Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases
Adle-Biassette, Homa, Saugier-Veber, Pascale, Fallet-Bianco, Catherine, Delezoide, Anne-Lise, Razavi, Férecheté, Drouot, Nathalie, Bazin, Anne, Beaufrère, Anne-Marie, Bessières, Bettina, Blesson, Sophie, Bucourt, Martine, Carles, Dominique, Devisme, Louise, Dijoud, Frédérique, Fabre, Blandine, Fernandez, Carla, Gaillard, Dominique, Gonzales, Marie, Jossic, Frédérique, Joubert, Madeleine, Laurent, Nicole, Leroy, Brigitte, Loeuillet, Laurence, Loget, Philippe, Marcorelles, Pascale, Martinovic, Jelena, Perez, Marie-José, Satge, Daniel, Sinico, Martine, Tosi, Mario, Benichou, Jacques, Gressens, Pierre, Frebourg, Thierry, Laquerrière, Annie
Published in Acta neuropathologica (01.09.2013)
Published in Acta neuropathologica (01.09.2013)
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Minimal residual disease detection by multicolor flow cytometry in cryopreserved ovarian tissue from leukemia patients
Zver, Tristan, Frontczak, Sophie, Poirot, Catherine, Rives-Feraille, Aurélie, Leroy-Martin, Brigitte, Koscinski, Isabelle, Arbez-Gindre, Francine, Garnache-Ottou, Francine, Roux, Christophe, Amiot, Clotilde
Published in Journal of ovarian research (18.01.2022)
Published in Journal of ovarian research (18.01.2022)
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Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancy
Ben Miled, Selima, Loeuillet, Laurence, Duong Van Huyen, Jean-Paul, Bessières, Bettina, Sekour, Amel, Leroy, Brigitte, Tantau, Julia, Adle-Biassette, Homa, Salhi, Houria, Bonnière-Darcy, Maryse, Tessier, Aude, Martinovic, Jelena, Causeret, Frédéric, Bruneau, Julie, Saillour, Yoann, James, Syril, Ville, Yves, Attie-Bitach, Tania, Encha-Razavi, Ferechte, Stirnemann, Julien
Published in American journal of obstetrics and gynecology (01.08.2020)
Published in American journal of obstetrics and gynecology (01.08.2020)
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Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish
Reilly, Madeline Louise, Stokman, Marijn F, Magry, Virginie, Jeanpierre, Cecile, Alves, Marine, Paydar, Mohammadjavad, Hellinga, Jacqueline, Delous, Marion, Pouly, Daniel, Failler, Marion, Martinovic, Jelena, Loeuillet, Laurence, Leroy, Brigitte, Tantau, Julia, Roume, Joelle, Gregory-Evans, Cheryl Y, Shan, Xianghong, Filges, Isabel, Allingham, John S, Kwok, Benjamin H, Saunier, Sophie, Giles, Rachel H, Benmerah, Alexandre
Published in Human molecular genetics (01.03.2019)
Published in Human molecular genetics (01.03.2019)
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Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans
Humbert, Camille, Silbermann, Flora, Morar, Bharti, Parisot, Mélanie, Zarhrate, Mohammed, Masson, Cécile, Tores, Frédéric, Blanchet, Patricia, Perez, Marie-José, Petrov, Yuliya, Khau Van Kien, Philippe, Roume, Joelle, Leroy, Brigitte, Gribouval, Olivier, Kalaydjieva, Luba, Heidet, Laurence, Salomon, Rémi, Antignac, Corinne, Benmerah, Alexandre, Saunier, Sophie, Jeanpierre, Cécile
Published in American journal of human genetics (06.02.2014)
Published in American journal of human genetics (06.02.2014)
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Bardet‐Biedl syndrome: Antenatal presentation of forty‐five fetuses with biallelic pathogenic variants in known Bardet‐Biedl syndrome genes
Mary, Laura, Chennen, Kirsley, Stoetzel, Corinne, Antin, Manuela, Leuvrey, Anne, Nourisson, Elsa, Alanio‐Detton, Elisabeth, Antal, Maria C., Attié‐Bitach, Tania, Bouvagnet, Patrice, Bouvier, Raymonde, Buenerd, Annie, Clémenson, Alix, Devisme, Louise, Gasser, Bernard, Gilbert‐Dussardier, Brigitte, Guimiot, Fabien, Khau Van Kien, Philippe, Leroy, Brigitte, Loget, Philippe, Martinovic, Jelena, Pelluard, Fanny, Perez, Marie‐Josée, Petit, Florence, Pinson, Lucile, Rooryck‐Thambo, Caroline, Poch, Olivier, Dollfus, Hélène, Schaefer, Elise, Muller, Jean
Published in Clinical genetics (01.03.2019)
Published in Clinical genetics (01.03.2019)
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Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatment
Vinit, N., Bessières, B., Spaggiari, E., Heidet, L., Gubler, M.‐C., Dreux, S., Attie‐Bitach, T., Blanc, T., Ville, Y., Stirnemann, Julien J., Salomon, Laurent J., Loeuillet, Laurence, Bonnière, Maryse, Salhi, Houria, Roux, Nathalie, Petrilli, Giulia, Guimiot, Fabien, Khung‐Savatovsky, Suonavy, Rosenblatt, Jonathan, Quibel, Thibaud, Leroy, Brigitte, Tsatsaris, Vassilis, Anselem, Olivia, Grange, Gilles, Levaillant, Jean‐Marc, Talhi, Naima
Published in Ultrasound in obstetrics & gynecology (01.04.2022)
Published in Ultrasound in obstetrics & gynecology (01.04.2022)
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Fetal phenotype associated with the 22q11 deletion
Noël, Anne-Claire, Pelluard, Fanny, Delezoide, Anne-Lise, Devisme, Louise, Loeuillet, Laurence, Leroy, Brigitte, Martin, Alain, Bouvier, Raymonde, Laquerriere, Annie, Jeanne-Pasquier, Corinne, Bessieres-Grattagliano, Betty, Mechler, Charlotte, Alanio, Elisabeth, Leroy, Camille, Gaillard, Dominique
Published in American journal of medical genetics. Part A (01.11.2014)
Published in American journal of medical genetics. Part A (01.11.2014)
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Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations
Legendre, Marine, Gonzales, Marie, Goudefroye, Géraldine, Bilan, Frédéric, Parisot, Pauline, Perez, Marie-José, Bonnière, Maryse, Bessières, Bettina, Martinovic, Jelena, Delezoide, Anne-Lise, Jossic, Frédérique, Fallet-Bianco, Catherine, Bucourt, Martine, Tantau, Julia, Loget, Philippe, Loeuillet, Laurence, Laurent, Nicole, Leroy, Brigitte, Salhi, Houria, Bigi, Nicole, Rouleau, Caroline, Guimiot, Fabien, Quélin, Chloé, Bazin, Anne, Alby, Caroline, Ichkou, Amale, Gesny, Roselyne, Kitzis, Alain, Ville, Yves, Lyonnet, Stanislas, Razavi, Ferechte, Gilbert-Dussardier, Brigitte, Vekemans, Michel, Attié-Bitach, Tania
Published in Journal of medical genetics (01.11.2012)
Published in Journal of medical genetics (01.11.2012)
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Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies
Iannicelli, Miriam, Brancati, Francesco, Mougou-Zerelli, Soumaya, Mazzotta, Annalisa, Thomas, Sophie, Elkhartoufi, Nadia, Travaglini, Lorena, Gomes, Céline, Luigi Ardissino, Gian, Bertini, Enrico, Boltshauser, Eugen, Castorina, Pierangela, D'Arrigo, Stefano, Fischetto, Rita, Leroy, Brigitte, Loget, Philippe, Bonnière, Maryse, Starck, Lena, Tantau, Julia, Gentilin, Barbara, Majore, Silvia, Swistun, Dominika, Flori, Elizabeth, Lalatta, Faustina, Pantaleoni, Chiara, Penzien, Johannes, Grammatico, Paola, Dallapiccola, Bruno, Gleeson, Joseph G, Attie-Bitach, Tania, Valente, Enza Maria
Published in Human mutation (01.05.2010)
Published in Human mutation (01.05.2010)
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La question du tact en psychanalyse
Leroy-Viémon, Brigitte, Vives, Jean-Michel
Published in Psychothérapies (Geneva, Switzerland) (01.03.2015)
Published in Psychothérapies (Geneva, Switzerland) (01.03.2015)
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Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans
Humbert, Camille, Silbermann, Flora, Morar, Bharti, Parisot, Mélanie, Zarhrate, Mohammed, Masson, Cécile, Tores, Frédéric, Blanchet, Patricia, Perez, Marie-José, Petrov, Yuliya, Khau Van Kien, Philippe, Roume, Joelle, Leroy, Brigitte, Gribouval, Olivier, Kalaydjieva, Luba, Heidet, Laurence, Salomon, Rémi, Antignac, Corinne, Benmerah, Alexandre, Saunier, Sophie, Jeanpierre, Cécile
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
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Prospective assessment of follicular growth and the oocyte cohort after ovarian stimulation for fertility preservation in 90 cancer patients versus 180 matched controls
Decanter, Christine, Robin, Geoffroy, Mailliez, Audrey, Sigala, Julien, Morschhauser, Franck, Ramdane, Nassima, Devos, Patrick, Dewailly, Didier, Leroy-Martin, Brigitte, Keller, Laura
Published in Reproductive biomedicine online (01.05.2018)
Published in Reproductive biomedicine online (01.05.2018)
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Prenatal diagnosis of de novo (7;19)(q11.2;q13.3) translocation associated with a thick corpus callosum and Wilms tumor of the kidneys
Cavicchioni, Ottavia, Gomes, Denise Molina, Leroy, Brigitte, Vialard, François, Hillion, Yvette, Selva, Jacqueline, Ville, Yves
Published in Prenatal diagnosis (01.10.2005)
Published in Prenatal diagnosis (01.10.2005)
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Comparison of four fluorochromes for the detection of the inner mitochondrial membrane potential in human spermatozoa and their correlation with sperm motility
Marchetti, Carole, Jouy, Nathalie, Leroy-Martin, Brigitte, Defossez, André, Formstecher, Pierre, Marchetti, Philippe
Published in Human reproduction (Oxford) (01.10.2004)
Published in Human reproduction (Oxford) (01.10.2004)
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