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<title>Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/78809" rel="alternate"/>
<subtitle/>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/78809</id>
<updated>2026-04-06T09:24:53Z</updated>
<dc:date>2026-04-06T09:24:53Z</dc:date>
<entry>
<title>Case report: Two siblings with very late onset of holocarboxylase synthase deficiency and a mini-review</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/207331" rel="alternate"/>
<author>
<name>GASCHIGNARD, Margaux</name>
</author>
<author>
<name>DOMENACH, Louis</name>
</author>
<author>
<name>LAMIREAU, Delphine</name>
</author>
<author>
<name>GUIBET, Claire</name>
</author>
<author>
<name>ROCHE, Sandrine</name>
</author>
<author>
<name>RICHARD, Emmanuel</name>
</author>
<author>
<name>REDONNET VERNHET, Isabelle</name>
</author>
<author>
<name>MESLI, Samir</name>
</author>
<author>
<name>LEBRETON, Louis</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/207331</id>
<updated>2025-07-15T12:36:35Z</updated>
<published>2024-09-26T00:00:00Z</published>
<summary type="text">GASCHIGNARD, Margaux; DOMENACH, Louis; LAMIREAU, Delphine; GUIBET, Claire; ROCHE, Sandrine; RICHARD, Emmanuel; REDONNET VERNHET, Isabelle; MESLI, Samir; LEBRETON, Louis
</summary>
<dc:date>2024-09-26T00:00:00Z</dc:date>
</entry>
<entry>
<title>Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/207330" rel="alternate"/>
<author>
<name>DEMIDOV, German</name>
</author>
<author>
<name>LAURIE, Steven</name>
</author>
<author>
<name>TORELLA, Annalaura</name>
</author>
<author>
<name>PILUSO, Giulio</name>
</author>
<author>
<name>SCALA, Marcello</name>
</author>
<author>
<name>MORLEO, Manuela</name>
</author>
<author>
<name>NIGRO, Vincenzo</name>
</author>
<author>
<name>GRAESSNER, Holm</name>
</author>
<author>
<name>BANKA, Siddharth</name>
</author>
<author>
<name>MACAYA, Alfons</name>
</author>
<author>
<name>PÉREZ-DUEÑAS, Belén</name>
</author>
<author>
<name>JACKSON, Adam</name>
</author>
<author>
<name>STEVANIN, Giovanni</name>
</author>
<author>
<name>DE SAINTE AGATHE, Jean-Madeleine</name>
</author>
<author>
<name>HAVLOVICOVÁ, Markéta</name>
</author>
<author>
<name>HORVATH, Rita</name>
</author>
<author>
<name>PINELLI, Michele</name>
</author>
<author>
<name>VAN OS, Nienke J. H.</name>
</author>
<author>
<name>VAN DE WARRENBURG, Bart P. C.</name>
</author>
<author>
<name>DENOMMÉ-PICHON, Anne-Sophie</name>
</author>
<author>
<name>SAVARESE, Marco</name>
</author>
<author>
<name>JOHARI, Mridul</name>
</author>
<author>
<name>DALLAPICCOLA, Bruno</name>
</author>
<author>
<name>TARTAGLIA, Marco</name>
</author>
<author>
<name>PAULY, Martje G.</name>
</author>
<author>
<name>SOMMER, Anna Katharina</name>
</author>
<author>
<name>HAACK, Tobias B.</name>
</author>
<author>
<name>TÖPF, Ana</name>
</author>
<author>
<name>DIDIER, Lacombe</name>
</author>
<author>
<name>FALLERINI, Chiara</name>
</author>
<author>
<name>RENIERI, Alessandra</name>
</author>
<author>
<name>CHINNERY, Patrick F.</name>
</author>
<author>
<name>NATERA-DE BENITO, Daniel</name>
</author>
<author>
<name>NASCIMENTO, Andres</name>
</author>
<author>
<name>TRIMOUILLE, Aurélien</name>
</author>
<author>
<name>MUNELL, Francina</name>
</author>
<author>
<name>MARCÉ-GRAU, Anna</name>
</author>
<author>
<name>RABAH, Ben Yaou</name>
</author>
<author>
<name>BONNE, Gisèle</name>
</author>
<author>
<name>VAN DE VONDEL, Liedewei</name>
</author>
<author>
<name>LOHMANN, Katja</name>
</author>
<author>
<name>OSSOWSKI, Stephan</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/207330</id>
<updated>2025-07-15T11:47:56Z</updated>
<published>2024-08-01T00:00:00Z</published>
<summary type="text">DEMIDOV, German; LAURIE, Steven; TORELLA, Annalaura; PILUSO, Giulio; SCALA, Marcello; MORLEO, Manuela; NIGRO, Vincenzo; GRAESSNER, Holm; BANKA, Siddharth; MACAYA, Alfons; PÉREZ-DUEÑAS, Belén; JACKSON, Adam; STEVANIN, Giovanni; DE SAINTE AGATHE, Jean-Madeleine; HAVLOVICOVÁ, Markéta; HORVATH, Rita; PINELLI, Michele; VAN OS, Nienke J. H.; VAN DE WARRENBURG, Bart P. C.; DENOMMÉ-PICHON, Anne-Sophie; SAVARESE, Marco; JOHARI, Mridul; DALLAPICCOLA, Bruno; TARTAGLIA, Marco; PAULY, Martje G.; SOMMER, Anna Katharina; HAACK, Tobias B.; TÖPF, Ana; DIDIER, Lacombe; FALLERINI, Chiara; RENIERI, Alessandra; CHINNERY, Patrick F.; NATERA-DE BENITO, Daniel; NASCIMENTO, Andres; TRIMOUILLE, Aurélien; MUNELL, Francina; MARCÉ-GRAU, Anna; RABAH, Ben Yaou; BONNE, Gisèle; VAN DE VONDEL, Liedewei; LOHMANN, Katja; OSSOWSKI, Stephan
</summary>
<dc:date>2024-08-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Transcriptome and acetylome profiling identify crucial steps of neuronal differentiation in Rubinstein-Taybi syndrome</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/207329" rel="alternate"/>
<author>
<name>VAN-GILS, Julien</name>
</author>
<author>
<name>KARKAR, Slim</name>
</author>
<author>
<name>BARRE, Aurelien</name>
</author>
<author>
<name>LEY-NGARDIGAL, Seyta</name>
</author>
<author>
<name>NOTHOF, Sophie</name>
</author>
<author>
<name>CLAVEROL, Stephane</name>
</author>
<author>
<name>TOKARSKI, Caroline</name>
</author>
<author>
<name>TRANI, Jean-Philippe</name>
</author>
<author>
<name>CHEVALIER, Raphael</name>
</author>
<author>
<name>BROUCQSAULT, Natacha</name>
</author>
<author>
<name>EL YAZIDI, Claire</name>
</author>
<author>
<name>LACOMBE, Didier</name>
</author>
<author>
<name>FERGELOT, Patricia</name>
</author>
<author>
<name>MAGDINIER, Frédérique</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/207329</id>
<updated>2025-07-15T11:28:18Z</updated>
<published>2024-10-15T00:00:00Z</published>
<summary type="text">VAN-GILS, Julien; KARKAR, Slim; BARRE, Aurelien; LEY-NGARDIGAL, Seyta; NOTHOF, Sophie; CLAVEROL, Stephane; TOKARSKI, Caroline; TRANI, Jean-Philippe; CHEVALIER, Raphael; BROUCQSAULT, Natacha; EL YAZIDI, Claire; LACOMBE, Didier; FERGELOT, Patricia; MAGDINIER, Frédérique
</summary>
<dc:date>2024-10-15T00:00:00Z</dc:date>
</entry>
<entry>
<title>Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/207328" rel="alternate"/>
<author>
<name>BARISH, Scott</name>
</author>
<author>
<name>LIN, Sheng-Jia</name>
</author>
<author>
<name>MAROOFIAN, Reza</name>
</author>
<author>
<name>GEZDIRICI, Alper</name>
</author>
<author>
<name>ALHEBBY, Hamoud</name>
</author>
<author>
<name>TRIMOUILLE, Aurelien</name>
</author>
<author>
<name>WABERSKI, Marta Biderman</name>
</author>
<author>
<name>MITANI, Tadahiro</name>
</author>
<author>
<name>HUBER, Ilka</name>
</author>
<author>
<name>TVETEN, Kristian</name>
</author>
<author>
<name>HOLLA, Øystein L.</name>
</author>
<author>
<name>BUSK, Øyvind L.</name>
</author>
<author>
<name>HOULDEN, Henry</name>
</author>
<author>
<name>KARIMIANI, Ehsan Ghayoor</name>
</author>
<author>
<name>TOOSI, Mehran Beiraghi</name>
</author>
<author>
<name>BADV, Reza Shervin</name>
</author>
<author>
<name>TORBATI, Paria Najarzadeh</name>
</author>
<author>
<name>EGHBAL, Fatemeh</name>
</author>
<author>
<name>AKHONDIAN, Javad</name>
</author>
<author>
<name>AL SAFAR, Ayat</name>
</author>
<author>
<name>ALSWAID, Abdulrahman</name>
</author>
<author>
<name>ZIFARELLI, Giovanni</name>
</author>
<author>
<name>BAUER, Peter</name>
</author>
<author>
<name>MARAFI, Dana</name>
</author>
<author>
<name>FATIH, Jawid M.</name>
</author>
<author>
<name>HUANG, Kevin</name>
</author>
<author>
<name>PETREE, Cassidy</name>
</author>
<author>
<name>CALAME, Daniel G.</name>
</author>
<author>
<name>VON DER LIPPE, Charlotte</name>
</author>
<author>
<name>ALKURAYA, Fowzan S.</name>
</author>
<author>
<name>WALI, Sami</name>
</author>
<author>
<name>LUPSKI, James R.</name>
</author>
<author>
<name>VARSHNEY, Gaurav K.</name>
</author>
<author>
<name>POSEY, Jennifer E.</name>
</author>
<author>
<name>PEHLIVAN, Davut</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/207328</id>
<updated>2025-07-15T10:03:53Z</updated>
<published>2024-11-07T00:00:00Z</published>
<summary type="text">BARISH, Scott; LIN, Sheng-Jia; MAROOFIAN, Reza; GEZDIRICI, Alper; ALHEBBY, Hamoud; TRIMOUILLE, Aurelien; WABERSKI, Marta Biderman; MITANI, Tadahiro; HUBER, Ilka; TVETEN, Kristian; HOLLA, Øystein L.; BUSK, Øyvind L.; HOULDEN, Henry; KARIMIANI, Ehsan Ghayoor; TOOSI, Mehran Beiraghi; BADV, Reza Shervin; TORBATI, Paria Najarzadeh; EGHBAL, Fatemeh; AKHONDIAN, Javad; AL SAFAR, Ayat; ALSWAID, Abdulrahman; ZIFARELLI, Giovanni; BAUER, Peter; MARAFI, Dana; FATIH, Jawid M.; HUANG, Kevin; PETREE, Cassidy; CALAME, Daniel G.; VON DER LIPPE, Charlotte; ALKURAYA, Fowzan S.; WALI, Sami; LUPSKI, James R.; VARSHNEY, Gaurav K.; POSEY, Jennifer E.; PEHLIVAN, Davut
</summary>
<dc:date>2024-11-07T00:00:00Z</dc:date>
</entry>
<entry>
<title>Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/206781" rel="alternate"/>
<author>
<name>LAURIE, Steven</name>
</author>
<author>
<name>STEYAERT, Wouter</name>
</author>
<author>
<name>DE BOER, Elke</name>
</author>
<author>
<name>POLAVARAPU, Kiran</name>
</author>
<author>
<name>SCHUERMANS, Nika</name>
</author>
<author>
<name>SOMMER, Anna K</name>
</author>
<author>
<name>DEMIDOV, German</name>
</author>
<author>
<name>ELLWANGER, Kornelia</name>
</author>
<author>
<name>PARAMONOV, Ida</name>
</author>
<author>
<name>THOMAS, Coline</name>
</author>
<author>
<name>ARETZ, Stefan</name>
</author>
<author>
<name>BAETS, Jonathan</name>
</author>
<author>
<name>BENETTI, Elisa</name>
</author>
<author>
<name>BULLICH, Gemma</name>
</author>
<author>
<name>CHINNERY, Patrick F</name>
</author>
<author>
<name>CLAYTON-SMITH, Jill</name>
</author>
<author>
<name>COHEN, Enzo</name>
</author>
<author>
<name>DANIS, Daniel</name>
</author>
<author>
<name>DE SAINTE AGATHE, Jean-Madeleine</name>
</author>
<author>
<name>DENOMMÉ-PICHON, Anne-Sophie</name>
</author>
<author>
<name>DIAZ-MANERA, Jordi</name>
</author>
<author>
<name>EFTHYMIOU, Stephanie</name>
</author>
<author>
<name>FAIVRE, Laurence</name>
</author>
<author>
<name>FERNANDEZ-CALLEJO, Marcos</name>
</author>
<author>
<name>FREEBERG, Mallory</name>
</author>
<author>
<name>GARCIA-PELAEZ, José</name>
</author>
<author>
<name>GUILLOT-NOEL, Lena</name>
</author>
<author>
<name>HAACK, Tobias B</name>
</author>
<author>
<name>HANNA, Mike</name>
</author>
<author>
<name>HENGEL, Holger</name>
</author>
<author>
<name>HORVATH, Rita</name>
</author>
<author>
<name>HOULDEN, Henry</name>
</author>
<author>
<name>JACKSON, Adam</name>
</author>
<author>
<name>JOHANSSON, Lennart</name>
</author>
<author>
<name>JOHARI, Mridul</name>
</author>
<author>
<name>KAMSTEEG, Erik-Jan</name>
</author>
<author>
<name>KELLNER, Melanie</name>
</author>
<author>
<name>KLEEFSTRA, Tjitske</name>
</author>
<author>
<name>LACOMBE, Didier</name>
</author>
<author>
<name>LOCHMÜLLER, Hanns</name>
</author>
<author>
<name>LÓPEZ-MARTÍN, Estrella</name>
</author>
<author>
<name>MACAYA, Alfons</name>
</author>
<author>
<name>MARCÉ-GRAU, Anna</name>
</author>
<author>
<name>MAVER, Aleš</name>
</author>
<author>
<name>MORSY, Heba</name>
</author>
<author>
<name>MUNTONI, Francesco</name>
</author>
<author>
<name>MUSACCHIA, Francesco</name>
</author>
<author>
<name>NELSON, Isabelle</name>
</author>
<author>
<name>NIGRO, Vincenzo</name>
</author>
<author>
<name>OLIMPIO, Catarina</name>
</author>
<author>
<name>OLIVEIRA, Carla</name>
</author>
<author>
<name>PAULASOVÁ SCHWABOVÁ, Jaroslava</name>
</author>
<author>
<name>PAULY, Martje G</name>
</author>
<author>
<name>PETERLIN, Borut</name>
</author>
<author>
<name>PETERS, Sophia</name>
</author>
<author>
<name>PFUNDT, Rolph</name>
</author>
<author>
<name>PILUSO, Giulio</name>
</author>
<author>
<name>PISCIA, Davide</name>
</author>
<author>
<name>POSADA, Manuel</name>
</author>
<author>
<name>REICH, Selina</name>
</author>
<author>
<name>RENIERI, Alessandra</name>
</author>
<author>
<name>RYBA, Lukas</name>
</author>
<author>
<name>ŠABLAUSKAS, Karolis</name>
</author>
<author>
<name>SAVARESE, Marco</name>
</author>
<author>
<name>SCHÖLS, Ludger</name>
</author>
<author>
<name>SCHÜTZ, Leon</name>
</author>
<author>
<name>STEINKE-LANGE, Verena</name>
</author>
<author>
<name>STEVANIN, Giovanni</name>
</author>
<author>
<name>STRAUB, Volker</name>
</author>
<author>
<name>STURM, Marc</name>
</author>
<author>
<name>SWERTZ, Morris A</name>
</author>
<author>
<name>TARTAGLIA, Marco</name>
</author>
<author>
<name>TE PASKE, Iris B A W</name>
</author>
<author>
<name>THOMPSON, Rachel</name>
</author>
<author>
<name>TORELLA, Annalaura</name>
</author>
<author>
<name>TRAINOR, Christina</name>
</author>
<author>
<name>UDD, Bjarne</name>
</author>
<author>
<name>VAN DE VONDEL, Liedewei</name>
</author>
<author>
<name>VAN DE WARRENBURG, Bart</name>
</author>
<author>
<name>VAN REEUWIJK, Jeroen</name>
</author>
<author>
<name>VANDROVCOVA, Jana</name>
</author>
<author>
<name>VITOBELLO, Antonio</name>
</author>
<author>
<name>VOS, Janet</name>
</author>
<author>
<name>VYHNÁLKOVÁ, Emílie</name>
</author>
<author>
<name>WIJNGAARD, Robin</name>
</author>
<author>
<name>WILKE, Carlo</name>
</author>
<author>
<name>WILLIAM, Doreen</name>
</author>
<author>
<name>XU, Jishu</name>
</author>
<author>
<name>YALDIZ, Burcu</name>
</author>
<author>
<name>ZALATNAI, Luca</name>
</author>
<author>
<name>ZUREK, Birte</name>
</author>
<author>
<name>BROOKES, Anthony J</name>
</author>
<author>
<name>EVANGELISTA, Teresinha</name>
</author>
<author>
<name>GILISSEN, Christian</name>
</author>
<author>
<name>GRAESSNER, Holm</name>
</author>
<author>
<name>HOOGERBRUGGE, Nicoline</name>
</author>
<author>
<name>OSSOWSKI, Stephan</name>
</author>
<author>
<name>RIESS, Olaf</name>
</author>
<author>
<name>SCHÜLE, Rebecca</name>
</author>
<author>
<name>SYNOFZIK, Matthis</name>
</author>
<author>
<name>VERLOES, Alain</name>
</author>
<author>
<name>MATALONGA, Leslie</name>
</author>
<author>
<name>BRUNNER, Han G</name>
</author>
<author>
<name>LOHMANN, Katja</name>
</author>
<author>
<name>DE VOER, Richarda M</name>
</author>
<author>
<name>TÖPF, Ana</name>
</author>
<author>
<name>VISSERS, Lisenka E L M</name>
</author>
<author>
<name>BELTRAN, Sergi</name>
</author>
<author>
<name>HOISCHEN, Alexander</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/206781</id>
<updated>2025-05-30T08:23:29Z</updated>
<published>2025-01-17T00:00:00Z</published>
<summary type="text">LAURIE, Steven; STEYAERT, Wouter; DE BOER, Elke; POLAVARAPU, Kiran; SCHUERMANS, Nika; SOMMER, Anna K; DEMIDOV, German; ELLWANGER, Kornelia; PARAMONOV, Ida; THOMAS, Coline; ARETZ, Stefan; BAETS, Jonathan; BENETTI, Elisa; BULLICH, Gemma; CHINNERY, Patrick F; CLAYTON-SMITH, Jill; COHEN, Enzo; DANIS, Daniel; DE SAINTE AGATHE, Jean-Madeleine; DENOMMÉ-PICHON, Anne-Sophie; DIAZ-MANERA, Jordi; EFTHYMIOU, Stephanie; FAIVRE, Laurence; FERNANDEZ-CALLEJO, Marcos; FREEBERG, Mallory; GARCIA-PELAEZ, José; GUILLOT-NOEL, Lena; HAACK, Tobias B; HANNA, Mike; HENGEL, Holger; HORVATH, Rita; HOULDEN, Henry; JACKSON, Adam; JOHANSSON, Lennart; JOHARI, Mridul; KAMSTEEG, Erik-Jan; KELLNER, Melanie; KLEEFSTRA, Tjitske; LACOMBE, Didier; LOCHMÜLLER, Hanns; LÓPEZ-MARTÍN, Estrella; MACAYA, Alfons; MARCÉ-GRAU, Anna; MAVER, Aleš; MORSY, Heba; MUNTONI, Francesco; MUSACCHIA, Francesco; NELSON, Isabelle; NIGRO, Vincenzo; OLIMPIO, Catarina; OLIVEIRA, Carla; PAULASOVÁ SCHWABOVÁ, Jaroslava; PAULY, Martje G; PETERLIN, Borut; PETERS, Sophia; PFUNDT, Rolph; PILUSO, Giulio; PISCIA, Davide; POSADA, Manuel; REICH, Selina; RENIERI, Alessandra; RYBA, Lukas; ŠABLAUSKAS, Karolis; SAVARESE, Marco; SCHÖLS, Ludger; SCHÜTZ, Leon; STEINKE-LANGE, Verena; STEVANIN, Giovanni; STRAUB, Volker; STURM, Marc; SWERTZ, Morris A; TARTAGLIA, Marco; TE PASKE, Iris B A W; THOMPSON, Rachel; TORELLA, Annalaura; TRAINOR, Christina; UDD, Bjarne; VAN DE VONDEL, Liedewei; VAN DE WARRENBURG, Bart; VAN REEUWIJK, Jeroen; VANDROVCOVA, Jana; VITOBELLO, Antonio; VOS, Janet; VYHNÁLKOVÁ, Emílie; WIJNGAARD, Robin; WILKE, Carlo; WILLIAM, Doreen; XU, Jishu; YALDIZ, Burcu; ZALATNAI, Luca; ZUREK, Birte; BROOKES, Anthony J; EVANGELISTA, Teresinha; GILISSEN, Christian; GRAESSNER, Holm; HOOGERBRUGGE, Nicoline; OSSOWSKI, Stephan; RIESS, Olaf; SCHÜLE, Rebecca; SYNOFZIK, Matthis; VERLOES, Alain; MATALONGA, Leslie; BRUNNER, Han G; LOHMANN, Katja; DE VOER, Richarda M; TÖPF, Ana; VISSERS, Lisenka E L M; BELTRAN, Sergi; HOISCHEN, Alexander
</summary>
<dc:date>2025-01-17T00:00:00Z</dc:date>
</entry>
<entry>
<title>Macrophages recycle phagocytosed bacteria to fuel immunometabolic responses.</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/206780" rel="alternate"/>
<author>
<name>LESBATS, Juliette</name>
</author>
<author>
<name>BRILLAC, Aurélia</name>
</author>
<author>
<name>REISZ, Julie A</name>
</author>
<author>
<name>MUKHERJEE, Parnika</name>
</author>
<author>
<name>LHUISSIER, Charlène</name>
</author>
<author>
<name>FERNÁNDEZ-MONREAL, Mónica</name>
</author>
<author>
<name>DUPUY, Jean-William</name>
</author>
<author>
<name>SEQUEIRA, Angèle</name>
</author>
<author>
<name>TIOLI, Gaia</name>
</author>
<author>
<name>DE LA CALLE ARREGUI, Celia</name>
</author>
<author>
<name>PINSON, Benoît</name>
</author>
<author>
<name>WENDISCH, Daniel</name>
</author>
<author>
<name>ROUSSEAU, Benoit</name>
</author>
<author>
<name>EFEYAN, Alejo</name>
</author>
<author>
<name>SANDER, Leif Erik</name>
</author>
<author>
<name>D'ALESSANDRO, Angelo</name>
</author>
<author>
<name>GARAUDE, Johan</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/206780</id>
<updated>2025-05-30T08:06:07Z</updated>
<published>2025-04-01T00:00:00Z</published>
<summary type="text">LESBATS, Juliette; BRILLAC, Aurélia; REISZ, Julie A; MUKHERJEE, Parnika; LHUISSIER, Charlène; FERNÁNDEZ-MONREAL, Mónica; DUPUY, Jean-William; SEQUEIRA, Angèle; TIOLI, Gaia; DE LA CALLE ARREGUI, Celia; PINSON, Benoît; WENDISCH, Daniel; ROUSSEAU, Benoit; EFEYAN, Alejo; SANDER, Leif Erik; D'ALESSANDRO, Angelo; GARAUDE, Johan
</summary>
<dc:date>2025-04-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Antenatal phenotype associated with PAK2 pathogenic variants: bilateral pleural effusion as a warning sign.</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/206779" rel="alternate"/>
<author>
<name>DOMENACH, Louis</name>
</author>
<author>
<name>ROORYCK, Caroline</name>
</author>
<author>
<name>LEGENDRE, Marine</name>
</author>
<author>
<name>BOUCHGHOUL, Hanane</name>
</author>
<author>
<name>BENETEAU, Claire</name>
</author>
<author>
<name>MARGOT, Henri</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/206779</id>
<updated>2025-05-30T07:40:08Z</updated>
<published>2025-02-24T00:00:00Z</published>
<summary type="text">DOMENACH, Louis; ROORYCK, Caroline; LEGENDRE, Marine; BOUCHGHOUL, Hanane; BENETEAU, Claire; MARGOT, Henri
</summary>
<dc:date>2025-02-24T00:00:00Z</dc:date>
</entry>
<entry>
<title>Novel variants in FOXI3 gene confirm its implication in Oculo-Auriculo-Vertebral spectrum.</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/206778" rel="alternate"/>
<author>
<name>SEQUEIRA, Angele</name>
</author>
<author>
<name>SAGARDOY, Thomas</name>
</author>
<author>
<name>BOURGEADE, Laetitia</name>
</author>
<author>
<name>LACOMBE, Didier</name>
</author>
<author>
<name>SARRAZIN, Elizabeth</name>
</author>
<author>
<name>TOUTAIN, Annick</name>
</author>
<author>
<name>ROORYCK, Caroline</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/206778</id>
<updated>2025-05-30T07:23:04Z</updated>
<published>2025-05-01T00:00:00Z</published>
<summary type="text">SEQUEIRA, Angele; SAGARDOY, Thomas; BOURGEADE, Laetitia; LACOMBE, Didier; SARRAZIN, Elizabeth; TOUTAIN, Annick; ROORYCK, Caroline
</summary>
<dc:date>2025-05-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Dépistage génétique néonatal: à propos du programme pilote sur l'amyotrophie spinale (DEPISMA)</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/206044" rel="alternate"/>
<author>
<name>LACOMBE, Didier</name>
</author>
<author>
<name>CALMELS, Nadège</name>
</author>
<author>
<name>ANDRE, Carole</name>
</author>
<author>
<name>REBOUL, Marie-Pierre</name>
</author>
<author>
<name>BIANCALANA, Valérie</name>
</author>
<author>
<name>BITOUN, Anaïs</name>
</author>
<author>
<name>COTTET, Christian</name>
</author>
<author>
<name>DE CASTELMUR, Marie</name>
</author>
<author>
<name>HAUSHALTER, Virginie</name>
</author>
<author>
<name>HELOT, Isabelle</name>
</author>
<author>
<name>NOURISSON, Elsa</name>
</author>
<author>
<name>PHILIPPE, Elodie</name>
</author>
<author>
<name>POMMIER, Valentine</name>
</author>
<author>
<name>ARVEILER, Benoit</name>
</author>
<author>
<name>NABARETTE, Hervé</name>
</author>
<author>
<name>DE FERAUDY, Yvan</name>
</author>
<author>
<name>RACLET, Virginie</name>
</author>
<author>
<name>RAMOUSSET, Carole</name>
</author>
<author>
<name>RENEAUD, Hélène</name>
</author>
<author>
<name>RICHARD, Hugo</name>
</author>
<author>
<name>ROMAIN, Sarah</name>
</author>
<author>
<name>BOUFFARD-DUBEAU, Catherine</name>
</author>
<author>
<name>POMIES, Christine</name>
</author>
<author>
<name>ATTARIAN, Shahram</name>
</author>
<author>
<name>STALENS, Caroline</name>
</author>
<author>
<name>VAIDIE, Amandine</name>
</author>
<author>
<name>ESPIL-TARIS, Caroline</name>
</author>
<author>
<name>LAUGEL, Vincent</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/206044</id>
<updated>2025-04-08T14:48:14Z</updated>
<published>2024-01-01T00:00:00Z</published>
<summary type="text">Dépistage génétique néonatal: à propos du programme pilote sur l'amyotrophie spinale (DEPISMA)
LACOMBE, Didier; CALMELS, Nadège; ANDRE, Carole; REBOUL, Marie-Pierre; BIANCALANA, Valérie; BITOUN, Anaïs; COTTET, Christian; DE CASTELMUR, Marie; HAUSHALTER, Virginie; HELOT, Isabelle; NOURISSON, Elsa; PHILIPPE, Elodie; POMMIER, Valentine; ARVEILER, Benoit; NABARETTE, Hervé; DE FERAUDY, Yvan; RACLET, Virginie; RAMOUSSET, Carole; RENEAUD, Hélène; RICHARD, Hugo; ROMAIN, Sarah; BOUFFARD-DUBEAU, Catherine; POMIES, Christine; ATTARIAN, Shahram; STALENS, Caroline; VAIDIE, Amandine; ESPIL-TARIS, Caroline; LAUGEL, Vincent
L’amyotrophie spinale infantile (SMA) liée au gène SMN1 est une maladie génétique neuromusculaire caractérisée par une perte des motoneurones de la corne antérieure de la moelle épinière. La transmission de la maladie se fait sur un mode héréditaire de type autosomique récessif. Dans 95 % des cas, on observe une délétion homozygote de l’exon 7 des 2 gènes SMN1 du patient. Un gène homologue au gène SMN1, le gène SMN2, est peu fonctionnel, en raison d’un épissage de l’exon 7, mais la sévérité de la maladie dépend en partie du nombre variable de copies du gène SMN2. On distingue 4 types cliniques de SMA. Au total, 60 % des SMA de type 1 décèdent avant l’âge de 18 mois. Récemment, trois médicaments ont vu le jour dans la SMA. Le Nusinersen est un oligonucléotide anti-sens, capable de fonctionnaliser le gène SMN2. Il est administré par injections intrathécales répétées. Ce médicament a l’AMM en France pour la prise en charge des types 1, 2 et 3 et a une autorisation pour le traitement présymptomatique de la SMA jusqu’à 3 copies SMN2, indication identique pour la thérapie génique (Onasemnogene abeparvovec, Zolgensma®). Il s’agit d’une injection IV unique. Le Risdiplam, en prise orale quotidienne, est un modificateur d’épissage d’ARN qui a récemment obtenu l’AMM pour le traitement pré-symptomatique. La SMA remplit les critères de Wilson (test génétique fiable, bonne connaissance de la maladie, possibilités thérapeutiques, etc.). Le bénéfice est meilleur lors d’une administration précoce, d’où l’intérêt de la réflexion sur un dépistage néonatal (DNN). Le DNN est disponible à Taiwan, en Belgique, en Allemagne, au Japon, en Australie et aux États-Unis. En France, un projet pilote est en cours depuis début 2023 avec l’AFM-Téléthon dans 2 régions (Nouvelle-Aquitaine et Grand Est), ce qui représente 2 × 55 000 naissances/an, soit 32 enfants atteints de SMA attendus sur 2 ans. Le test de dépistage repose sur la recherche de la délétion homozygote du gène SMN1 par technique de biologie moléculaire. En cas de positivité, un nouveau prélèvement à visé diagnostique sera réalisé pour étudier le nombre de copies SMN2. Une fois le diagnostic confirmé et l’annonce réalisée, le dossier du patient sera passé en RCP, afin de définir les modalités thérapeutiques, selon le phénotype et le nombre de copies SMN2.
</summary>
<dc:date>2024-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>A cognitive and sensory approach based on workshops using the zebrafish model promotes the discovery of life sciences in the classroom</title>
<link href="https://oskar-bordeaux.fr/handle/20.500.12278/206041" rel="alternate"/>
<author>
<name>BOURCIER, Laure M</name>
</author>
<author>
<name>BABIN, Patrick J.</name>
</author>
<id>https://oskar-bordeaux.fr/handle/20.500.12278/206041</id>
<updated>2025-05-30T08:41:12Z</updated>
<published>2024-12-06T00:00:00Z</published>
<summary type="text">BOURCIER, Laure M; BABIN, Patrick J.
The main objective of the ZebraCool programme was to create a positive attitude and curiosity towards science by bringing experimental activities within schools using an introductory cognitive and sensory approach. This innovative programme was offered at all levels of primary and secondary education including vocational high schools. Thematic workshops can be carried out on various themes such as comparative anatomy and embryology, molecular biology and evolution, or toxicology and endocrine disruptors. They were on an ad hoc basis or as part of an annual school project using zebrafish as a model. This animal was a very attractive entry point for the educator to motivate students to appreciate biology, in particular in the field of molecular biology and evolution. For each practical workshop, the student was an actor in his/her learning, which was intended to arouse the curiosity and desire to understand and learn. The programme was based on close collaboration between class teachers and programme educators to adapt workshops' content to the school curriculum. Students conducted their own experiments, formulated and tested hypotheses, learned laboratory techniques, collected, and analysed data. ZebraCool scientific activities fell within a conceptual framework of evolutionary biology through which participants perceived their own inner fish through the comparison of biological processes between humans and zebrafish.
</summary>
<dc:date>2024-12-06T00:00:00Z</dc:date>
</entry>
</feed>
