Zobrazeno 1 - 10 of 75 pro vyhledávání: '"E, Cochet"'
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2
Eosinophilic Esophagitis with Dysphagia and Food Impaction in a Young Adult
Autor: Anthony A Cochet, James M Francis, Allyson E Cochet
Publikováno v: Aerospace Medicine and Human Performance. 86:742-746
Background Eosinophilic esophagitis (EoE) is an emerging esophageal disease associated with dysphagia and food impaction. Practice guidelines have only recently been developed. It affects 1/1000 individuals, predominantly young men. As this demograph
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaf9300b28ee77e37634473121402f21
https://doi.org/10.3357/amhp.4236.2015
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3
The prevalence of NAFLD and NASH among patients with psoriasis in a tertiary care dermatology and rheumatology clinic
Autor: P. J. Brown, P. B. Lamb, E. M. Brunt, D. F. Battafarano, A. E. Cochet, K. K. Roberts, Stephen A. Harrison
Publikováno v: Alimentary Pharmacology & Therapeutics. 41:293-300
SummaryBackground Psoriasis has been linked to metabolic syndrome and non-alcoholic fatty liver disease (NAFLD). Data suggest that the prevalence of NAFLD is increased in patients with psoriasis. The aim of this study was to determine the prevalence
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38b1365c7bdf37a4bdfdb0f39c6621f7
https://doi.org/10.1111/apt.13042
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5
FSHD myoblasts fail to downregulate intermediate filament protein vimentin during myogenic differentiation
Autor: Yegor S. Vassetzky, Petr Dmitriev, Vasily Ogryzko, M. Lipinski, E. Cochet, Dalila Laoudj-Chenivesse, Ana Barat
Publikováno v: Biopolymers and Cell, Vol 27, Iss 5, Pp 359-363 (2011)
Scopus-Elsevier
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant hereditary neuromuscular disorder. The clinical features of FSHD include weakness of the facial and shoulder girdle muscles followed by wasting of skeletal muscles of the pelvic g
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b17fa6b46a98fd5fa6fc519c7d914e8
http://biopolymers.org.ua/archive/2011/05/08.pdf
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6
Mutations in the autoinflammatory cryopyrin-associated periodic syndrome gene: epidemiological study and lessons from eight years of genetic analysis in France
Autor: L, Cuisset, I, Jeru, B, Dumont, A, Fabre, E, Cochet, J, Le Bozec, M, Delpech, S, Amselem, I, Touitou, R, Touraine
Publikováno v: Annals of the Rheumatic Diseases. 70:495-499
BackgroundCryopyrin-associated periodic syndromes (CAPS) consist of a continuum of autoinflammatory diseases caused by a defect in interleukin 1β regulation. Although symptoms may vary widely, the discovery, in 2001, of the gene involved (NLRP3) has
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e61af0d1cc6d985b6880a91189c133d1
https://doi.org/10.1136/ard.2010.138420
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7
Cochlear implantation: a bionic system to restore hearing in severely hearing impaired patients
Autor: P H, Van de Heyning, K, Vermeire, E, Cochet, A, Hofkens, M, De Bodt
Publikováno v: Verhandelingen - Koninklijke Academie voor Geneeskunde van Belgie. 66(4)
CI replaces and functionally bypasses the inner haircells of the cochlea. Candidate selection is not merely based on non-aided auditory thresholds, but aided speech recognition tests in quite and in noise after a rehabilitation period may be decisive
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2d3815c28f872087799d1aa9a630fb88
https://pubmed.ncbi.nlm.nih.gov/15553098
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