998 resultados para Patin, Guy, 1601-1672


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« Copie faite sur l'imprimé, à Pézenas, l'an 1676 ; « avec notes de Charles d'Hozier et de d'Hozier de Sérigny (1756). — Il y a une table alphabétique des noms en tête du volume.

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Preuves de noblesse de Charles de Montsaunin (1), — et de dom François de Calvo (4 et 6), pour les Ordres du roi ; — de Marie-Jeanne-Françoise d'Alesso d'Eragni (8), — des demoiselles Marie et Louise Lois de Boussens (10), — d'Anne Raimond de Villogon (12), — Marie-Françoise de Saint-Martin (16), — Barbe de Limosin d'Alheim (18), — Marie-Louise de Houlei (20), pour Saint-Cyr ; — de Charles Acary de La Suze (22), — Pierre de Brie (24), — Joseph-Emmanuel d'Orillac (27), — François-Jacques Petit de La Borde (29). — Jean-Joseph de Rastel de Rocheblave (33), — Charles de Fautereau (39), — Pierre de Baud du Castelet (41), pour l'École militaire. — Parchemin. — Blasons peints. Épreuves de gravure des « Statuts de l'Ordre du St-Esprit. De l'Imprimerie royale, 1703 » (fol. 43). « Généalogie de la maison de Noailles » (fol. 56), avec nombreux dessins, blasons et encadrements, au crayon.

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Copie, faite pour Gaignières, du ms. français 25204, provenant de St-Victor. — Blasons peints.

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Contient : « Ordonnances de l'Ordre de la Toison d'or » ; « Traicté d'armes » ; « Aultre institution d'officiers d'armes » ; « Comment l'on doibt faire et eslire ung Empereur » ; « Copie de la lettre d'ordonnance et fondation de la chapelle des roys d'armes... de France, fondée en l'église de M. St Antoine le Petit, à Paris. » (1406.) — Copies de Ph. Laurens. XXXII (31843). « Gentilitia nobilissimi... Ordinis Transisvlaniae, invictissimorum Saliorum et Francorum genitricis, ex vetustissimis monumentis eruta,... opera A. v. M. » ; « Description de la noblesse de Hollande »

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Contient : I Recherche de la noblesse de la Généralité de Caen, par d'Aligre (1634-1635) ; II Recherche de la noblesse de la Généralité de Rouen, par Jacques Barin, marquis de La Galissonnière (1666-1682)

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The shrews of the Sorex araneus group, characterized by the sexual chromosome complex XY1, Y2 have been intensively studied by morphological, karyotypical, and biochemical analyses. Nevertheless, the phylogenetic relationships among the species belonging to the araneus complex are still under debate, as different approaches gave often contradictory results. In this paper, partial nucleotide sequences of the mitochondrial DNA cytochrome b gene (1011 bp) were determined for 6 species of the araneus group from Eurasia and North America. We also included in the data set the sequences of Sorex samniticus, whose relationships with the araneus group remain controversial. Three other species representing two major karyological groups were also examined. Both parsimony and distance trees strongly support the monophyly of the araneus group. Sorex sumniticus is significantly more closely related to the araneus complex than to the other species included in the analysis. Based on the branching pattern within the araneus group, an attempt has been made to reconstruct the colonization history of the Holarctic region.

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This corrects the article on p. e73445 in vol. 8.]. This corrects the article "Topographical Body Fat Distribution Links to Amino Acid and Lipid Metabolism in Healthy Non-Obese Women" , e73445. There was an error in the title of the article. The correct version of the title in the article is: Topographical Body Fat Distribution Links to Amino Acid and Lipid Metabolism in Healthy Obese Women The correct citation is: Martin F-PJ, Montoliu I, Collino S, Scherer M, Guy P, et al. (2013) Topographical Body Fat Distribution Links to Amino Acid and Lipid Metabolism in Healthy Obese Women. PLoS ONE 8(9): e73445. doi:10.1371/journal.pone.0073445

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We compared the extent and origin of muscle fatigue induced by short-pulse-low-frequency [conventional (CONV)] and wide-pulse-high-frequency (WPHF) neuromuscular electrical stimulation. We expected CONV contractions to mainly originate from depolarization of axonal terminal branches (spatially determined muscle fiber recruitment) and WPHF contractions to be partly produced via a central pathway (motor unit recruitment according to size principle). Greater neuromuscular fatigue was, therefore, expected following CONV compared with WPHF. Fourteen healthy subjects underwent 20 WPHF (1 ms-100 Hz) and CONV (50 μs-25 Hz) evoked isometric triceps surae contractions (work/rest periods 20:40 s) at an initial target of 10% of maximal voluntary contraction (MVC) force. Force-time integral of the 20 evoked contractions (FTI) was used as main index of muscle fatigue; MVC force loss was also quantified. Central and peripheral fatigue were assessed by voluntary activation level and paired stimulation amplitudes, respectively. FTI in WPHF was significantly lower than in CONV (21,717 ± 11,541 vs. 37,958 ± 9,898 N·s P<0,001). The reductions in MVC force (WPHF: -7.0 ± 2.7%; CONV: -6.2 ± 2.5%; P < 0.01) and paired stimulation amplitude (WPHF: -8.0 ± 4.0%; CONV: -7.4 ± 6.1%; P < 0.001) were similar between conditions, whereas no change was observed for voluntary activation level (P > 0.05). Overall, our results showed a different motor unit recruitment pattern between the two neuromuscular electrical stimulation modalities with a lower FTI indicating greater muscle fatigue for WPHF, possibly limiting the presumed benefits for rehabilitation programs.