Zobrazeno 1 - 10
of 164
pro vyhledávání: '"Kaminsky , Pierre"'
Autor:
Bassez, G., Bedat-Millet, A.-L., Behin, A., Eymard, B., Leonard-Louis, S., Stojkovic, T., Canal, A., Decostre, V., Bouhour, F., Boyer, F., Caillaud, C., Castaing, Y., Chapon, F., Cintas, P., Durieu, I., Echaniz-Laguna, A., Feasson, L., Ferrer, X., Froissart, R., Piraud, M., Germain, D., Benistan, K., Guffon-Fouilhoux, N., Journel, H., Labauge, P., Levy, A., Magot, A., Péréon, Y., Minot-Myhié, M.-C., Nadaj-Pakleza, A., Nathier, C., Pellegrini, N., Petiot, P., Lofaso, F., Dutry, A., Renard, D., Sacconi, S., Desnuelle, C., Salort-Campana, E., Pouget, J., Tiffreau, V., Vincent, D., Zagnoli, F., Papadopoulos, Constantinos, Orlikowski, David, Prigent, Hélène, Lacour, Arnaud, Tard, Céline, Furby, Alain, Praline, Julien, Solé, Guilhem, Hogrel, Jean-Yves, De Antonio, Marie, Semplicini, Claudio, Deibener-Kaminsky, Joelle, Kaminsky, Pierre, Eymard, Bruno, Taouagh, Nadjib, Perniconi, Barbara, Hamroun, Dalil, Laforêt, Pascal
Publikováno v:
In Molecular Genetics and Metabolism September 2017 122(1-2):80-85
Autor:
Poussel, Mathias *, Thil, Catherine, Kaminsky, Pierre, Mercy, Magalie, Gomez, Emmanuel, Chaouat, Ari, Chabot, François, Chenuel, Bruno
Publikováno v:
In Neuromuscular Disorders May 2015 25(5):403-408
Autor:
Kaminsky, Pierre, Lidove, Olivier
Publikováno v:
In La Presse Médicale November 2014 43(11):1174-1184
Autor:
Poussel, Mathias, Kaminsky, Pierre, Renaud, Pierre, Laroppe, Julien, Pruna, Lelia, Chenuel, Bruno
Publikováno v:
In Respiratory Physiology & Neurobiology 1 March 2014 193:43-51
Akademický článek
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Publikováno v:
In La Presse Medicale September 2013 42(9) Part 1:e281-e284
Autor:
Zuily, Stéphane, Regnault, Véronique, Guillemin, Francis, Kaminsky, Pierre, Rat, Anne-Christine, Lecompte, Thomas, Wahl, Denis
Publikováno v:
In Thrombosis Research July 2013 132(1):e1-e7
Publikováno v:
In International Journal of Cardiology 20 January 2013 162(3):172-178
Publikováno v:
In Clinical Neurology and Neurosurgery July 2011 113(6):464-468
Autor:
Stirnemann Jérôme, Vigan Marie, Hamroun Dalil, Heraoui Djazia, Rossi-Semerano Linda, Berger Marc G, Rose Christian, Camou Fabrice, de Roux-Serratrice Christine, Grosbois Bernard, Kaminsky Pierre, Robert Alain, Caillaud Catherine, Froissart Roselyne, Levade Thierry, Masseau Agathe, Mignot Cyril, Sedel Frédéric, Dobbelaere Dries, Vanier Marie T, Valayanopoulos Vassili, Fain Olivier, Fantin Bruno, de Villemeur Thierry, Mentré France, Belmatoug Nadia
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 77 (2012)
Abstract Background Clinical features, complications and treatments of Gaucher’s disease (GD), a rare autosomal–recessive disorder due to a confirmed lysosomal enzyme (glucocerebrosidase) deficiency, are described. Methods All patients with known
Externí odkaz:
https://doaj.org/article/d6f365a1e786437fa298ec7657985b69