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1 Ergebnisse
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Clinical and genetic profile of patients enrolled in the Tr..:
Dispenzieri, Angela
;
Coelho, Teresa
;
Conceição, Isabel
...
Orphanet Journal of Rare Diseases, 1750-1172, 2022, 17:1,. , 2022
Link:
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-20331
RT Journal T1
Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS) : 14-year update
UL https://suche.suub.uni-bremen.de/peid=base-ftumeauniv:oai:DiVA.org:umu-203317&Exemplar=1&LAN=DE A1 Dispenzieri, Angela A1 Coelho, Teresa A1 Conceição, Isabel A1 Waddington-Cruz, Márcia A1 Wixner, Jonas A1 Kristen, Arnt V A1 Rapezzi, Claudio A1 Planté-Bordeneuve, Violaine A1 Gonzalez-Moreno, Juan A1 Maurer, Mathew S A1 Grogan, Martha A1 Chapman, Doug A1 Amass, Leslie A1 Pavia, Pablo Garcia A1 Tarnev, Ivaylo A1 Costello, Jose Gonzalez A1 Briseno, Maria Alejandra Gonzalez Duarte A1 Schmidt, Hartmut A1 Drachman, Brian A1 Barroso, Fabio Adrian A1 Yamashita, Taro A1 Lairez, Olivier A1 Sekijima, Yoshiki A1 Vita, Giuseppe A1 Jeon, Eun-Seok A1 Hanna, Mazen A1 Slosky, David A1 Luigetti, Marco A1 LoRusso, Samantha A1 Beamud, Francisco Munoz A1 Adams, David A1 Moelgaard, Henning A1 Press, Rayomand A1 Cirami, Calogero Lino A1 Nienhuis, Hans A1 Plana, Josep Maria Campistol A1 Inamo, Jocelyn A1 Jacoby, Daniel A1 Emdin, Michele A1 Quan, Dianna A1 Hummel, Scott A1 Witteles, Ronald A1 Dori, Amir A1 Shah, Sanjiv A1 Lenihan, Daniel A1 Azevedo, Olga A1 Murali, Srinivas A1 Zivkovic, Sasa A1 Low, Soon Chai A1 Nativi-Nicolau, Jose A1 Fine, Nowell A1 Tallaj, Jose A1 Tschoepe, Carsten A1 Torrón, Roberto Fernandéz A1 Polydefkis, Michael A1 Merlini, Giampaolo A1 Badelita, Sorina A1 Gottlieb, Stephen A1 Tauras, James A1 Correia, Edileide Barros A1 Ventura, Hector A1 Gess, Burkhard A1 Darstein, Felix A1 Oh, Jeeyoung A1 Marburger, Tessa A1 Van Cleemput, Johan A1 Salutto, Valeria Lujan A1 Parman, Yesim A1 Chao, Chi-Chao A1 Sarswat, Nitasha A1 Mueller, Christopher A1 Steidley, David A1 Ralph, Jeffrey A1 Warner, Alberta A1 Cotts, William A1 Hoffman, James A1 Rugiero, Marcelo A1 Misawa, Sonoko A1 Blanco, Jose Luis Munoz A1 Davila, Lucia Galan A1 Sadeh, Menachem A1 Luo, Jin A1 Kyriakides, Theodoros A1 Wang, Annabel A1 Kaufmann, Horacio PB Umeå universitet, Avdelningen för medicin; Division of Hematology, Mayo Clinic, MN, Rochester, United States; Unidade Corino Andrade, Hospital Santo António, Centro Hospitalar Universitário do Porto, Porto, Portugal; Department of Neurosciences, CHULN, Hospital de Santa Maria, Universidade de Lisboa, Lisbon, Portugal; University Hospital, Federal University of Rio de Janeiro, National Amyloidosis Referral Center, CEPARM, Rio de Janeiro, Brazil; Department of Cardiology, Angiology, Respiratory Medicine, Medical University of Heidelberg, Heidelberg, Germany; Cardiological Centre, University of Ferrara, Ferrara, Italy; Maria Cecilia Hospital, GVM Care & Research, Cotignola, Ravenna, Italy; Hôpital Henri Mondor – AP-HP, East Paris University, Créteil, France; Servicio de Medicina Interna, Hospital Universitario Son Llatzer, Instituto de Investigación Sanitaria Illes Balears, Palma de Mallorca, Spain; Columbia University College of P... YR 2022 K1 Amyloidosis K1 Cardiomyopathy K1 Polyneuropathy K1 Registry K1 Transthyretin K1 Neurology K1 Neurologi JF Orphanet Journal of Rare Diseases, 1750-1172, 2022, 17:1, LK http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-203317 DO http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-203317 SF ELIB - SuUB Bremen
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