Infantile pyknocytosis, a rare cause of hemolytic anemia in newborns: report of two cases in twin girls and literature overview

Por El Nabouch, Mohamad, Rakotoharinandrasana, Iarolalao, Ndayikeza, Alexis, Picard, Véronique, Kayemba-Kay’s, Simon
Publicado no Clin Case Rep (2015)

Testing for hereditary spherocytosis: a French experience

Por Mayeur-Rousse, Caroline, Gentil, Mélanie, Botton, Jérémie, Thibaut, Madeleine Fénéant, Guitton, Corinne, Picard, Véronique
Publicado em 2012

Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study

Por Pincez, Thomas, Guitton, Corinne, Gauthier, Frédéric, de Lambert, Guénolée, Picard, Véronique, Fénéant-Thibault, Madeleine, Turhan, Ali, Mohandas, Narla, Tchernia, Gil, Garçon, Loïc
Publicado no Blood (2016)

Dehydrated Hereditary Stomatocytosislinked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

Por Albuisson, Juliette, Murthy, Swetha E., Bandell, Michael, Coste, Bertrand, Louis-dit-Picard, Hélène, Mathur, Jayanti, Fénéant-Thibault, Madeleine, Tertian, Gérard, de Jaureguiberry, Jean-Pierre, Syfuss, Pierre-Yves, Cahalan, Stuart, Garçon, Loic, Toutain, Fabienne, Rohrlich, Pierre Simon, Delaunay, Jean, Picard, Véronique, Jeunemaitre, Xavier, Patapoutian, Ardem
Publicado em 2013