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Trends in anemia management in US hemodialysis patients 2004-2010. 

Miskulin, Dana C; Zhou, Jing; Tangri, Navdeep; Bandeen-Roche, Karen; Cook, Courtney; Ephraim, Patti L; Crews, Deidra C; ... (13 authors) (BMC Nephrol, 2013-12-01)
BACKGROUND: There have been major changes in the management of anemia in US hemodialysis patients in recent years. We sought to determine the influence of clinical trial results, safety regulations, and changes in reimbursement ...
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Smoking and opioid detoxification: behavioral changes and response to treatment. 

Mannelli, Paolo; Wu, Li-Tzy; Peindl, Kathleen S; Gorelick, David A (Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco, 2013-10)
The relevance of tobacco use in opioid addiction (OA) has generated a demand for available and more effective interventions. Thus, further analysis of less explored nicotine-opioid clinical interactions is warranted.A post-hoc ...
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Variability in performance measures for assessment of hypertension control. 

Navar-Boggan, Ann Marie; Shah, Bimal R; Boggan, Joel C; Stafford, Judith A; Peterson, Eric D (Am Heart J, 2013-05)
BACKGROUND: Definitions of multiple performance measures exist for the assessment of blood pressure control; however, limited data on how these technical variations may affect actual measured performance are available. METHODS: ...
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Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III. 

Sun, Baodong; Fredrickson, Keri; Austin, Stephanie; Tolun, Adviye A; Thurberg, Beth L; Kraus, William E; Bali, Deeksha; ... (9 authors) (Mol Genet Metab, 2013-02)
We investigated the feasibility of using recombinant human acid-α glucosidase (rhGAA, Alglucosidase alfa), an FDA approved therapy for Pompe disease, as a treatment approach for glycogen storage disease type III (GSD III). ...
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Using electronic health records data to assess comorbidities of substance use and psychiatric diagnoses and treatment settings among adults. 

Wu, Li-Tzy; Gersing, Kenneth R; Swartz, Marvin S; Burchett, Bruce; Li, Ting-Kai; Blazer, Dan G (Journal of psychiatric research, 2013-04)
To examine prevalences of substance use disorders (SUD) and comprehensive patterns of comorbidities among psychiatric patients ages 18-64 years (N = 40,099) in an electronic health records (EHR) database.DSM-IV diagnoses ...
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Tobacco use among Asian Americans, Native Hawaiians/Pacific Islanders, and mixed-race individuals: 2002-2010. 

Wu, Li-Tzy; Swartz, Marvin S; Burchett, Bruce; NIDA AAPI Workgroup; Blazer, Dan G (Drug and alcohol dependence, 2013-09)
Non-Hispanic Asian Americans, Native Hawaiians/Pacific Islanders (NHs/PIs), and mixed-race individuals are the fastest growing segments of the US population. We examined prevalences and correlates of tobacco use among these ...
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Hazard-rate analysis and patterns of recurrence in early stage melanoma: moving towards a rationally designed surveillance strategy. 

Salama, April KS; de Rosa, Nicole; Scheri, Randall P; Pruitt, Scott K; Herndon, James E; Marcello, Jennifer; Tyler, Douglas S; ... (8 authors) (PLoS One, 2013)
BACKGROUND: While curable at early stages, few treatment options exist for advanced melanoma. Currently, no consensus exists regarding the optimal surveillance strategy for patients after resection. The objectives of this ...
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Fibroblast growth factor 23 is not associated with and does not induce arterial calcification. 

Scialla, Julia J; Lau, Wei Ling; Reilly, Muredach P; Isakova, Tamara; Yang, Hsueh-Ying; Crouthamel, Matthew H; Chavkin, Nicholas W; ... (23 authors) (Kidney international, 2013-06)
Elevated fibroblast growth factor 23 (FGF23) is associated with cardiovascular disease in patients with chronic kidney disease. As a potential mediating mechanism, FGF23 induces left ventricular hypertrophy; however, its ...
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Skeletal muscle pathology of infantile Pompe disease during long-term enzyme replacement therapy. 

Prater, Sean N; Patel, Trusha T; Buckley, Anne F; Mandel, Hanna; Vlodavski, Eugene; Banugaria, Suhrad G; Feeney, Erin J; ... (9 authors) (Orphanet J Rare Dis, 2013-06-20)
BACKGROUND: Pompe disease is an autosomal recessive metabolic neuromuscular disorder caused by a deficiency of the lysosomal enzyme acid alpha-glucosidase (GAA). It has long been believed that the underlying pathology leading ...
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Algorithm for the early diagnosis and treatment of patients with cross reactive immunologic material-negative classic infantile pompe disease: a step towards improving the efficacy of ERT. 

Banugaria, Suhrad G; Prater, Sean N; Patel, Trusha T; Dearmey, Stephanie M; Milleson, Christie; Sheets, Kathryn B; Bali, Deeksha S; ... (16 authors) (PLoS One, 2013)
OBJECTIVE: Although enzyme replacement therapy (ERT) is a highly effective therapy, CRIM-negative (CN) infantile Pompe disease (IPD) patients typically mount a strong immune response which abrogates the efficacy of ERT, ...
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AuthorWu, Li-Tzy (9)Peterson, Eric D (7)Blazer, Dan G (5)Burchett, Bruce (5)Swartz, Marvin S (5)Fonarow, Gregg C (4)Hernandez, Adrian F (4)Kishnani, Priya S (3)Mannelli, Paolo (3)NIDA AAPI Workgroup (3)... View MoreDate Issued
2013 (32)
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