Search Results - "Joseph, Patricia M"

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  1. 1

    Review of the abdominal manifestations of cystic fibrosis in the adult patient by Robertson, Michael B, Choe, Kyuran A, Joseph, Patricia M

    Published in Radiographics (01-05-2006)
    “…Cystic fibrosis is a common inherited fatal disease. As the life expectancy of affected individuals continues to increase with advances in disease management,…”
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    Journal Article
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    Shared Decision-Making Tool for Self-Management of Home Therapies for Patients With Cystic Fibrosis by Eckman, Mark H., Kopras, Elizabeth J., Montag-Leifling, Karen, Kirby, Lari P., Burns, Lisa, Indihar, Veronica M., Joseph, Patricia M.

    Published in MDM policy & practice (2017)
    “…Objective: Patients with cystic fibrosis (CF) undertake time-consuming programs of home therapies. Our objective was to develop a tool to help CF patients…”
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    A kindred of children with interstitial lung disease by Thomas, Heather, Risma, Kimberly A, Graham, T Brent, Brody, Alan S, Deutsch, Gail H, Young, Lisa R, Joseph, Patricia M

    Published in Chest (01-07-2007)
    “…Childhood interstitial lung disease (ILD) is a spectrum of diseases including many different rare lung conditions. We present a family with an unusual…”
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    Adults with cystic fibrosis: spiritual coping with lifelong disease by Grossoehme, Daniel H., Cole, Adam G., Lewis, Katrina, Stamper, Sophia M., Teeters, Alexis, Joseph, Patricia M.

    Published in Journal of health care chaplaincy (02-04-2020)
    “…Cystic fibrosis (CF) is a chronic life-shortening disease requiring significant coping. Spiritual belief relates to treatment behaviors. Little is known about…”
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    Randomized trial of biofilm testing to select antibiotics for cystic fibrosis airway infection by Moskowitz, Samuel M., Emerson, Julia C., McNamara, Sharon, Shell, Richard D., Orenstein, David M., Rosenbluth, Daniel, Katz, Marcia F., Ahrens, Richard, Hornick, Douglas, Joseph, Patricia M., Gibson, Ronald L., Aitken, Moira L., Benton, Wade W., Burns, Jane L.

    Published in Pediatric pulmonology (01-02-2011)
    “…Rationale In cystic fibrosis (CF), conventional antibiotic susceptibility results correlate poorly with clinical outcomes. We hypothesized that biofilm testing…”
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    Changes in Mineral Micronutrient Status During and After Pulmonary Exacerbation in Adults With Cystic Fibrosis by Lee, Moon Jeong, Alvarez, Jessica A., Smith, Ellen M., Killilea, David W., Chmiel, James F., Joseph, Patricia M., Grossmann, Ruth E., Gaggar, Amit, Ziegler, Thomas R., Tangpricha, Vin

    Published in Nutrition in clinical practice (01-12-2015)
    “…Background: Patients with cystic fibrosis (CF) may be at risk for micronutrient depletion, particularly during periods of illness and infection. The purpose of…”
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    Using Spirituality After an Adult CF Diagnosis: Cognitive Reframing and Adherence Motivation by Grossoehme, Daniel H., Ragsdale, Judith R., Cotton, Sian, Meyers, Melenie A., Clancy, John P., Seid, Michael, Joseph, Patricia M.

    Published in Journal of health care chaplaincy (01-07-2012)
    “…Chronic illness is a significant stressor; the majority of Americans cope utilizing spirituality. Numerous studies demonstrate links between spiritual coping…”
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    Aerosol and lobar administration of a recombinant adenovirus to individuals with cystic fibrosis. I. Methods, safety, and clinical implications by Joseph, P M, O'Sullivan, B P, Lapey, A, Dorkin, H, Oren, J, Balfour, R, Perricone, M A, Rosenberg, M, Wadsworth, S C, Smith, A E, St George, J A, Meeker, D P

    Published in Human gene therapy (20-07-2001)
    “…Cystic fibrosis (CF), an autosomal recessive disorder resulting from mutations in the cystic fibrosis trans-membrane conductance regulator (CFTR) gene, is the…”
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    Aerosol and lobar administration of a recombinant adenovirus to individuals with cystic fibrosis. II. Transfection efficiency in airway epithelium by Perricone, M A, Morris, J E, Pavelka, K, Plog, M S, O'Sullivan, B P, Joseph, P M, Dorkin, H, Lapey, A, Balfour, R, Meeker, D P, Smith, A E, Wadsworth, S C, St George, J A

    Published in Human gene therapy (20-07-2001)
    “…A phase I clinical trial was conducted in which recombinant adenovirus containing the cystic fibrosis trans-membrane regulator (CFTR) (Ad2/CFTR) was…”
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    Cystic Fibrosis Pulmonary Guidelines: Pulmonary Complications: Hemoptysis and Pneumothorax by FLUME, Patrick A, MOGAYZEL, Peter J, ROBINSON, Karen A, ROSENBLATT, Randall L, QUITTELL, Lynne, MARSHALL, Bruce C

    “…Cystic fibrosis (CF) is a recessive genetic disease characterized by dehydration of the airway surface liquid and impaired mucociliary clearance. As a result,…”
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    Inhibitory Effect of Heparin on Serotonin-induced Hyperplasia and Hypertrophy of Smooth Muscle Cells by Lee, Sheu-Ling, Wang, Wei-Wei, Joseph, Patricia M, Hales, Charles A, Fanburg, Barry L

    “…Serotonin (5-HT) produces both hyperplastic and hypertrophic effects on smooth muscle cell (SMC) in culture. Heparin is known to inhibit serum-induced…”
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    Case 45-1993: A 23-Year-Old Asthmatic Man with Pulmonary Infiltrates and Hilar Lymphadenopathy by Joseph, Patricia M, Mark, Eugene J

    Published in The New England journal of medicine (11-11-1993)
    “…Presentation of Case A 23-year-old man with asthma was admitted to the hospital because of an increased cough with pulmonary infiltrates. There was a history…”
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    Review of the Abdominal Manifestations of Cystic Fibrosis in the Adult Patient1 by Michael B. Robertson, Kyuran A. Choe, Patricia M. Joseph

    Published in Radiographics (01-05-2006)
    “…Cystic fibrosis is a common inherited fatal disease. As the life expectancy of affected individuals continues to increase with advances in disease management,…”
    Get full text
    Journal Article
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    The role of Na+/H+ exchange and growth factors in pulmonary artery smooth muscle cell proliferation by Quinn, D A, Dahlberg, C G, Bonventre, J P, Scheid, C R, Honeyman, T, Joseph, P M, Thompson, B T, Hales, C A

    “…Chronic hypoxia produces pulmonary hypertension, in part because of hypertrophy and hyperplasia of pulmonary artery smooth muscle cells (PA SMC)…”
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    Inhibition of hypoxic pulmonary hypertension by heparins of differing in vitro antiproliferative potency by Thompson, B T, Spence, C R, Janssens, S P, Joseph, P M, Hales, C A

    “…Heparin inhibits smooth-muscle cell (SMC) growth in vitro and inhibits the development of hypoxic pulmonary hypertension and vascular remodeling in vivo. We…”
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    Differential effect of three commercial heparins on Na+/H+ exchange and growth of PASMC by Dahlberg, C G, Thompson, B T, Joseph, P M, Garg, H G, Spence, C R, Quinn, D A, Bonventre, J V, Hales, C A

    Published in The American journal of physiology (01-02-1996)
    “…Heparin preparations vary in chemical content and in antiproliferative activity for pulmonary artery smooth muscle cells (PASMC). Intracellular alkalinization…”
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