Burden of Illness for Patients with familial amyloidotic Polyneuropathy (Fap) Begins Early and Increases with Disease Progression von Denoncourt, R.N, Adams, D, Coelho, T, Bettencourt, B.R, Plaisted, A, Amitay, O, Falzone, R, Harrop, J, White, L, De Frutos, R, Cehelsky, J, Nochur, S, Vaishnaw, A.K, Gollob, J

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The V122I mutation in hereditary transthyretin-mediated amyloidosis is significantly associated with an increased incidence of polyneuropathy von Parker, M.M, Damrauer, S.M, Erbe, D, Aldinc, E, Ticau, S, Flynn-Carroll, A, Deaton, A.M, Ward, L.D, Rader, D.J, Fitzgerald, K, Vaishnaw, A.K, Hinkle, G, Nioi, P

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PND52 - Burden of Illness for Patients with familial amyloidotic Polyneuropathy (Fap) Begins Early and Increases with Disease Progression von Denoncourt, R.N., Adams, D., Coelho, T., Bettencourt, B.R., Plaisted, A., Amitay, O., Falzone, R., Harrop, J., White, L., De Frutos, R., Cehelsky, J., Nochur, S., Vaishnaw, A.K., Gollob, J.

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Transcriptional regulation of the human C4 gene von Mitchell, T.J., Vaishnaw, A.K., Rose, J., Walport, M.J., Morley, B.J.

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DNase I hypersensitivity mapping and promoter polymorphism analysis of human C4 von Vaishnaw, A K, Hargreaves, R, Campbell, R D, Morley, B J, Walport, M J

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Progress in the delivery of siRNA therapeutics: Potential in uveal melanoma von Gollob, J.A., Bumcrot, D., Toudjarska, I., Bastian, B.C., Sah, D.W., Vaishnav, A.K.

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