Isolated Cerebral Alveolar Echinococcosis

por Baldolli, Aurélie, Bonhomme, Julie, Yera, Hélène, Grenouillet, Frederic, Chapon, Françoise, Barbier, Charlotte, Hazera, Pascal, Verdon, Renaud
Publicado 2018

Lymphomatoid Granulomatosis Treated Successfully with Rituximab in a Renal Transplant Patient

por Castrale, Cindy, El Haggan, Wael, Chapon, Françoise, Reman, Oumedaly, Lobbedez, Thierry, Ryckelynck, Jean Philippe, Hurault de Ligny, Bruno
Publicado 2011

Glycogenin-1 deficiency mimicking limb-girdle muscular dystrophy

por Lefeuvre, Claire, Schaeffer, Stéphane, Carlier, Robert-Yves, Fournier, Maxime, Chapon, Françoise, Biancalana, Valérie, Nicolas, Guillaume, Malfatti, Edoardo, Laforêt, Pascal
Publicado 2020

Developmental timing of CCM2 loss influences cerebral cavernous malformations in mice

por Boulday, Gwénola, Rudini, Noemi, Maddaluno, Luigi, Blécon, Anne, Arnould, Minh, Gaudric, Alain, Chapon, Françoise, Adams, Ralf H., Dejana, Elisabetta, Tournier-Lasserve, Elisabeth
Publicado 2011

Trisomy 19 ependymoma, a newly recognized genetico-histological association, including clear cell ependymoma

por Rousseau, Emmanuel, Palm, Thomas, Scaravilli, Francesco, Ruchoux, Marie-Magdeleine, Figarella-Branger, Dominique, Salmon, Isabelle, Ellison, David, Lacroix, Catherine, Chapon, Françoise, Mikol, Jacqueline, Vikkula, Miikka, Godfraind, Catherine
Publicado 2007

Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome

por Snanoudj, Sarah, Mordel, Patrick, Dupas, Quentin, Schanen, Cécile, Arion, Alina, Gérard, Marion, Read, Marie‐Hélène, Nait Rabah, Djamel, Goux, Didier, Chapon, Françoise, Jokic, Mickael, Allouche, Stéphane
Publicado 2019

Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies

por Vadrot, Nathalie, Ader, Flavie, Moulin, Maryline, Merlant, Marie, Chapon, Françoise, Gandjbakhch, Estelle, Labombarda, Fabien, Maragnes, Pascale, Réant, Patricia, Rooryck, Caroline, Probst, Vincent, Donal, Erwan, Richard, Pascale, Ferreiro, Ana, Buendia, Brigitte
Publicado 2023

Sustained Response and Rationale of Programmed Cell Death-1-Targeting for Progressive Multifocal Leukoencephalopathy

por Audemard-Verger, Alexandra, Gasnault, Jacques, Faisant, Maxime, Besse, Marie-Catherine, Martin-Silva, Nicolas, Berra, Mado, Fournier, Luc, Boutemy, Jonathan, Maigne, Gwenola, De Boysson, Hubert, Ruet, Alexis, Vabret, Astrid, Chapon, Françoise, Martin-Blondel, Guillaume, Aouba, Achille
Publicado 2019

Novel dominant distal titinopathy phenotype associated with copy number variation

por Perrin, Aurélien, Juntas Morales, Raul, Chapon, Françoise, Thèze, Corinne, Lacourt, Delphine, Pégeot, Henri, Uro‐Coste, Emmanuelle, Giovannini, Diane, Leboucq, Nicolas, Mallaret, Martial, Lagrange, Emmeline, Rigau, Valérie, Gaudon, Karen, Richard, Pascale, Koenig, Michel, Métay, Corinne, Cossée, Mireille
Publicado 2021

Multimodal evaluation of hypoxia in brain metastases of lung cancer and interest of hypoxia image-guided radiotherapy

por Corroyer-Dulmont, Aurélien, Valable, Samuel, Fantin, Jade, Chatre, Laurent, Toutain, Jérôme, Teulier, Sylvain, Bazille, Céline, Letissier, Elise, Levallet, Jérôme, Divoux, Didier, Ibazizène, Méziane, Guillouet, Stéphane, Perrio, Cécile, Barré, Louisa, Serres, Sébastien, Sibson, Nicola R., Chapon, Françoise, Levallet, Guénaëlle, Bernaudin, Myriam
Publicado 2021

DCTN1 mutations in Perry syndrome

por Farrer, Matthew J., Hulihan, Mary M., Kachergus, Jennifer M., Dächsel, Justus, Stoessl, A. Jon, Grantier, Linda L., Calne, Susan, Calne, Donald B., Lechevalier, Bernard, Chapon, Francoise, Tsuboi, Yoshio, Yamada, Tatsuo, Gutmann, Ludwig, Elibol, Bülent, Bhatia, Kailash P., Wider, Christian W., Vilariño-Güell, Carles, Ross, Owen A., Brown, Laura A., Castanedes-Casey, Monica, Dickson, Dennis W., Wszolek, Zbigniew K.
Publicado 2009

Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study

por Dogan, Celine, De Antonio, Marie, Hamroun, Dalil, Varet, Hugo, Fabbro, Marianne, Rougier, Felix, Amarof, Khadija, Arne Bes, Marie-Christine, Bedat-Millet, Anne-Laure, Behin, Anthony, Bellance, Remi, Bouhour, Françoise, Boutte, Celia, Boyer, François, Campana-Salort, Emmanuelle, Chapon, Françoise, Cintas, Pascal, Desnuelle, Claude, Deschamps, Romain, Drouin-Garraud, Valerie, Ferrer, Xavier, Gervais-Bernard, Helene, Ghorab, Karima, Laforet, Pascal, Magot, Armelle, Magy, Laurent, Menard, Dominique, Minot, Marie-Christine, Nadaj-Pakleza, Aleksandra, Pellieux, Sybille, Pereon, Yann, Preudhomme, Marguerite, Pouget, Jean, Sacconi, Sabrina, Sole, Guilhem, Stojkovich, Tanya, Tiffreau, Vincent, Urtizberea, Andoni, Vial, Christophe, Zagnoli, Fabien, Caranhac, Gilbert, Bourlier, Claude, Riviere, Gerard, Geille, Alain, Gherardi, Romain K., Eymard, Bruno, Puymirat, Jack, Katsahian, Sandrine, Bassez, Guillaume
Publicado 2016