Zobrazeno 1 - 10
of 218
pro vyhledávání: '"A.-L. Delezoide"'
Autor:
Azzedine Aboura, Emmanuel Spaggiari, Martine Sinico, Céline Dupont, A. L. Delezoide, Philippe Mabboux, Fabien Guimiot
Publikováno v:
European Journal of Medical Genetics. 55:498-501
Saethre-Chotzen syndrome is a craniosynostosis syndrome that is rarely diagnosed prenatally. It is caused by cytogenetic deletions or mutations of the TWIST1 gene. We report here a de novo prenatal case with clinically and molecularly well defined Sa
Publikováno v:
Revue de médecine périnatale. 3:86-95
La dysgenesie tubulaire renale (DTR) et l’exposition antenatale aux antagonistes du recepteur de l’angiotensine 2 (ARA2) alterent le developpement renal fœtal causant anurie et oligoamnios. Le tableau classique associe hypoplasie de la voute cr
Publikováno v:
Journal de Gynécologie Obstétrique et Biologie de la Reproduction. 39:168-171
Resume Une patiente primipare primigeste sans antecedent accouche spontanement a 40 semaines d’amenorrhee d’un enfant mort ne presentant un nœud serre au cordon ombilical. L’examen fœtopathologique confirme le role important mais non exclusif
Autor:
A. Azancot, Clarisse Baumann, A. L. Delezoide, E. Vuillard, Yvon Chitrit, K. R. M. Lopes, Dominique Luton
Publikováno v:
Prenatal Diagnosis. 26:696-699
Objectives Our objective was to describe the features of prenatal Marfan syndrome. Methods Doppler fetal echocardiograms were performed. The morphology and rhythm of the fetal heart were examined sequentially. Results The case was referred because of
Publikováno v:
Prenatal Diagnosis. 24:504-507
Congenital left ventricular diverticulum is a rare malformation. We report a case of a ruptured congenital left ventricular diverticulum in a 24-week-old fetus. The fetus was referred for a large and circumferential pericardial effusion confirmed by
Autor:
Fabien Guimiot, Jean-Michel Briffa, Margot Bucau, Emmanuel Spaggiari, Nadia Belarbi, Anais Bekmezian, Yline Capri, A. L. Delezoide
Publikováno v:
Prenatal Diagnosis. :1-3
Developmentally regulated expression of the murine ortholog of the potassium channel KIR4.2 (KCNJ15)
Autor:
A.-L Delezoide, Nicole Créau, Diane Damotte, N. de Saint-Sauveur, E. Thiery, Philippe Gosset, Catherine Vayssettes
Publikováno v:
Mechanisms of Development. 95:313-316
The gene KIR4.2 (K+ inwardly rectifying channel 4.2) has been recently identified in the Down syndrome Chromosome Region 1. We have cloned the mouse ortholog of KIR4.2 and characterized its expression pattern. In situ hybridization showed a restricte
Autor:
René Frydman, G. Chambon, Olivier Picone, M. V. Senat, A. L. Delezoide, A.-G. Cordier, M. Mabille
Publikováno v:
Prenatal Diagnosis. 28:975-977
We present the case of a 28-year-old woman, gravida1 para 0, who was referred at 22 weeks of gestation(WG) to our center to explore abnormalities revealedby second-trimester routine ultrasound examination. Thepatient’s medical and obstetrical histo
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Autor:
M.-Ch. Dauge-Geffroy, M.-Cl. Imbert, J.Cl. Larroche, N. Mulliez, D. Gaillard, A.-L. Delezoide
Publikováno v:
Revue Française des Laboratoires. 1998:33-39
Resume Les auteurs presentent ici les resultats d'une etude de cohorte, etude collaborative effectuee chez 313 grossesses gemellaires ou multiples, dans douze centres francais, entre 1988 et 1990. Ce travail a permis de decrire une grande partie de l