Zobrazeno 1 - 10
of 116
pro vyhledávání: '"V Kerbrat"'
Autor:
Nadine Gigarel, Frédéric Lamazou, V. Kerbrat, Philippe Burlet, Josué Feingold, David C. Samuels, Laetitia Hesters, Agnès Rötig, Nelly Frydman, Arnold Munnich, Julie Steffann, Sophie Monnot, René Frydman, Alexandra Benachi, Jean-Paul Bonnefont
Publikováno v:
Human Molecular Genetics. 22:1867-1872
Mitochondrial DNA (mtDNA) content is thought to remain stable over the preimplantation period of human embryogenesis that is, therefore, suggested to be entirely dependent on ooplasm mtDNA capital. We have explored the impact of two disease-causing m
Diagnostic préimplantatoire avec typage HLA : naissance du premier enfant du double espoir en France
Autor:
Michel Vekemans, JP Bonnefont, Philippe Burlet, V. Kerbrat, S. Romana, Laetitia Hesters, René Frydman, N. Frydman, M. Lelorc’h, Nadine Gigarel, Arnold Munnich, Julie Steffann, R. Fanchin, F. Lamazou
Publikováno v:
Journal de Gynécologie Obstétrique et Biologie de la Reproduction. 40:682-686
Journal de Gynecologie Obstetrique et Biologie de la Reproduction - Vol. 40 - N° 7 - p. 682-686
Autor:
Philippe Burlet, Laetitia Hesters, Nelly Frydman, René Frydman, Nadine Gigarel, Arnold Munnich, Julie Steffann, V. Kerbrat, F. Lamazou
Publikováno v:
Bulletin de l'Académie Nationale de Médecine. 195:1015-1022
Umut-Talha, a "sibling savior", was born on 26 January 2011 at Beclere Hospital after embryo selection at the Paris preimplantation genetic diagnosis (PGD) center. His birth revived the controversy over "double PGD". This procedure, authorized in Fra
Autor:
Alexandra Benachi, F. Lamazou, David C. Samuels, Nadine Gigarel, Sophie Monnot, Agnès Rötig, V. Kerbrat, Arnold Munnich, Jean-Paul Bonnefont, René Frydman, Philippe Burlet, Nelly Frydman, Julie Steffann, Laetitia Hesters, Josué Feingold
Publikováno v:
The American Journal of Human Genetics. 88:494-498
Because the mtDNA amount remains stable in the early embryo until uterine implantation, early human development is completely dependent on the mtDNA pool of the mature oocyte. Both quantitative and qualitative mtDNA defects therefore may negatively i
Autor:
Arnold Munnich, F. Lamazou, Marc Le Lorc’h, Julie Steffann, Serge Romana, Jean-Paul Bonnefont, Renato Fanchin, Nadine Gigarel, V. Kerbrat, Michel Vekemans, Laetitia Hesters, René Frydman, Nelly Achour-Frydman, Philippe Burlet
Publikováno v:
Bulletin de l'Académie Nationale de Médecine. 195:1005-1014
Preimplantation genetic diagnosis (PGD) has been authorized in France since 1999. Encouraging results have been obtained during the past 10 years in our Paris center, where 832 patients have undergone 1056 IVF-PGD procedures. With the advent of new t
Autor:
G Tachdjian, Philippe Burlet, René Frydman, Nadine Gigarel, Corinne Antignac, V. Kerbrat, Renato Fanchin, Arnold Munnich, Nelly Frydman, Julie Steffann
Publikováno v:
Scopus-Elsevier
Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary renal cystic diseases, and is caused by mutations in the PKHD1 gene. Due to the poor prognosis, there is a strong demand for prenatal diagnosis. Preimplantatio
Autor:
Philippe Burlet, E. Feyereisen, Arnold Munnich, René Frydman, Nadine Gigarel, V. Kerbrat, Jean-Paul Bonnefont, Gérard Tachdjian, Julie Steffann, Nelly Frydman
Publikováno v:
MHR: Basic science of reproductive medicine. 12:647-652
We report an improvement in the PGD test for fragile X syndrome (FXS). Recently, multiple displacement amplification (MDA) has been reported to yield large amounts of DNA from single cells. Taking into account this technique, we developed a new PGD t
Autor:
René Frydman, E. Feyereisen, Michel Vekemans, R. Fanchin, Arnold Munnich, S. Romana, Nelly Frydman, Nadine Gigarel, L Foix-L’Hélias, G Tachdjian, V. Kerbrat, M. Lelorc’h, S. Hamamah, Nicolas Chevalier, Philippe Burlet, Pierre F. Ray, Julie Steffann
Publikováno v:
Journal de Gynécologie Obstétrique et Biologie de la Reproduction. 35:356-372
Journal de Gynecologie Obstetrique et Biologie de la Reproduction - Vol. 35 - N° 4 - p. 356-372
Autor:
Nelly Frydman, E. Feyereisen, René Frydman, Nadine Gigarel, G Tachdjian, V. Kerbrat, Arnold Munnich, Julie Steffann, Philippe Burlet
Publikováno v:
Gynécologie Obstétrique & Fertilité. 33:824-827
Resume Le diagnostic preimplantatoire (DPI) repose sur l'analyse genetique de une a deux cellules embryonnaires (blastomeres), prelevees sur des embryons obtenus par fecondation in vitro au troisieme jour de leur developpement. Encadre par un arsenal
Publikováno v:
Gynécologie Obstétrique & Fertilité. 33:235-238
Resume Objectif. – Comprendre les motifs psychiques qui ont amene les couples a prendre le risque de transmission genetique et a envisager une nouvelle grossesse spontanee. Tenter d'expliquer pourquoi lors d'une demande de diagnostic genetique prei