1000 resultados para Infants -- Protecció, assistència, etc.
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Provient de la « Bibliothèque de la Chancellerie. »
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Interrogatoires de Guillaume Perrin, procureur au parlement (fol. 1), — Jean Fiot, conseiller (fol. 7), — Pierre « Quarrey, » conseiller (fol. 13), — Jean Pouier, procureur (fol. 33), — Jean Lavisey (fol. 41), — Bénigne Desgaud, receveur de la Sainte-Chapelle (fol. 75), — Jacques La Verne (fol. 107), — etc.
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Contient : « Registre des veux qui furent fais en intencion d'aler sur les Turs, l'an mil quatre cens. chinquante trois, en la presence de très noble et tres redouté prince Phelippe, par la grace de Dieu, duc de Bourgoigne... » ; « Coppie de la bulle donnée l'an lXIII (1463) par le pape Pius [II], et translatée, ce dit an, par solennel orateur l'evesque de Tournay, » G. Filastre ; « Epistre faitte en la contemplacion du saint voyage de Turquie, adreissant à la très crestienne et très heureuse maison de Bourgogne »
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Ex-libris d'A. Kühnholtz-Lordat.
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OBJECTIVE: To describe the epidemiology of chromosomal and non-chromosomal cases of atrioventricular septal defects in Europe. METHODS: Data were obtained from EUROCAT, a European network of population-based registries collecting data on congenital anomalies. Data from 13 registries for the period 2000-2008 were included. RESULTS: There was a total of 993 cases of atrioventricular septal defects, with a total prevalence of 5.3 per 10,000 births (95% confidence interval 4.1 to 6.5). Of the total cases, 250 were isolated cardiac lesions, 583 were chromosomal cases, 79 had multiple anomalies, 58 had heterotaxia sequence, and 23 had a monogenic syndrome. The total prevalence of chromosomal cases was 3.1 per 10,000 (95% confidence interval 1.9 to 4.3), with a large variation between registers. Of the 993 cases, 639 cases were live births, 45 were stillbirths, and 309 were terminations of pregnancy owing to foetal anomaly. Among the groups, additional associated cardiac anomalies were most frequent in heterotaxia cases (38%) and least frequent in chromosomal cases (8%). Coarctation of the aorta was the most common associated cardiac defect. The 1-week survival rate for live births was 94%. CONCLUSION: Of all cases, three-quarters were associated with other anomalies, both chromosomal and non-chromosomal. For infants with atrioventricular septal defects and no chromosomal anomalies, cardiac defects were often more complex compared with infants with atrioventricular septal defects and a chromosomal anomaly. Clinical outcomes for atrioventricular septal defects varied between regions. The proportion of termination of pregnancy for foetal anomaly was higher for cases with multiple anomalies, chromosomal anomalies, and heterotaxia sequence.
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Contient : Épitaphes des Cordeliers de Neufchâteau ; Épitaphes de Bayon ; Épitaphes de l'abbaye de Beaupré ; Épitaphes de Magnières ; Épitaphes des Cordeliers de Mirecourt ; Épitaphes des Carmes de Besançon ; Épitaphes des Cordeliers de Besançon ; Épitaphes de Bourbonne ; Épitaphes de l'abbaye de Morimond ; Épitaphes de Beaufrémont ; Épitaphes de Remennecourt ; Copie abrégée de l'épitomé de Jean Daucy ; Extrait du Trésor de l'évêché de Verdun