Your browser doesn't support javascript.
loading
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.
Afiliação
  • Grandis M; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal and Child Health (DINOGMI), Section of Medical Genetics, University of Genoa, c/o DIMI Viale Benedetto XV, 6, 16132, Genova, Italy.
  • Obici L; IRCCS Policlinico San Martino, Genova, Italy.
  • Luigetti M; Amyloidosis Research and Treatment Center, IRCCS Fondazione Policlinico San Matteo, Pavia, Italy.
  • Briani C; UOC Neurologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Benedicenti F; Università Cattolica del Sacro Cuore, Rome, Italy.
  • Bisogni G; Department of Neuroscience, University of Padova, Padova, Italy.
  • Canepa M; Medical Genetics, Azienda Sanitaria Dell'Alto Adige, Bolzano, Italy.
  • Cappelli F; Centro Clinico Nemo Adulti-Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
  • Danesino C; Cardiovascular Disease Unit, IRCCS Policlinico San Martino, Genova, and IRCCS Italian Cardiovascular Network, Department of Internal Medicine, University of Genova, Genova, Italy.
  • Fabrizi GM; Tuscan Regional Amyloidosis Center, Careggi University Hospital, Firenze, Italy.
  • Fenu S; Molecular Medicine Department, University of Pavia, Pavia, Italy.
  • Ferrandes G; Department of Neurosciences, Biomedicine and Movement Sciences, Section of Neurology, University of Verona and University Hospital GB Rossi, Verona, Italy.
  • Gemelli C; Unit of Rare Neurodegenerative and Neurometabolic Diseases, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • Manganelli F; IRCCS Policlinico San Martino, Genova, Italy.
  • Mazzeo A; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal and Child Health (DINOGMI), Section of Medical Genetics, University of Genoa, c/o DIMI Viale Benedetto XV, 6, 16132, Genova, Italy.
  • Melchiorri L; Neuromuscular Omnicentre (NEMO)-Fondazione Serena Onlus, Arenzano, GE, Italy.
  • Perfetto F; Department of Neuroscience, Reproductive and Odontostomatological Sciences, University of Naples "Federico II", Napoli, Italy.
  • Pradotto LG; Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
  • Rimessi P; Medical Genetics Unit, Azienda Ospedaliero Universitaria Di Ferrara, Ferrara, Italy.
  • Tini G; Tuscan Regional Amyloidosis Center, Careggi University Hospital, Firenze, Italy.
  • Tozza S; Department of Neurosciences, University of Turin, Torino, Italy.
  • Trevisan L; Division of Neurology and Neurorehabilitazion, IRCCS Istituto Auxologico Italiano, Piancavallo, VB, Italy.
  • Pareyson D; Medical Genetics Unit, Azienda Ospedaliero Universitaria Di Ferrara, Ferrara, Italy.
  • Mandich P; Cardiovascular Disease Unit, IRCCS Policlinico San Martino, Genova, and IRCCS Italian Cardiovascular Network, Department of Internal Medicine, University of Genova, Genova, Italy.
Orphanet J Rare Dis ; 15(1): 348, 2020 12 14.
Article em En | MEDLINE | ID: mdl-33317601
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropatias Amiloides Familiares Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropatias Amiloides Familiares Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article