NR5A1 ( SF-1 ) gene variants in a group of 26 young women with XX primary ovarian insufficiency von Philibert, Pascal, Pharm.D., Ph.D, Paris, Françoise, M.D., Ph.D, Lakhal, Besma, Ph.D, Audran, Françoise, Pharm.D, Gaspari, Laura, M.D, Saâd, Ali, M.D., Ph.D, Christin-Maître, Sophie, M.D., Ph.D, Bouchard, Philippe, M.D., Ph.D, Sultan, Charles, M.D., Ph.D

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Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans von Laissue, Paul, Lakhal, Besma, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Gris, Jean-Christophe, Cocquet, Julie, Vaiman, Daniel

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A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure von Lakhal, Besma, Laissue, Paul, Braham, Rim, Elghezal, Hatem, Saâd, Ali, Fellous, Marc, Veitia, Reiner A.

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Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype von Ojeda, Diego, M.Sc, Lakhal, Besma, Ph.D, Fonseca, Dora Janneth, M.Sc, Braham, Rim, M.D, Landolsi, Hanène, Ph.D, Mateus, Heidi Eliana, M.D, Restrepo, Carlos Martín, M.D., Ph.D, Elghezal, Hatem, M.D, Saâd, Ali, M.D., Ph.D, Laissue, Paul, M.D., Ph.D

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Corrigendum to “Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure” [Gene 509 (2012) 298–301] von Lakhal, Besma, Ben-Hadj-Khalifa, Sonia, Bouali, Nouha, Braham, Rim, Hatem, Elghezal, Saad, Ali

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Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure von Lakhal, Besma, Ben-Hadj-Khalifa, Sonia, Bouali, Nouha, Philipert, Pascal, Audran, Françoise, Braham, Rim, Hatem, Elghezal, Sultan, Charles, Saad, Ali

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Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2 von Laissue, P, Lakhal, B, Benayoun, B A, Dipietromaria, A, Braham, R, Elghezal, H, Philibert, P, Saâd, A, Sultan, C, Fellous, M, Veitia, R A

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BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms? von Lakhal, Besma, Laissue, Paul, Braham, Rim, Elghezal, Hatem, Saâd, Ali, Fellous, Marc, Veitia, Reiner A.

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Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure von Bouali, Nouha, Hmida, Dorra, Mougou, Soumaya, Bouligand, Jérôme, Lakhal, Besma, Dimessi, Sarra, Francou, Bruno, Saad, Ghada, Trabelsi, Saoussen, Zaouali, Monia, Gribaa, Moez, Chaieb, Molka, Bibi, Mouhamed, Guiochon-Mantel, Anne, Saad, Ali

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CITED2 mutations potentially cause idiopathic premature ovarian failure von Fonseca, Dora Janeth, Ojeda, Diego, Lakhal, Besma, Braham, Rim, Eggers, Stefanie, Turbitt, Erin, White, Stefan, Grover, Sonia, Warne, Garry, Zacharin, Margaret, Nevin Lam, Alexandra, Landolsi, Hanène, Elghezal, Hatem, Saâd, Ali, Restrepo, Carlos Martín, Fellous, Marc, Sinclair, Andrew, Koopman, Peter, Laissue, Paul

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Screening for mutations of the FOXO4 gene in premature ovarian failure patients von Fonseca, Dora Janeth, Garzón, Eliana, Lakhal, Besma, Braham, Rim, Ojeda, Diego, Elghezal, Hatem, Saâd, Ali, Restrepo, Carlos Martín, Laissue, Paul

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Table S1 from Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans von Laissue, Paul, Besma Lakhal, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Jean-Christophe Gris, Cocquet, Julie, Vaiman, Daniel

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Figure S1 from Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans von Laissue, Paul, Besma Lakhal, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Jean-Christophe Gris, Cocquet, Julie, Vaiman, Daniel

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Table S3 from Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans von Laissue, Paul, Besma Lakhal, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Jean-Christophe Gris, Cocquet, Julie, Vaiman, Daniel

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Table S2 from Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans von Laissue, Paul, Besma Lakhal, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Jean-Christophe Gris, Cocquet, Julie, Vaiman, Daniel

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A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure von Lakhal, Besma, Laissue, Paul, Braham, Rim, Elghezal, Hatem, Saâd, Ali, Fellous, Marc, Veitia, Reiner A

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Serious bullous cutaneous lesions induced by isoniazid von Trabelsi, Sameh, El Aïdli, Sihem, Amrani, Radhia, Ourari, Besma, Klouz, Anis, Lakhal, Mohamed, Loueslati, Mohamed Hédi, Daghfous, Riadh, Beji, Majed, Belkahia, Chalbi

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Lésions cutanées bulleuses graves induites par l’isoniazide von Trabelsi, Sameh, El Aïdli, Sihem, Amrani, Radhia, Ourari, Besma, Klouz, Anis, Lakhal, Mohamed, Loueslati, Mohamed Hédi, Daghfous, Riadh, Beji, Majed, Belkahia, Chalbi

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