Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus

M. Grandis; L. Obici; M. Luigetti; C. Briani; F. Benedicenti; G. Bisogni; M. Canepa; F. Cappelli; C. Danesino; G.M. Fabrizi; S. Fenu; G. Ferrandes; C. Gemelli; F. Manganelli; A. Mazzeo; L. Melchiorri; F. Perfetto; L.G. Pradotto; P. Rimessi; G. Tini; S. Tozza; L. Trevisan; D. Pareyson; P. Mandich

doi:10.1186/s13023-020-01633-z

Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus

M. Grandis, L. Obici, M. Luigetti, C. Briani, F. Benedicenti, G. Bisogni, M. Canepa, F. Cappelli, C. Danesino, G.M. Fabrizi, S. Fenu, G. Ferrandes, C. Gemelli, F. Manganelli, A. Mazzeo, L. Melchiorri, F. Perfetto, L.G. Pradotto, P. Rimessi, G. TiniS. Tozza, L. Trevisan, D. Pareyson, P. Mandich

Research output: Contribution to journal › Article › peer-review

Original language	Italian
Journal	Orphanet Journal of Rare Diseases
Volume	15
Issue number	1
DOIs	https://doi.org/10.1186/s13023-020-01633-z
Publication status	Published - 2020

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10.1186/s13023-020-01633-z

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Grandis, M., Obici, L., Luigetti, M., Briani, C., Benedicenti, F., Bisogni, G., Canepa, M., Cappelli, F., Danesino, C., Fabrizi, G. M., Fenu, S., Ferrandes, G., Gemelli, C., Manganelli, F., Mazzeo, A., Melchiorri, L., Perfetto, F., Pradotto, L. G., Rimessi, P., ... Mandich, P. (2020). Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus. Orphanet Journal of Rare Diseases, 15(1). https://doi.org/10.1186/s13023-020-01633-z

Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus. / Grandis, M.; Obici, L.; Luigetti, M.; Briani, C.; Benedicenti, F.; Bisogni, G.; Canepa, M.; Cappelli, F.; Danesino, C.; Fabrizi, G.M.; Fenu, S.; Ferrandes, G.; Gemelli, C.; Manganelli, F.; Mazzeo, A.; Melchiorri, L.; Perfetto, F.; Pradotto, L.G.; Rimessi, P.; Tini, G.; Tozza, S.; Trevisan, L.; Pareyson, D.; Mandich, P.

In: Orphanet Journal of Rare Diseases, Vol. 15, No. 1, 2020.

Research output: Contribution to journal › Article › peer-review

Grandis, M , Obici, L , Luigetti, M, Briani, C, Benedicenti, F, Bisogni, G, Canepa, M, Cappelli, F, Danesino, C, Fabrizi, GM, Fenu, S, Ferrandes, G, Gemelli, C, Manganelli, F, Mazzeo, A, Melchiorri, L, Perfetto, F, Pradotto, LG, Rimessi, P, Tini, G, Tozza, S, Trevisan, L , Pareyson, D & Mandich, P 2020, 'Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus', Orphanet Journal of Rare Diseases, vol. 15, no. 1. https://doi.org/10.1186/s13023-020-01633-z

Grandis, M. ; Obici, L. ; Luigetti, M. ; Briani, C. ; Benedicenti, F. ; Bisogni, G. ; Canepa, M. ; Cappelli, F. ; Danesino, C. ; Fabrizi, G.M. ; Fenu, S. ; Ferrandes, G. ; Gemelli, C. ; Manganelli, F. ; Mazzeo, A. ; Melchiorri, L. ; Perfetto, F. ; Pradotto, L.G. ; Rimessi, P. ; Tini, G. ; Tozza, S. ; Trevisan, L. ; Pareyson, D. ; Mandich, P. / Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus. In: Orphanet Journal of Rare Diseases. 2020 ; Vol. 15, No. 1.

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AU - Obici, L.

AU - Luigetti, M.

AU - Briani, C.

AU - Benedicenti, F.

AU - Bisogni, G.

AU - Canepa, M.

AU - Cappelli, F.

AU - Danesino, C.

AU - Fabrizi, G.M.

AU - Fenu, S.

AU - Ferrandes, G.

AU - Gemelli, C.

AU - Manganelli, F.

AU - Mazzeo, A.

AU - Melchiorri, L.

AU - Perfetto, F.

AU - Pradotto, L.G.

AU - Rimessi, P.

AU - Tini, G.

AU - Tozza, S.

AU - Trevisan, L.

AU - Pareyson, D.

AU - Mandich, P.

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JO - Orphanet Journal of Rare Diseases

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