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  1. AU=Freeman Richard B Jr
  2. AU="Wang, Qi-En"
  3. AU="Mallamaci, M"
  4. AU="Turk, Yael R"
  5. AU="Tinto, Monica"
  6. AU="Selvendiran, Karuppaiyah" AU="Selvendiran, Karuppaiyah"
  7. AU="Enns, Murray W"
  8. AU="Yaohua Yang" AU="Yaohua Yang"

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  1. Artikel ; Online: Bone alterations of pamidronate therapy in children with cerebral palsy complicating orthopedic management.

    Almeida Da Silva, Luiz Carlos / Kaymaz, Burak / Hori, Yusuke / Montufar Wright, Parma E / Rogers, Kenneth J / Trionfo, Arianna / Howard, Jason J / Bowen, J Richard / Shrader, M Wade / Miller, Freeman

    Journal of pediatric orthopedics. Part B

    2023  

    Abstract: Cerebral palsy (CP) is a heterogeneous group of disorders with different clinical types and underlying genetic variants. Children with CP are at risk for fragility fractures secondary to low bone mineral density, and although bisphosphonates are ... ...

    Abstract Cerebral palsy (CP) is a heterogeneous group of disorders with different clinical types and underlying genetic variants. Children with CP are at risk for fragility fractures secondary to low bone mineral density, and although bisphosphonates are prescribed for the treatment of children with bone fragility, there is limited information on long-term bone impact and safety. Children with CP usually present overtubulated bones, and the thickening of cortical bone by pamidronate treatment can potentially further narrow the medullary canal. Our purpose was to report bone alterations attributable to pamidronate therapy that impact orthopedic care in children with CP. The study consisted of 41 children with CP treated with pamidronate for low bone mineral density from 2006 to 2020. Six children presented unique bone deformities and unusual radiologic features attributed to pamidronate treatment, which affected their orthopedic care. The cases included narrowing of the medullary canal and sclerotic bone, atypical femoral fracture, and heterotopic ossification. Treatment with bisphosphonate reduced the number of fractures from 101 in the pretreatment period to seven in the post-treatment period (P < 0.001). In conclusion, children with CP treated with bisphosphonate have a reduction in low-energy fractures; however, some fractures still happen, and pamidronate treatment can lead to bone alterations including medullary canal narrowing with sclerotic bone and atypical femoral fractures. In very young children, failure to remodel may lead to thin, large femoral shafts with cystic medullary canals. More widespread use of bisphosphonates in children with CP may make these bone alterations more frequent. Level of evidence: Level IV: Case series with post-test outcomes.
    Sprache Englisch
    Erscheinungsdatum 2023-10-09
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 1473-5865
    ISSN (online) 1473-5865
    DOI 10.1097/BPB.0000000000001136
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Insomnia as a mediating therapeutic target for depressive symptoms: A sub-analysis of participant data from two large randomized controlled trials of a digital sleep intervention.

    Henry, Alasdair L / Miller, Christopher B / Emsley, Richard / Sheaves, Bryony / Freeman, Daniel / Luik, Annemarie I / Littlewood, Donna L / Saunders, Kate E A / Kanady, Jennifer C / Carl, Jenna R / Davis, Michelle L / Kyle, Simon D / Espie, Colin A

    Journal of sleep research

    2020  Band 30, Heft 1, Seite(n) e13140

    Abstract: Insomnia predicts the onset of depression, commonly co-presents with depression and often persists following depression remission. However, these conditions can be challenging to treat concurrently using depression-specific therapies. Cognitive ... ...

    Abstract Insomnia predicts the onset of depression, commonly co-presents with depression and often persists following depression remission. However, these conditions can be challenging to treat concurrently using depression-specific therapies. Cognitive behavioural therapy for insomnia may be an appropriate treatment to improve both insomnia and depressive symptoms. We examined the effects of a fully-automated digital cognitive behavioural therapy intervention for insomnia (Sleepio) on insomnia and depressive symptoms, and the mediating role of sleep improvement on depressive symptoms in participants from two randomized controlled trials of digital cognitive behavioural therapy for insomnia. We also explored potential moderators of intervention effects. All participants met criteria for probable insomnia disorder and had clinically significant depressive symptomatology (PHQ-9 ≥ 10; n = 3,352). Individuals allocated to treatment in both trials were provided access to digital cognitive behavioural therapy. Digital cognitive behavioural therapy significantly improved insomnia (p < .001; g = 0.76) and depressive symptoms (p < .001; g = 0.48) at post-intervention (weeks 8-10), and increased the odds (OR = 2.9; 95% CI = 2.34, 3.65) of clinically significant improvement in depressive symptoms (PHQ-9 < 10). Improvements in insomnia symptoms at mid-intervention mediated 87% of the effects on depressive symptoms at post-intervention. No variables moderated effectiveness outcomes, suggesting generalizability of these findings. Our results suggest that effects of digital cognitive behavioural therapy for insomnia extend to depressive symptoms in those with clinically significant depressive symptomatology. Insomnia may, therefore, be an important therapeutic target to assist management of depressive symptoms.
    Mesh-Begriff(e) Cognitive Behavioral Therapy/methods ; Depression/complications ; Female ; Humans ; Male ; Randomized Controlled Trials as Topic ; Sleep Initiation and Maintenance Disorders/psychology ; Treatment Outcome
    Sprache Englisch
    Erscheinungsdatum 2020-08-18
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1122722-9
    ISSN 1365-2869 ; 0962-1105
    ISSN (online) 1365-2869
    ISSN 0962-1105
    DOI 10.1111/jsr.13140
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: Evidence

    Blasi, Joseph R / Freeman, Richard B / Kruse, Douglas L

    The Oxford handbook of mutual, co-operative, and co-owned business , p. 211-226

    what the US research shows about worker ownership

    2017  , Seite(n) 211–226

    Verfasserangabe Joseph R. Blasi, Richard B. Freeman, and Douglas L. Kruse
    Sprache Englisch
    Verlag Oxford University Press
    Erscheinungsort Oxford, United Kingdom
    Dokumenttyp Artikel
    ISBN 978-0-19-968497-7 ; 0-19-968497-9
    Datenquelle ECONomics Information System

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  4. Artikel: Employee stock ownership and profit sharing in the new era of financialization and inequality in the distribution of capital income

    Blasi, Joseph R / Freeman, Richard B / Kruse, Douglas L

    Inequality, uncertainty, and opportunity : the varied and growing role of finance and labour relations , p. 225-246

    2015  , Seite(n) 225–246

    Verfasserangabe Joseph R. Blasi (Rutgers University), Richard B. Freeman (Harvard University), Douglas L. Kruse (Rutgers University)
    Schlagwörter Mitarbeiterkapitalbeteiligung ; Erfolgsbeteiligung ; Einkommensverteilung ; Vermögensverteilung ; USA
    Sprache Englisch
    Verlag Labor and Employment Relations Association
    Erscheinungsort Champaign, IL
    Dokumenttyp Artikel
    ISBN 978-0-913447-10-9 ; 0-913447-10-2
    Datenquelle ECONomics Information System

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  5. Artikel ; Online: Aim2 suppresses cigarette smoke-induced neutrophil recruitment, neutrophil caspase-1 activation and anti-Ly6G-mediated neutrophil depletion.

    Donovan, Chantal / Kim, Richard Y / Galvao, Izabela / Jarnicki, Andrew G / Brown, Alexandra C / Jones-Freeman, Bernadette / Gomez, Henry M / Wadhwa, Ridhima / Hortle, Elinor / Jayaraman, Ranjith / Khan, Haroon / Pickles, Sophie / Sahu, Priyanka / Chimankar, Vrushali / Tu, Xiaofan / Ali, Md Khadem / Mayall, Jemma R / Nguyen, Duc H / Budden, Kurtis F /
    Kumar, Vinod / Schroder, Kate / Robertson, Avril Ab / Cooper, Matthew A / Wark, Peter Ab / Oliver, Brian G / Horvat, Jay C / Hansbro, Philip M

    Immunology and cell biology

    2022  Band 100, Heft 4, Seite(n) 235–249

    Abstract: Increased inflammasome responses are strongly implicated in inflammatory diseases; however, their specific roles are incompletely understood. Therefore, we sought to examine the roles of nucleotide-binding oligomerization domain-like receptor (NLR) ... ...

    Abstract Increased inflammasome responses are strongly implicated in inflammatory diseases; however, their specific roles are incompletely understood. Therefore, we sought to examine the roles of nucleotide-binding oligomerization domain-like receptor (NLR) family, pyrin domain-containing 3 (NLRP3) and absent in melanoma-2 (AIM2) inflammasomes in cigarette smoke-induced inflammation in a model of experimental chronic obstructive pulmonary disease (COPD). We targeted NLRP3 with the inhibitor MCC950 given prophylactically or therapeutically and examined Aim2
    Mesh-Begriff(e) Animals ; Caspase 1 ; Cigarette Smoking/adverse effects ; DNA-Binding Proteins ; Mice ; Mice, Inbred C57BL ; Neutrophil Infiltration ; Neutrophils
    Chemische Substanzen Aim2 protein, mouse ; DNA-Binding Proteins ; Caspase 1 (EC 3.4.22.36)
    Sprache Englisch
    Erscheinungsdatum 2022-03-21
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 284057-1
    ISSN 1440-1711 ; 0818-9641
    ISSN (online) 1440-1711
    ISSN 0818-9641
    DOI 10.1111/imcb.12537
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Buch: The citizen's share

    Blasi, Joseph R / Freeman, Richard B / Kruse, Douglas L

    putting ownership back into democracy

    2013  

    Verfasserangabe Joseph R. Blasi; Richard B. Freeman; Douglas L. Kruse
    Schlagwörter Employee ownership ; Mitarbeiterkapitalbeteiligung ; USA
    Sprache Englisch
    Umfang 293 S., graph. Darst.
    Verlag Yale Univ. Press
    Erscheinungsort New Haven, Conn. u.a.
    Dokumenttyp Buch
    Anmerkung Includes bibliographical references and index
    ISBN 9780300192254 ; 0300192258
    Datenquelle ECONomics Information System

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  7. Artikel ; Online: Critical role for iron accumulation in the pathogenesis of fibrotic lung disease.

    Ali, Md Khadem / Kim, Richard Y / Brown, Alexandra C / Donovan, Chantal / Vanka, Kanth S / Mayall, Jemma R / Liu, Gang / Pillar, Amber L / Jones-Freeman, Bernadette / Xenaki, Dikaia / Borghuis, Theo / Karim, Rafia / Pinkerton, James W / Aryal, Ritambhara / Heidari, Moones / Martin, Kristy L / Burgess, Janette K / Oliver, Brian G / Trinder, Debbie /
    Johnstone, Daniel M / Milward, Elizabeth A / Hansbro, Philip M / Horvat, Jay C

    The Journal of pathology

    2020  Band 251, Heft 1, Seite(n) 49–62

    Abstract: Increased iron levels and dysregulated iron homeostasis, or both, occur in several lung diseases. Here, the effects of iron accumulation on the pathogenesis of pulmonary fibrosis and associated lung function decline was investigated using a combination ... ...

    Abstract Increased iron levels and dysregulated iron homeostasis, or both, occur in several lung diseases. Here, the effects of iron accumulation on the pathogenesis of pulmonary fibrosis and associated lung function decline was investigated using a combination of murine models of iron overload and bleomycin-induced pulmonary fibrosis, primary human lung fibroblasts treated with iron, and histological samples from patients with or without idiopathic pulmonary fibrosis (IPF). Iron levels are significantly increased in iron overloaded transferrin receptor 2 (Tfr2) mutant mice and homeostatic iron regulator (Hfe) gene-deficient mice and this is associated with increases in airway fibrosis and reduced lung function. Furthermore, fibrosis and lung function decline are associated with pulmonary iron accumulation in bleomycin-induced pulmonary fibrosis. In addition, we show that iron accumulation is increased in lung sections from patients with IPF and that human lung fibroblasts show greater proliferation and cytokine and extracellular matrix responses when exposed to increased iron levels. Significantly, we show that intranasal treatment with the iron chelator, deferoxamine (DFO), from the time when pulmonary iron levels accumulate, prevents airway fibrosis and decline in lung function in experimental pulmonary fibrosis. Pulmonary fibrosis is associated with an increase in Tfr1
    Mesh-Begriff(e) Airway Remodeling/drug effects ; Animals ; Bleomycin/pharmacology ; Cell Proliferation ; Cells, Cultured ; Extracellular Matrix/drug effects ; Extracellular Matrix/pathology ; Fibroblasts/drug effects ; Fibroblasts/pathology ; Humans ; Idiopathic Pulmonary Fibrosis/drug therapy ; Idiopathic Pulmonary Fibrosis/metabolism ; Idiopathic Pulmonary Fibrosis/pathology ; Iron/metabolism ; Lung/drug effects ; Lung/pathology ; Macrophages/drug effects ; Macrophages/pathology ; Mice, Knockout
    Chemische Substanzen Bleomycin (11056-06-7) ; Iron (E1UOL152H7)
    Sprache Englisch
    Erscheinungsdatum 2020-03-30
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3119-7
    ISSN 1096-9896 ; 0022-3417
    ISSN (online) 1096-9896
    ISSN 0022-3417
    DOI 10.1002/path.5401
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel: Composition and Drivers of Gut Microbial Communities in Arctic-Breeding Shorebirds.

    Grond, Kirsten / Santo Domingo, Jorge W / Lanctot, Richard B / Jumpponen, Ari / Bentzen, Rebecca L / Boldenow, Megan L / Brown, Stephen C / Casler, Bruce / Cunningham, Jenny A / Doll, Andrew C / Freeman, Scott / Hill, Brooke L / Kendall, Steven J / Kwon, Eunbi / Liebezeit, Joseph R / Pirie-Dominix, Lisa / Rausch, Jennie / Sandercock, Brett K

    Frontiers in microbiology

    2019  Band 10, Seite(n) 2258

    Abstract: Gut microbiota can have important effects on host health, but explanatory factors and pathways that determine gut microbial composition can differ among host lineages. In mammals, host phylogeny is one of the main drivers of gut microbiota, a result of ... ...

    Abstract Gut microbiota can have important effects on host health, but explanatory factors and pathways that determine gut microbial composition can differ among host lineages. In mammals, host phylogeny is one of the main drivers of gut microbiota, a result of vertical transfer of microbiota during birth. In birds, it is less clear what the drivers might be, but both phylogeny and environmental factors may play a role. We investigated host and environmental factors that underlie variation in gut microbiota composition in eight species of migratory shorebirds. We characterized bacterial communities from 375 fecal samples collected from adults of eight shorebird species captured at a network of nine breeding sites in the Arctic and sub-Arctic ecoregions of North America, by sequencing the V4 region of the bacterial 16S ribosomal RNA gene. Firmicutes (55.4%), Proteobacteria (13.8%), Fusobacteria (10.2%), and Bacteroidetes (8.1%) dominated the gut microbiota of adult shorebirds. Breeding location was the main driver of variation in gut microbiota of breeding shorebirds (
    Sprache Englisch
    Erscheinungsdatum 2019-10-09
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2587354-4
    ISSN 1664-302X
    ISSN 1664-302X
    DOI 10.3389/fmicb.2019.02258
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: Model for end-stage liver disease (MELD) exception guidelines.

    Wiesner, Russell / Lake, John R / Freeman, Richard B / Gish, Robert G

    Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society

    2006  Band 12, Heft 12 Suppl 3, Seite(n) S85–7

    Mesh-Begriff(e) Humans ; Liver Failure/surgery ; Liver Transplantation ; Models, Biological ; Practice Guidelines as Topic ; Resource Allocation ; Severity of Illness Index ; Tissue and Organ Procurement
    Sprache Englisch
    Erscheinungsdatum 2006-12
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Practice Guideline
    ZDB-ID 2006866-9
    ISSN 1527-6473 ; 1527-6465
    ISSN (online) 1527-6473
    ISSN 1527-6465
    DOI 10.1002/lt.20961
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Cutaneous Melanoma, Version 2.2019, NCCN Clinical Practice Guidelines in Oncology.

    Coit, Daniel G / Thompson, John A / Albertini, Mark R / Barker, Christopher / Carson, William E / Contreras, Carlo / Daniels, Gregory A / DiMaio, Dominick / Fields, Ryan C / Fleming, Martin D / Freeman, Morganna / Galan, Anjela / Gastman, Brian / Guild, Valerie / Johnson, Douglas / Joseph, Richard W / Lange, Julie R / Nath, Sameer / Olszanski, Anthony J /
    Ott, Patrick / Gupta, Aparna Priyanath / Ross, Merrick I / Salama, April K / Skitzki, Joseph / Sosman, Jeffrey / Swetter, Susan M / Tanabe, Kenneth K / Wuthrick, Evan / McMillian, Nicole R / Engh, Anita M

    Journal of the National Comprehensive Cancer Network : JNCCN

    2019  Band 17, Heft 4, Seite(n) 367–402

    Abstract: The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Cutaneous melanoma have been significantly revised over the past few years in response to emerging data on immune checkpoint inhibitor therapies and BRAF-targeted therapy. This ... ...

    Abstract The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Cutaneous melanoma have been significantly revised over the past few years in response to emerging data on immune checkpoint inhibitor therapies and BRAF-targeted therapy. This article summarizes the data and rationale supporting extensive changes to the recommendations for systemic therapy as adjuvant treatment of resected disease and as treatment of unresectable or distant metastatic disease.
    Mesh-Begriff(e) Humans ; Medical Oncology/standards ; Melanoma/diagnosis ; Skin Neoplasms/diagnosis ; Melanoma, Cutaneous Malignant
    Sprache Englisch
    Erscheinungsdatum 2019-02-28
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Practice Guideline
    ZDB-ID 2250759-0
    ISSN 1540-1413 ; 1540-1405
    ISSN (online) 1540-1413
    ISSN 1540-1405
    DOI 10.6004/jnccn.2019.0018
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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