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pro vyhledávání: '"C. Castellan"'
Akademický článek
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Autor:
E. Molteni, C. Pirone, F. Ceccarelli, C. Castellani, C. Alessandri, M. Di Franco, V. Riccieri, F.R. Spinelli, R. Priori, R. Scrivo, F. Conti
Publikováno v:
Reumatismo, Vol 76, Iss 2 (2024)
Objective. Data from trials demonstrated that abatacept (ABA) has a good safety and efficacy profile in treating rheumatoid arthritis. We have studied the retention rate of ABA in a real-life cohort of patients with rheumatoid arthritis. Methods. T
Externí odkaz:
https://doaj.org/article/15a0aa3db02c49159c824c94d7a3941b
Publikováno v:
European Journal of Public Health. 29
Background The whole-school approach focuses on promoting health and wellbeing for pupils, employees, and parents. In Norway, several schools are now developing such an approach and opening the school premises for community activities. The aim of thi
Autor:
Flávia Gonçalves, Antonio Carlos Bombana, C. Castellan, Carlos Eduardo Francci, Roberto Ruggiero Braga, Soraia de Fátima Carvalho Souza
Publikováno v:
International Endodontic Journal. 42:867-873
Aim To compare two resin-based root canal sealers (AH Plus and dual cure Epiphany) in terms of flow, polymerization stress and bond strength to dentine. Methodology Flow was evaluated by measuring the diameter of uncured discs of sealer (0.5 mL) afte
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype
Autor:
Heather Woodward, Christine Klein, Claudio C. Castellan, Xandra O. Breakefield, Joanne Leung, Peter P. Pramstaller, Patricia L. Kramer, Monika Scherer, Bernhard Kis, Peter Vieregge, Laurie J. Ozelius, Martin Kann, Curtis C. Page
Publikováno v:
Annals of Neurology. 48:65-71
A gene for autosomal recessive parkinsonism, PARK2 (parkin), has recently been identified on chromosome 6q and shown to be mutated in Japanese and European families, mostly with early-onset parkinsonism. Here we present a large pedigree from South Ty
Autor:
Xandra O. Breakefield, Laurie J. Ozelius, Christine Klein, Patricia L. Kramer, Claudio C. Castellan, Peter P. Pramstaller
Publikováno v:
Annals of Neurology. 44:394-398
The gene causing early-onset torsion dystonia (DYT1) has recently been identified, and two new dystonia genes, one for adult-onset focal dystonia (DYT7) and one for a mixed dystonia phenotype (DYT6), have been mapped. We evaluated clinically a family
Autor:
Corrado Angelini, Chiara Fritegotto, F Benedicenti, Franco Stanzial, A Cristofoletti, Marina Fanin, Enrico Peterle, C Castellan, A. C. Nascimbeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::898343afd5f2e1c56275c813d2b6da2b
http://hdl.handle.net/11577/3353760
http://hdl.handle.net/11577/3353760
Publikováno v:
Human genetics. 126(2)
Autor:
A. Lajoinie, B Kassai, L. El-Amrani, S. Malik, Y. Mimouni, N. Paret, C. Castellan, K. An Nguyen, C. Carcel, L. Milliat-Guittard
Publikováno v:
Revue d'Épidémiologie et de Santé Publique. 63:S77
Introduction L’incidence des effets indesirables medicamenteux (EIM) chez les enfants hospitalises est de 9,5 % [6,81 ; 12,26] avec un taux d’EIM graves de 12,3 % [8,43 ; 16,7]. Peu d’etudes ont demontre que la prescription hors AMM est signifi
Autor:
AM Schott, C. Castellan, Ka Nguyen, A. Lajoinie, N. Paret, B Kassai, S. Malik, Y. Mimouni, L. Milliat-Guittard, L. El-Amrani, Thierry Vial
Publikováno v:
Archives of Disease in Childhood. 99:A62.2-A62
Background and aim To date few studies have shown a significant association between the off-label drug use and adverse drug reactions. (ADRs). The main aims of this study are to evaluate the relationship between adverse drug reactions and unlicensed