Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the FERROPORTIN 1 gene (SLC11A3) in a large French-Canadian family by Rivard, Sylvain R, Lanzara, Carmela, Grimard, Doria, Carella, Massimo, Simard, Hervey, Ficarella, Romina, Simard, Raynald, D'Adamo, Adamo Pio, De Braekeleer, Marc, Gasparini, Paolo

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Clinical and Molecular Aspects of Juvenile Hemochromatosis in Saguenay–Lac-Saint-Jean (Quebec, Canada) by Rivard, Sylvain R, Mura, Catherine, Simard, Hervé, Simard, Raynald, Grimard, Doria, Le Gac, Gérald, Raguenes, Odile, Férec, Claude, De Braekeleer, Marc

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Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay–Lac‐Saint‐Jean (Quebec, Canada) by Rivard, Sylvain R., Mura, Catherine, Simard, Hervé, Simard, Raynald, Grimard, Doria, Le Gac, Gérald, Raguenes, Odile, Férec, Claude, De Braekeleer, Marc

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Correlation between mutations and age in cystic fibrosis in a French Canadian population by RIVARD, SYLVAIN R, ALLARD, CHRISTIAN, LEBLANC, JEAN-PIERRE, MILOT, MARCEL, AUBIN, GERVAIS, SIMARD, FERNAND, FÉREC, CLAUDE, DE BRAEKELEER, MARC

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Validation of global moderate-resolution LAI products: a framework proposed within the CEOS land product validation subgroup by Morisette, J.T., Baret, F., Privette, J.L., Myneni, R.B., Nickeson, J.E., Garrigues, S., Shabanov, N.V., Weiss, M., Fernandes, R.A., Leblanc, S.G., Kalacska, M., Sanchez-Azofeifa, G.A., Chubey, M., Rivard, B., Stenberg, P., Rautiainen, M., Voipio, P., Manninen, T., Pilant, A.N., Lewis, T.E., Iiames, J.S., Colombo, R., Meroni, M., Busetto, L., Cohen, W.B., Turner, D.P., Warner, E.D., Petersen, G.W., Seufert, G., Cook, R.

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