Hakutulokset - Mark Corbett
- Näytetään 1 - 20 yhteensä 59 tuloksesta
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The assessment and appraisal of regenerative medicines and cell therapy products: an exploration of methods for review, economic evaluation and appraisal Tekijä Robert Hettle, Mark Corbett, Sebastian Hinde, Robert Hodgson, Julie Jones-Diette, Nerys Woolacott, Stephen Palmer
Julkaistu 2017Artigo -
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Paternal under-nutrition programs metabolic syndrome in offspring which can be reversed by antioxidant/vitamin food fortification in fathers Tekijä Nicole O. McPherson, Tod Fullston, Wan Xian Kang, Lauren Sandeman, Mark Corbett, Julie A. Owens, Michelle Lane
Julkaistu 2016Artigo -
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Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions Tekijä Mark Corbett, Christel Depienne, Liana Veneziano, Karl Martin Klein, Francesco Brancati, Renzo Guerrini, Federico Zara, Shoji Tsuji, Jozef Gécz
Julkaistu 2023Revisão -
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Acupuncture and other physical treatments for the relief of pain due to osteoarthritis of the knee: network meta-analysis Tekijä Mark Corbett, Stephen Rice, Vichithranie Madurasinghe, Russell Slack, Debra Fayter, Melissa Harden, Alex J. Sutton, Hugh MacPherson, Nerys Woolacott
Julkaistu 2013Revisão -
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Interchromosomal Insertional Translocation at Xq26.3 Alters<i>SOX3</i>Expression in an Individual With XX Male Sex Reversal Tekijä Bryan P. Haines, James Hughes, Mark Corbett, Marie Shaw, Josie Innes, Leena Patel, Jozef Gécz, Jill Clayton‐Smith, Paul Q. Thomas
Julkaistu 2015Artigo -
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Certolizumab pegol and secukinumab for treating active psoriatic arthritis following inadequate response to disease-modifying antirheumatic drugs: a systematic review and economic... Tekijä Mark Corbett, Fadi Chehadah, Mousumi Biswas, Thirimon Moe‐Byrne, Stephen Palmer, Marta Soares, Matthew Walton, Melissa Harden, Pauline Ho, Nerys Woolacott, Laura Bojke
Julkaistu 2017Revisão -
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Tumour necrosis factor-α inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis: a systematic review and economic evaluation Tekijä Mark Corbett, Marta Soares, Gurleen Jhuti, Stephen Rice, Eldon Spackman, E.G. Sideris, Thirimon Moe‐Byrne, Dave Fox, Helena Marzo‐Ortega, Lesley Kay, Nerys Woolacott, Stephen Palmer
Julkaistu 2016Revisão -
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Treatment strategies for new onset atrial fibrillation in patients treated on an intensive care unit: a systematic scoping review Tekijä Laura Drikite, Jonathan Bedford, Liam J. O’Bryan, Tatjana Petrinic, Kim Rajappan, James Doidge, David A Harrison, Kathy Rowan, Paul Mouncey, Duncan Young, Peter Watkinson, Mark Corbett
Julkaistu 2021Artigo -
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Identification of a MicroRNA that Activates Gene Expression by Repressing Nonsense-Mediated RNA Decay Tekijä Ivone G. Bruno, Rachid Karam, Lulu Huang, Anjana Bhardwaj, Chih H. Lou, Eleen Y. Shum, Hye-Won Song, Mark Corbett, Wesley D. Gifford, Jozef Gécz, Samuel L. Pfaff, Miles Wilkinson
Julkaistu 2011Artigo -
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Baseline disease characteristics by surgery history among patients with chronic rhinosinusitis with nasal polyps (CRSwNP) in the global AROMA registry Tekijä Shigeharu Fujieda, Jayant M. Pinto, David W. Jang, Joseph K. Han, James L. Mims, Eugenio De Corso, Martin Wagenmann, Changming Xia, Thomas Plucinak, Mark Corbett, Scott D. Nash, Amr Radwan
Julkaistu 2025Artigo -
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Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations Tekijä Michael Field, Ingrid E. Scheffer, Deepak Gill, Meredith Wilson, Louise Christie, Marie Shaw, Alison Gardner, Georgie C. Glubb, Lynne Hobson, Mark Corbett, Kathryn Friend, Saffron A.G. Willis‐Owen, Jozef Gécz
Julkaistu 2012Artigo -
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Acupuncture for chronic pain and depression in primary care: a programme of research Tekijä Hugh MacPherson, Andrew J. Vickers, Martin Bland, David Torgerson, Mark Corbett, Eldon Spackman, Pedro Saramago, Beth Woods, Helen Weatherly, Mark Sculpher, Andrea Manca, Stewart Richmond, Ann Hopton, Janet Eldred, Ian Watt
Julkaistu 2017Artigo
Työkalut:
Liittyvät aiheet
Biology
Genetics
Gene
Medicine
Internal medicine
Mutation
Epilepsy
Neuroscience
Phenotype
Missense mutation
Psychiatry
Intellectual disability
Pathology
Exome sequencing
Intensive care medicine
Disease
Exome
Genome
MEDLINE
Physical therapy
Psychology
Alternative medicine
Law
Pediatrics
Political science
Randomized controlled trial
Cell
Cell biology
Copy-number variation
DNA sequencing