Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Nelly Frydman"'
Autor:
Manon Carles, Charlotte Sonigo, Olivier Binois, Laetitia Hesters, Julie Steffann, Serge Romana, Nelly Frydman, Anne Mayeur
Publikováno v:
Journal of gynecology obstetrics and human reproduction. 51(8)
In this study, we aimed to evaluate the pregnancy outcomes for embryos biopsied twice at cleavage and blastocyst stage for preimplantation genetic testing (PGT). This retrospective monocentric study, conducted between January 2016 and March 2021, des
Autor:
Jade Raad, Sophie Monnot, Laetitia Hesters, Nelly Frydman, Anne Mayeur, Julie Steffann, Alexandre Levy, Vincent Puy
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:1137-1144
Context Myotonic dystrophy (DM) is an autosomal dominant disorder characterized mainly by myotonia but also by primary hypogonadism. No study has reported on fertility management of patients affected by DM type 1 (DM1). Objective This study investiga
Autor:
Serge Romana, Laetitia Hesters, Michael Grynberg, Nelly Frydman, Charlotte Sonigo, Naouel Ahdad, Anne Mayeur
Publikováno v:
Reproductive BioMedicine
Reproductive BioMedicine Online, Elsevier, 2020, 40, pp.684-692. ⟨10.1016/j.rbmo.2020.01.025⟩
Reproductive BioMedicine Online, 2020, 40, pp.684-692. ⟨10.1016/j.rbmo.2020.01.025⟩
Reproductive BioMedicine Online, Elsevier, 2020, 40, pp.684-692. ⟨10.1016/j.rbmo.2020.01.025⟩
Reproductive BioMedicine Online, 2020, 40, pp.684-692. ⟨10.1016/j.rbmo.2020.01.025⟩
Research question Chromosomal translocations are known genetic causes of premature ovarian insufficiency syndrome. Are certain translocations associated with decreased capacity of small antral follicles to respond to exogenous FSH? Does the prognosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fc6d288078f8416bf64a0bc4f648e2f
https://hal.archives-ouvertes.fr/hal-03490933
https://hal.archives-ouvertes.fr/hal-03490933
Publikováno v:
Cell Stem Cell. 22:481-482
Autor:
Nelly, Frydman
Publikováno v:
Medecine sciences : M/S. 32(2)
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:
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:
Nadine Gigarel, Nelly Frydman, V. Kerbrat, Pierre F. Ray, Arnold Munnich, René Frydman, Philippe Burlet, Julie Steffann
Publikováno v:
Human Genetics. 114:298-305
Preimplantation genetic diagnosis (PGD) first consisted of the selection of female embryos for patients at risk of transmitting X-linked recessive diseases. Advances in molecular biology now allow the specific diagnosis of almost any Mendelian diseas
Publikováno v:
Journal of Assisted Reproduction and Genetics. 21:7-9
In vitro fertilization is strongly regulated in France. An agreement is needed for the clinicians and the embryologists; and the activity is under the control of CNMBRDP, a governmental commission. PGD is even more controlled; an agreement is needed