Éditeur(s) : Agencia tip. de F. Diaz de Leon Agencia tip. de F. Diaz de Leon ( México )
Résumé : Altamirano, F. Historia natural aplicada de los antiguos mexicanos.--Sánchez, J. Importancia de la historia natural en el estudio de la historia antigua y de la arqueología americanas.--Álvarez y Guerrero, L.G. Estudio filológico comparativo entre los idiomas náhuatl y huaxteco.--Martínez Gracida, M. Minería y su industria; páginas de la obra inédita "Los Indios oaxaqueños y sus monumentos arqueológicos."--Adam, L. Esquisse grammaticale et vocabulaire de la langue guaraouno.--Grasserie, R. de la. Langue auca; vocabulaire, fragments de grammaire, textes, inédits.
America
America

002819024
22578332
ANU7549
07025128

Éditeur(s) : Archives départementales de la Martinique
Résumé : Le Marquis de Bouillé, 12 février 1782
5Fi92
Saint-Christophe

Droits : Reproduction soumise à autorisation
http://www.patrimoines-martinique.org/ark:/35569/a011414681896ZaQsvn

Éditeur(s) : Archives de la Martinique
15Fi74
Saint-Christophe

Droits : Reproduction soumise à autorisation des Archives de la Martinique
http://www.patrimoines-martinique.org/ark:/35569/a011470672738wYUXDu

Éditeur(s) : Lee and Shepard Lee and Shepard ( Boston (10 Milk St.) )
Résumé : Some ill. by R.P. Leitch and T. MacQuoid; engraving by Butterworth & Heath, W.J. Linton, R.S. Marriott, Morison, W.L. Thomas, Wentworth, and Williamson.
Originally published as The Children's Robinson Crusoe by Mrs. Eliza Farrar in 1830.
This edition omits "most of the chapter relating to the early life of the hero, and condenses the rest of the volume." It is adapted "to the use of schools ... by simplifying many words and reducing the length of sentences. With these exceptions, the editor has taken few liberties with the text of Mrs. Farrar."--P. 3.
Based upon part I of Daniel Defoe's Robinson Crusoe.
Publisher's advertisement p. 4 of cover.
(Statement of Responsibility) by a Lady ; edited and adapted by William T. Adams.
United States of America -- Massachusetts -- Boston

Droits : This item is presumed to be in the public domain. The University of Florida George A. Smathers Libraries respect the intellectual property rights of others and do not claim any copyright interest in this item. Users of this work have responsibility for determining copyright status prior to reusing, publishing or reproducing this item for purposes other than what is allowed by fair use or other copyright exemptions. Any reuse of this item in excess of fair use or other copyright exemptions may require permission of the copyright holder. The Smathers Libraries would like to learn more about this item and invite individuals or organizations to contact The Department of Special and Area Studies Collections (special@uflib.ufl.edu) with any additional information they can provide.
SN01270
27081349

Éditeur(s) : HAL CCSD
Résumé : International audience
Objective To guide nosology and classification of patients with eosinophilic granulomatosis with polyangiitis (EGPA) based on phenotype and presence or absence of ANCA. Methods Organ manifestations and ANCA status were retrospectively analyzed based on the presence or not of predefined definite vasculitis features or surrogates of vasculitis in patients asthma, eosinophilia, and at least one systemic organ manifestation attributable to systemic disease. Results The study population included 157 patients (mean age 49.4 ± 14.1), with a follow-up of 7.4 ± 6.4 years. Patients with ANCA (31%) more frequently had weight loss, myalgias, arthralgias, biopsy-proven vasculitis, glomerulonephritis on biopsy, hematuria, leukocytoclastic capillaritis and/or eosinophilic infiltration of arterial wall on biopsy, and other renal disease. A total of 41% of patients had definite vasculitis manifestations (37%) or strong surrogates of vasculitis (4%), of whom only 53% had ANCA. Mononeuritis multiplex was associated with systemic vasculitis (p = 0.005) and with the presence of ANCA (p < 0.001). Overall, 59% of patients had polyangiitis as defined by definite vasculitis, strong surrogate of vasculitis, mononeuritis multiplex, and/or ANCA with at least one systemic manifestation other than ENT or respiratory. Patients with polyangiitis had more systemic manifestations including arthralgias (p = 0.02) and renal disease (p = 0.024), had higher peripheral eosinophilia (p = 0.027), and a trend towards less myocarditis (p = 0.057). Using predefined criteria of vasculitis and surrogates of vasculitis, ANCA alone were found to be insufficient to categorise patients with vasculitis features. Conclusion We suggest a revised nomenclature and definition for EGPA and a new proposed entity referred to as hypereosinophilic asthma with systemic (non vasculitic) manifestations. © 2016 Elsevier B.V.
Autoimmunity Reviews

hal-01467544
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01467544
DOI : 10.1016/j.autrev.2016.09.018
PUBMED : 27671089