Browsing by Author Hawkins, Philip N.
Showing results 1 to 3 of 3
Issue Date | Title | Author(s) |
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1996 | Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene. | Booth, David R.; Tan, Si-Yen; Booth, Sussanne E.; Tennent, Glenys A.; Hutchinson, Winston L.; Hsuan, J. Justin; Totty, Nicholas F.; Truong, Oanh; Soutar, Anne K.; Hawkins, Philip N.; Bruguera i Cortada, Miquel, 1942-; Caballeria Rovira, Joan; Solé, Manel; Campistol Plana, Josep M.; Pepys, Mark B. |
5-Jul-2018 | Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis | Campistol Plana, Josep M.; González Duarte, Alejandra; Suhr, Ole B.; Goyal, Sunita; Gandhi, Pritesh J.; Polydefkis, Michael; Sekijima, Yoshiki; O'Riordan, William D.; Yang, Chih-Chao; Ueda, Mitsuharu; Kristen, Arnt V.; Coelho, Teresa; Berk, John L.; Lin, Kon Ping; Vita, Giuseppe; Attarian, Shahram; Planté Bordeneuve, Violaine; Mezei, Michelle M.; Buades, Juan; Brannagan, Thomas H.; Kim, Byoung J.; Oh, Jeeyoung; Parman, Yesim; Hawkins, Philip N.; Solomon, Scott D.; Dyck, Peter J.; Chen, Jihong; Strahs, Andrew L.; Nochur, Saraswathy V.; Sweetser, Marianne T.; Garg, Pushkal P.; Vaishnaw, Akshay K.; Gollob, Jared A. |
21-Aug-2013 | The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry | Lachmann, Helen J.; Papa, R.; Gerhold, K.; Obici, Laura; Touitou, I.; Cantarini, Luca; Frenkel, Joost; Antón López, Jordi; Koné-Paut, Isabelle; Cattalini, Marco; Bader-Meunier, B.; Insalaco, Antonella; Hentgen, Veronique; Merino, R.; Modesto, Consuelo; Toplak, N.; Berendes, R.; Ozen, Seza; Cimaz, Rolando; Jansson, Annette F.; Brogan, Paul; Hawkins, Philip N.; Ruperto, N.; Martini, Alberto; Woo, Patricia; Gattorno, Marco |