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Lista de resultados: 41-50 de um total de 161 resultados (tempo de pesquisa: 0.015 segundos).
DataTítuloAutor(es)TipoAcesso
2019Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathyFeichtinger, René G.; Mucha, Bettina E.; Hengel, Holger; Orfi, Zakaria; Makowski, Christine; Dort, Junio; D'Anjou, Guy; Nguyen, Thi Tuyet Mai; Buchert, Rebecca; Juenger, Hendrik; Freisinger, Peter; Baumeister, Sarah; Schoser, Benedikt; Ahting, Uwe; Keimer, Reinhard; Nguyen, Cam-Tu Emilie; Fabre, Paul; Gauthier, Julie; Miguet, Marguerite; Lopes, Fátima; AlHakeem, Afnan; AlHashem, Amal; Tabarki, Brahim; Kandaswamy, Krishna Kumar; Bauer, Peter; Steinbacher, Peter; Prokisch, Holger; Sturm, Marc; Strom, Tim M.; Ellezam, Benjamin; Mayr, Johannes A.; Schöls, Ludger; Michaud, Jacques L.; Campeau, Philippe M.; Haack, Tobias B.; Dumont, Nicolas A.ArtigoAcesso restrito autor
Nov-2019CECDAIic - a new useful tool in pan-intestinal evaluation of Crohn's disease patients in the era of mucosal healingArieira, Cátia; Magalhães, Rui; Dias de Castro, Francisca; Boal Carvalho, Pedro; Rosa, Bruno; Moreira, Maria João; Cotter, José Almeida BerkeleyArtigoAcesso restrito autor
2019p.G360R Is a Pathogenic GLA Gene Mutation Responsible for a Classic Phenotype of Fabry DiseaseCarvalho Silva, Daniela Marisa; Marques, Nuno; Azevedo, Olga; Miltenberger-Miltenyi, Gabriel; Bento, Dina; Guedes, João; Azevedo, Pedro; Bispo, João; Mota, Teresa; Fernandes, Raquel; Nzwalo, Hipólito; Cabrita, Ana; Ramos, André; de Jesus, IlídioArtigoAcesso restrito autor
2019Discordance between old and new criteria for stratifying patients with COPDAraújo, António Manuel Silva Duarte de; Teixeira, Pedro Miguel Silva Costa Afonso; Hespanhol, Venceslau; Correia de Sousa, JaimeCarta ao editorAcesso aberto
Set-2019Engineering of human cardiac muscle electromechanically matured to an adult-like phenotypeRonaldson-Bouchard, Kacey; Yeager, Keith; Teles, Diogo; Chen, Timothy; Ma, Stephen; Song, LouJin; Morikawa, Kumi; Wobma, Holly M.; Ruiz, Edward C.; Yazawa, Masayuki; Vunjak-Novakovic, GordanaArtigoAcesso aberto
Nov-2019Mutational profile of driver genes in Brazilian melanomasVicente, Anna Luiza S. A.; Crovador, Camila S.; Macedo, Graziela; Scapulatempo-Neto, Cristovam; Reis, R. M.; Vazquez, Vinicius L.ArtigoAcesso aberto
Ago-2019Therapeutic thrombocytapheresis for extreme thrombocytosis after chemotherapy in essential thrombocytosisDias, Ana Raquel Pereira Vieira Almeida; Garrote, Marta; Cid, Joan; Mustieles, Maria-Jesús; Alba, Cristina; Lozano, MiquelArtigoAcesso restrito UMinho
Mai-2011Toward a model-based predictive controller design in brain-computer interfacesKamrunnahar, M.; Dias, Nuno Sérgio Mendes; Schiff, S. J.ArtigoAcesso aberto
Abr-2011Prostate cancer in Cowden syndrome: somatic loss and germline mutation of the PTEN geneBarbosa, Mafalda Fernanda Cabral Santos; Henrique, Martinha; Pinto-Basto, Jorge; Claes, Kathleen; Soares, GabrielaCarta ao editorAcesso restrito UMinho
1-Mar-2018Predictability of tunnel depth for intrastromal corneal ring segments implantation between manual and Femtosecond laser techniquesMonteiro, Tiago; Alfonso, José F.; Franqueira, Nuno; Faria-Correia, Fernando; Ambrósio, Renato; Madrid-Costa, DavidArtigoAcesso restrito UMinho