Beau K. , Shikuma, Cecilia M. , Low, Phillip A.

HIV Clinical Trials | June 18, 2011 | Volume: 12 | Issue: 3 | Pages: 141-150

10.1310/hct1203-141 | PMID 21684854 Get It

Conducting Cancer Control and Survivorship Research via Cooperative Groups: A Report from the American Society of Preventive Oncology
Demark‐Wahnefried, Wendy , Mustian, Karen M. , Minasian, Lori M. , Rowland, Julia, Sprod, Lisa K., Janelsins, Michelle C. , Peppone, Luke J. , Sloan, Jeff A. , Engquist, Karen Basen, Palesh, Oxana Gronskaya , Jones, Lee W. , Buist, Diana S.M. , Paskett, Electra D. , Demark-Wahnefried, Wendy

Cancer Epidemiology, Biomarkers & Prevention | May 5, 2011 | Volume: 20 | Issue: 5 | Pages: 1050-1055

10.1158/1055-9965.epi-11-0176 | PMID 21502540 Get It

Abstract As the number of cancer survivors expands, the need for cancer control and survivorship research becomes increasingly important. The National Cancer Institute (NCI) Cooperative Groups may offer a viable platform to perform such research. Observational, preventive, and behavioral research can often be performed within the cooperative group setting, especially if resources needed for evaluation are fairly simple, if protocols are easily implemented within the typical clinical setting, and if interventions are well standardized. Some protocols are better suited to cooperative groups than are others, and there are advantages and disadvantages to conducting survivorship research within the cooperative group setting. Behavioral researchers currently involved in cooperative groups, as well as program staff within the NCI, can serve as sources of information for those wishing to pursue symptom management and survivorship studies within the clinical trial setting. The structure of the cooperative groups is currently changing, but going forward, survivorship is bound to be a topic of interest and one that perhaps may be more easily addressed using the proposed more centralized structure. Cancer Epidemiol Biomarkers Prev; 20(5); 1050–5. ©2011 AACR.
Array-Based Comparative Genomic Hybridization Identifies CDK4 and FOXM1 Alterations as Independent Predictors of Survival in Malignant Peripheral Nerve Sheath Tum
Yu, Jinsheng , Deshmukh, Hrishikesh , Payton, Jacqueline E. , Scheithauer, Bernd W., Tihan, Tarık , Prayson, Richard A. , Bridge, Julia A. , Ferner, Rosalie E. , Lindberg, Guy, Gutmann, Rebecca J., Emnett, Ryan J., Salavaggione, Lorena, Gutmann, David H. , Nagarajan, Rakesh, Perry, Arie , Dunham, Christopher P. , Guha, Abhijit Ranjan , Watson, Mark A. , Perry, Arie

Clinical Cancer Research | February 16, 2011 | Volume: 17 | Issue: 7 | Pages: 1924-1934

10.1158/1078-0432.ccr-10-1551 | PMID 21325289 Get It

Abstract Purpose: Malignant peripheral nerve sheath tumors (MPNST) are highly aggressive sarcomas with variable patient survival and few known prognostically relevant genomic biomarkers. To identify survival-associated genomic biomarkers, we performed high-resolution array-based comparative genomic hybridization (aCGH) on a large set of MPNSTs. Experimental Design: Candidate gene alterations identified by aCGH in 38 MPNSTs were validated at the DNA, RNA, and protein levels on these same tumors and an independent set of 87 MPNST specimens. Results: aCGH revealed highly complex copy number alterations, including both previously reported and completely novel loci. Four regions of copy number gain were associated with poor patient survival. Candidate genes in these regions include SOX5 (12p12.1), NOL1 and MLF2 (12p13.31), FOXM1 and FKBP1 (12p13.33), and CDK4 and TSPAN31 (12q14.1). Alterations of these candidate genes and several others of interest (ERBB2, MYC and TP53) were confirmed by at least 1 complementary methodology, including DNA and mRNA quantitative real-time PCR, mRNA expression profiling, and tissue microarray-based fluorescence in situ hybridization and immunohistochemistry. Multivariate analysis showed that CDK4 gain/amplification and increased FOXM1 protein expression were the most significant independent predictors for poor survival in MPNST patients (P < 0.05). Conclusions: Our study provides new and independently confirmed candidate genes that could serve as genomic biomarkers for overall survival in MPNST patients. Clin Cancer Res; 17(7); 1924–34. ©2011 AACR.
Development of a Unique Triage System for Acute Care Physical Therapy and Occupational Therapy Services: An Administrative Case Report
Hobbs, Julie, Boysen, Julia, McGarry, Kimberly A., Thompson, Jeffrey M., Nordrum, Jon T.

Physical Therapy | August 6, 2010 | Volume: 90 | Issue: 10 | Pages: 1519-1529

10.2522/ptj.20090166 | PMID 20688874 Get It

Background and PurposeThis administrative case report documents the development of a mechanism by which systematic triage was used to assign patients to therapists in acute care settings. The primary objective was to develop a triage tool to improve patient access to medically necessary therapy services.Case DescriptionA unique triage tool and a decision tree were developed to determine which patients referred to therapists for acute care therapy required skilled services. The triage tool was used to examine therapy referrals for patients from 2 large academic hospitals; 6 criteria were used to determine which evaluations should be cancelled. During the trial period, the predictive ability of individual triage criterion items was analyzed, the tool was modified and validated, and a decision tree was established. Descriptive and chi-square analyses were performed on all variables of interest.OutcomesThe systematic triage system reduced the number of therapy evaluations that were not appropriate by 29%, resulting in an improvement in the availability of therapy services for patients who required skilled care. The average number of patients per therapist per workday decreased from 18.9 to 12.1 and from 15.1 to 12.8 in the 2 hospitals. An improvement in a newly developed “workload index” related to missed patient visits also indicated the success of this project.DiscussionA novel systematic triage system reduced the number of therapy evaluations that were not appropriate, resulting in an improvement in the availability of therapy services for patients who require skilled intervention.
P2‐105: An informant‐based questionnaire for the differential diagnosis of dementia
Parfitt, Francine, Pao, Winnie, Ertekin‐Taner, Nilüfer , Graff‐Radford, Neill R. , Crook, Julia E.

Alzheimer's & Dementia | July 11, 2010 | Volume: 6 | Issue: 4S_Part_11 | Pages: No page available

10.1016/j.jalz.2010.05.1152 Get It