1. Repositório Científico do Centro Hospitalar do Porto

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Results 1-10 of 11 (Search time: 0.001 seconds).
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Issue DateTitleAuthor(s)TypeAccess Type
2014Vitreous Amyloidosis as the Presenting Symptom of Familial Amyloid Polyneuropathy TTR Val30Met in a Portuguese PatientSeca, M.; Ferreira, N.; Coelho, T.articleopenAccess
2013Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathyCoelho, T.; Maia, L.; Martins-Silva, A.; Cruz, M.; Planté-Bordeneuve, V.; Suhr, O.; Conceição, I.; Schmidt, H.; Trigo, P.; Kelly, J.; Labaudinière, R.; Chan, J.; Packman, J.; Grogan, D.articleopenAccess
2014Prevalence of use of preimplantation genetic diagnosis in Unidade Clínica de Paramiloidose from Centro Hospitalar do PortoValdrez, K.; Alves, E.; Coelho, T.; Silva, S.articleopenAccess
2013Guideline of transthyretin-related hereditary amyloidosis for cliniciansAndo, Y.; Coelho, T.; Berk, J.; Cruz, M.; Ericzon, B.; Ikeda, S.; Lewis, W.; Obici, L.; Planté-Bordeneuve, V.; Rapezzi, C.; Said, G.; Salvi, F.articleopenAccess
2015Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose studySuhr, O.; Coelho, T.; Buades, J.; Pouget, J.; Conceicao, I.; Berk, J.; Schmidt, H.; Waddington-Cruz, M.; Campistol, J.; Bettencourt, B.; Vaishnaw, A.; Gollob, J.; Adams, D.articleopenAccess
2017Familial amyloid polyneuropathy in Portugal: New genes modulating age-at-onsetSantos, D.; Coelho, T.; Alves-Ferreira, M.; Sequeiros, J.; Mendonça, D.; Alonso, I.; Lemos, C.; Sousa, A.articleopenAccess
Jun-2016Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin AmyloidosisCoelho, T.; Merlini, G.; Bulawa, C.; Fleming, J.; Judge, D.; Kelly, J.; Maurer, M.; Planté-Bordeneuve, V.; Labaudinière, R.; Mundayat, R.; Riley, S.; Lombardo, I.; Huertas, P.articleopenAccess
2016Peripheral Blood Cell Gene Expression Diagnostic for Identifying Symptomatic Transthyretin Amyloidosis Patients: Male and Female Specific SignaturesKurian, S.; Novais, M.; Whisenant, T.; Gelbart, T.; Buxbaum, J.; Kelly, J.; Coelho, T.; Salomon, D.articleopenAccess
2017Trial design and rationale for APOLLO, a Phase 3, placebo-controlled study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathyAdams, D.; Suhr, O.; Dyck, P.; Litchy, W.; Leahy, R.; Chen, J.; Gollob, J.; Coelho, T.articleopenAccess
3-Oct-2017Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin GeneGonçalves, A.; Oliveira, J.; Coelho, T.; Taipa, R.; Melo-Pires, M.; Sousa, M.; Santos, R.articleopenAccess

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