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Arizzi Novelli Alessandra Picone Marco Losso Chiara Volpi Ghirardini Annamaria 《毒物与环境化学》2013,95(4-6):183-191
The aim of this study was to investigate the toxicity of total ammonia towards sea urchin bioassays, in order to elucidate the role of ammonia as confounding factor in sediment quality assessment studies. New toxicity data, expressed as EC50, NOEC and LOEC are reported for Paracentrotus lividus based on experiments at differing pH values. Results confirmed that sperm cell toxicity test is not very sensitive to ammonia, while total ammonia embryotoxicity is strictly pH dependent. Accurate observations of embryotoxic effects at increasing total ammonia concentrations evidenced progressive shifts from malformed plutei to gastrula and blastula blockages. Toxicity data obtained for P. lividus are comparable with previous results with other echinoid species. 相似文献
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Camille Codaccioni Olivier Picone Véronique Lambert Paul Maurice Léo Pomar Norbert Winer Laurent Guibaud Rose-Anne Lavergne Anne-Hélène Saliou Dorothée Quinio Alexandra Benachi Catherine Noel Yves Ville Fabrice Cuillier Christelle Pomares Nicole Ferret Denis Filisetti Anne-Sophie Weingertner Valérie Vequeau-Goua Estelle Cateau Guillaume Benoist Martine Wallon Marc Dommergues Isabelle Villena Laurent Mandelbrot 《黑龙江环境通报》2020,40(13):1741-1752
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Toan Nguyen Solveig Heide Lucie Guilbaud Stéphanie Valence Saskia Vande Perre Eléonore Blondiaux Boris Keren Geneviève Quenum-Miraillet Jean-Marie Jouannic Laurent Mandelbrot Olivier Picone Agnès Guet Vassilis Tsatsaris Mathieu Milh Nadine Girard Marie Vincent Mathilde Nizon Céline Poirsier Alexandre Vivanti Alexandra Benachi Vincent des Portes Laurent Guibaud Olivier Patat Myrtille Spentchian Lisa Frugère Delphine Héron Catherine Garel 《黑龙江环境通报》2023,43(6):746-755
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Cytomegalovirus is the main cause of congenital viral infection and amniotic fluid viral load appears to be the single nonclinical prognostic factor. However, as in other infectious diseases, host genetics may influence the severity of the disease. To test this hypothesis, we looked retrospectively at the fetal gender in cases of severe congenital cytomegalovirus infection in our database. We also analyzed the international English literature covering this subject between 1985 and 2003. The proportion of females with brain abnormalities was statistically different from that of males (62/258: 24% vs 30/251: 12%, p = 0.004). The risk of abnormal brain development in infected fetuses was twice as high in females than in males (Chi2 = 8.7; OR = 2, IC [1.26–3.21]). In our cases, amniotic fluid CMV DNA load was not significantly higher in males than in females (p = 0.06) and was also similar in severely and non-severely infected fetuses (p = 0.09). Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
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Rodrigo Ruano Olivier Picone Alexandra Benachi Anne-Gaelle Grebille Jelena Martinovic Yves Dumez Marc Dommergues 《黑龙江环境通报》2003,23(7):539-542
To illustrate the three-dimensional sonographic features of a rare genetic disorder, we report on prenatal diagnosis of osteogenesis imperfecta congenita associated with encephalocele at 13 weeks of gestation, using conventional and three-dimensional ultrasound. Because the parents were first-degree cousins and on the basis of the family history, a recessive autosomal inheritance was suspected. Of seven previous pregnancies, five were unaffected and two had been terminated in the second trimester owing to a similar abnormality (one affected boy and one affected girl). In the case we present, the diagnosis was made on the basis of two-dimensional ultrasound performed by physicians aware of the history; the quality of three-dimensional ultrasound imaging suggests that this technique might have contributed toward establishing a precise diagnosis in the absence of a positive family history. Besides, the global view provided by three-dimensional surface-rendering images made the parents more confident of the accuracy of the diagnosis. Although osteogenesis imperfecta congenita is generally considered as autosomal dominant, the case we report suggests that it may be inherited in a recessive autosomal fashion at least when associated with encephalocele. Three-dimensional ultrasound confirmed the conventional two-dimensional examination and was helpful in convincing the parents of the accuracy of the diagnosis. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
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