Segmental schwannomatosis: characteristics in 12 patients

per Alaidarous, Abdulqader, Parfait, Beatrice, Ferkal, Salah, Cohen, Joëlle, Wolkenstein, Pierre, Mazereeuw-Hautier, Juliette
Publicat a Orphanet J Rare Dis (2019)

A deletion causing NF2 exon 9 skipping is associated with familial autosomal dominant intramedullary ependymoma

per Zemmoura, Ilyess, Vourc'h, Patrick, Paubel, Agathe, Parfait, Béatrice, Cohen, Joëlle, Bilan, Frédéric, Kitzis, Alain, Rousselot, Cécilia, Parker, Fabrice, François, Patrick, Andres, Christian R.
Publicat 2014

Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis

per Louvrier, Camille, Pasmant, Eric, Briand-Suleau, Audrey, Cohen, Joëlle, Nitschké, Patrick, Nectoux, Juliette, Orhant, Lucie, Zordan, Cécile, Goizet, Cyril, Goutagny, Stéphane, Lallemand, Dominique, Vidaud, Michel, Vidaud, Dominique, Kalamarides, Michel, Parfait, Béatrice
Publicat a Neuro Oncol (2018)

Loss of SMARCE1 expression is a specific diagnostic marker of clear cell meningioma: a comprehensive immunophenotypical and molecular analysis

per Tauziede‐Espariat, Arnault, Parfait, Béatrice, Besnard, Aurore, Lacombe, Joëlle, Pallud, Johan, Tazi, Sanaa, Puget, Stéphanie, Lot, Guillaume, Terris, Benoît, Cohen, Joëlle, Vidaud, Michel, Figarella‐Branger, Dominique, Monnien, Franck, Polivka, Marc, Adle‐Biassette, Homa, Varlet, Pascale
Publicat a Brain Pathol (2017)