Torthaí cuardaigh - Koscinski, Isabelle
- 1 - 12 toradh as 12 á dtaispeáint
-
1
Hypogonadotropic hypogonadism in men with hereditary hemochromatosis de réir El Osta, Rabih, Grandpre, Nicolas, Monnin, Nicolas, Hubert, Jacques, Koscinski, Isabelle
Foilsithe / Cruthaithe 2017Téacs -
2
Ovarian Telomerase and Female Fertility de réir Toupance, Simon, Fattet, Anne-Julie, Thornton, Simon N., Benetos, Athanase, Guéant, Jean-Louis, Koscinski, Isabelle
Foilsithe / Cruthaithe 2021Téacs -
3
Telomere length in granulosa cells and leukocytes: a potential marker of female fertility? A systematic review of the literature de réir Fattet, Anne-Julie, Toupance, Simon, Thornton, Simon N., Monnin, Nicolas, Guéant, Jean-Louis, Benetos, Athanase, Koscinski, Isabelle
Foilsithe / Cruthaithe 2020Téacs -
4
Reproduction Function in Male Patients With Bardet Biedl Syndrome de réir Koscinski, Isabelle, Mark, Manuel, Messaddeq, Nadia, Braun, Jean Jacques, Celebi, Catherine, Muller, Jean, Zinetti-Bertschy, Anna, Goetz, Nathalie, Dollfus, Hélène, Rossignol, Sylvie
Foilsithe / Cruthaithe 2020Téacs -
5
Minimal residual disease detection by multicolor flow cytometry in cryopreserved ovarian tissue from leukemia patients de réir Zver, Tristan, Frontczak, Sophie, Poirot, Catherine, Rives-Feraille, Aurélie, Leroy-Martin, Brigitte, Koscinski, Isabelle, Arbez-Gindre, Francine, Garnache-Ottou, Francine, Roux, Christophe, Amiot, Clotilde
Foilsithe / Cruthaithe 2022Téacs -
6
Multiorgan and Vascular Tropism of SARS-CoV-2 de réir Hartard, Cédric, Chaqroun, Ahlam, Settembre, Nicla, Gauchotte, Guillaume, Lefevre, Benjamin, Marchand, Elodie, Mazeaud, Charles, Nguyen, Duc Trung, Martrille, Laurent, Koscinski, Isabelle, Malikov, Sergueï, Schvoerer, Evelyne
Foilsithe / Cruthaithe 2022Téacs -
7
Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia de réir Dam, Anika H. D. M. , Koscinski, Isabelle , Kremer, Jan A. M. , Moutou, Céline , Jaeger, Anne-Sophie , Oudakker, Astrid R. , Tournaye, Herman , Charlet, Nicolas , Lagier-Tourenne, Clotilde , van Bokhoven, Hans , Viville, Stéphane
Foilsithe / Cruthaithe 2007Téacs -
8
DPY19L2 Deletion as a Major Cause of Globozoospermia de réir Koscinski, Isabelle, ElInati, Elias, Fossard, Camille, Redin, Claire, Muller, Jean, Velez de la Calle, Juan, Schmitt, Françoise, Ben Khelifa, Mariem, Ray, Pierre, Kilani, Zaid, Barratt, Christopher L.R., Viville, Stéphane
Foilsithe / Cruthaithe 2011Téacs -
9
DPY19L2 Deletion as a Major Cause of Globozoospermia de réir Koscinski, Isabelle, ElInati, Elias, Fossard, Camille, Redin, Claire, Muller, Jean, Velez de la Calle, Juan, Schmitt, Françoise, Ben Khelifa, Mariem, Ray, Pierre F., Kilani, Zaid, Barratt, Christopher L.R., Viville, Stéphane
Foilsithe / Cruthaithe 2011Téacs -
10
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation de réir Harbuz, Radu, Zouari, Raoudha, Pierre, Virginie, Ben Khelifa, Mariem, Kharouf, Mahmoud, Coutton, Charles, Merdassi, Ghaya, Abada, Farid, Escoffier, Jessica, Nikas, Yorgos, Vialard, François, Koscinski, Isabelle, Triki, Chema, Sermondade, Nathalie, Schweitzer, Thérèse, Zhioua, Amel, Zhioua, Fethi, Latrous, Habib, Halouani, Lazhar, Ouafi, Marrakchi, Makni, Mounir, Jouk, Pierre-Simon, Sèle, Bernard, Hennebicq, Sylviane, Satre, Véronique, Viville, Stéphane, Arnoult, Christophe, Lunardi, Joël, Ray, Pierre F.
Foilsithe / Cruthaithe 2011Téacs -
11
A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients de réir Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.
Foilsithe / Cruthaithe 2018Téacs -
12
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients de réir Guéant, Jean-Louis, Chéry, Céline, Oussalah, Abderrahim, Nadaf, Javad, Coelho, David, Josse, Thomas, Flayac, Justine, Robert, Aurélie, Koscinski, Isabelle, Gastin, Isabelle, Filhine-Tresarrieu, Pierre, Pupavac, Mihaela, Brebner, Alison, Watkins, David, Pastinen, Tomi, Montpetit, Alexandre, Hariri, Fadi, Tregouët, David, Raby, Benjamin A, Chung, Wendy K., Morange, Pierre-Emmanuel, Froese, D. Sean, Baumgartner, Matthias R., Benoist, Jean-François, Ficicioglu, Can, Marchand, Virginie, Motorin, Yuri, Bonnemains, Chrystèle, Feillet, François, Majewski, Jacek, Rosenblatt, David S.
Foilsithe / Cruthaithe 2018Téacs