Identification of variants of the ryanodine receptor type 1 in patients with exertional heat stroke and positive response to the malignant hyperthermia in vitro contracture test
Roux-Buisson, N, Monnier, N, Sagui, E, Abriat, A, Brosset, C, Bendahan, D, Kozak-Ribbens, G, Gazzola, S, Quesada, J.-L., Foutrier-Morello, C, Rendu, J, Figarella-Branger, D, Cozonne, P, Aubert, M, Bourdon, L, Lunardi, J, Fauré, J
Published in British journal of anaesthesia : BJA (01.04.2016)
Published in British journal of anaesthesia : BJA (01.04.2016)
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Journal Article
Modeling of the deep granular bed clogging by nanoparticles
Wingert, L., Bardin-Monnier, N., Charvet, A., Bémer, D., Thomas, D.
Published in Separation and purification technology (01.04.2017)
Published in Separation and purification technology (01.04.2017)
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Journal Article
VECMAtk: a scalable verification, validation and uncertainty quantification toolkit for scientific simulations
Groen, D, Arabnejad, H, Jancauskas, V, Edeling, W N, Jansson, F, Richardson, R A, Lakhlili, J, Veen, L, Bosak, B, Kopta, P, Wright, D W, Monnier, N, Karlshoefer, P, Suleimenova, D, Sinclair, R, Vassaux, M, Nikishova, A, Bieniek, M, Luk, Onnie O, Kulczewski, M, Raffin, E, Crommelin, D, Hoenen, O, Coster, D P, Piontek, T, Coveney, P V
Published in Philosophical transactions of the Royal Society of London. Series A: Mathematical, physical, and engineering sciences (17.05.2021)
Published in Philosophical transactions of the Royal Society of London. Series A: Mathematical, physical, and engineering sciences (17.05.2021)
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Journal Article
Permeability modeling of fibrous media with bimodal fiber size distribution
Gervais, P.-C., Bardin-Monnier, N., Thomas, D.
Published in Chemical engineering science (07.05.2012)
Published in Chemical engineering science (07.05.2012)
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Journal Article
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype
Charignon, D., Ghannam, A., Defendi, F., Ponard, D., Monnier, N., López Trascasa, M., Launay, D., Caballero, T., Djenouhat, K., Fain, O., Cichon, S., Martin, L., Drouet, C.
Published in Allergy (Copenhagen) (01.12.2014)
Published in Allergy (Copenhagen) (01.12.2014)
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Journal Article
Core-rod myopathy caused by mutations in the nebulin gene
Romero, N B, Lehtokari, V-L, Quijano-Roy, S, Monnier, N, Claeys, K G, Carlier, R Y, Pellegrini, N, Orlikowski, D, Barois, A, Laing, N G, Lunardi, J, Fardeau, M, Pelin, K, Wallgren-Pettersson, C
Published in Neurology (06.10.2009)
Published in Neurology (06.10.2009)
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Journal Article
Can bubble columns be an alternative to fibrous filters for nanoparticles collection?
Charvet, A., Bardin-Monnier, N., Thomas, D.
Published in Journal of hazardous materials (15.11.2011)
Published in Journal of hazardous materials (15.11.2011)
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Journal Article
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization
Bevilacqua, J. A., Monnier, N., Bitoun, M., Eymard, B., Ferreiro, A., Monges, S., Lubieniecki, F., Taratuto, A. L., Laquerrière, A., Claeys, K. G., Marty, I., Fardeau, M., Guicheney, P., Lunardi, J., Romero, N. B.
Published in Neuropathology and applied neurobiology (01.04.2011)
Published in Neuropathology and applied neurobiology (01.04.2011)
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Journal Article
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia
Monnier, Nicole, Ferreiro, Ana, Marty, Isabelle, Labarre-Vila, Annick, Mezin, Paulette, Lunardi, Joel
Published in Human molecular genetics (15.05.2003)
Published in Human molecular genetics (15.05.2003)
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Journal Article
Binder liquid distribution during granulation process and its relationship to granule size distribution
Smirani-Khayati, N., Falk, V., Bardin-Monnier, N., Marchal-Heussler, L.
Published in Powder technology (25.10.2009)
Published in Powder technology (25.10.2009)
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Journal Article
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor
MONNIER, Nicole, ROMERO, Norma Beatriz, LERALE, Joëlle, LANDRIEU, Pierre, NIVOCHE, Yves, FARDEAU, Michel, LUNARDI, Joël
Published in Human molecular genetics (15.10.2001)
Published in Human molecular genetics (15.10.2001)
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Journal Article
Correlations between genotype and pharmacological, histological, functional, and clinical phenotypes in malignant hyperthermia susceptibility
Monnier, Nicole, Kozak-Ribbens, Geneviève, Krivosic-Horber, Renée, Nivoche, Yves, Qi, Dong, Kraev, Natasha, Loke, Julian, Sharma, Parveen, Tegazzin, Vincenzo, Figarella-Branger, Dominique, Roméro, Norma, Mezin, Paulette, Bendahan, David, Payen, Jean-François, Depret, Thierry, Maclennan, David H., Lunardi, Joël
Published in Human mutation (01.11.2005)
Published in Human mutation (01.11.2005)
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Journal Article
An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor
MONNIER, Nicole, ROMERO, Norma Beatriz, LERALE, Joëlle, NIVOCHE, Yves, DONG QI, MACLENNAN, David H, FARDEAU, Michel, LUNARDI, Joël
Published in Human molecular genetics (01.11.2000)
Published in Human molecular genetics (01.11.2000)
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Journal Article
G.P.49
Bompaire, F, Roux-Buisson, N, Monnier, N, Feillet, F, Romero, N.B, Laforêt, P, Behin, A
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
G.P.269
Garibaldi, M, Malfatti, E, Brochier, G, Cuisset, J.M, Maurage, C.A, Monnier, N, Eymard, B, Laporte, J, Fardeau, M, Romero, N.B
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
Type III Hereditary Angioedema: First Description of a Mutation in Factor XII Gene and Clinical Features in a Brazilian Family
Moreno, A.S, Valle, S.O.R, Franca, A.T, Levy, S.A, Ponard, D, Monnier, N, Lunardi, J, Arruda, L
Published in Journal of allergy and clinical immunology (01.02.2012)
Published in Journal of allergy and clinical immunology (01.02.2012)
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Journal Article