The Interplay of Exosomes and NK Cells in Cancer Biology

por Batista, Inês A., Quintas, Sofia T., Melo, Sónia A.
Publicado 2021

NGLY1 deficiency—A rare congenital disorder of deglycosylation

por Lipari Pinto, Patrícia, Machado, Catarina, Janeiro, Patrícia, Dupont, Juliette, Quintas, Sofia, Sousa, Ana Berta, Gaspar, Ana
Publicado 2020

Exosomal glypican-1 is elevated in pancreatic cancer precursors and can signal genetic predisposition in the absence of endoscopic ultrasound abnormalities

por Moutinho-Ribeiro, Pedro, Batista, Ines A, Quintas, Sofia T, Adem, Bárbara, Silva, Marco, Morais, Rui, Peixoto, Armando, Coelho, Rosa, Costa-Moreira, Pedro, Medas, Renato, Lopes, Susana, Vilas-Boas, Filipe, Baptista, Manuela, Dias-Silva, Diogo, Esteves, Ana L, Martins, Filipa, Lopes, Joanne, Barroca, Helena, Carneiro, Fátima, Macedo, Guilherme, Melo, Sonia A
Publicado 2022

A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies

por Baumgartner, Tobias, Carreño, Mar, Rocamora, Rodrigo, Bisulli, Francesca, Boni, Antonella, Brázdil, Milan, Horak, Ondrej, Craiu, Dana, Pereira, Cristina, Guerrini, Renzo, San Antonio‐Arce, Victoria, Schulze‐Bonhage, Andreas, Zuberi, Sameer M., Hallböök, Tove, Kalviainen, Reetta, Lagae, Lieven, Nguyen, Sylvie, Quintas, Sofia, Franco, Ana, Cross, J. Helen, Walker, Matthew, Arzimanoglou, Alexis, Rheims, Sylvain, Granata, Tiziana, Canafoglia, Laura, Johannessen Landmark, Cecilie, Sen, Arjune, Rattihalli, Rohini, Nabbout, Rima, Tartara, Elena, Santos, Manuela, Rangel, Rui, Krsek, Pavel, Marusic, Petr, Specchio, Nicola, Braun, Kees P. J., Smeyers, Patricia, Villanueva, Vicente, Kotulska, Katarzyna, Surges, Rainer, Tinuper, Paolo, Licchetta, Laura, Michelucci, Roberto, Toulouse, Joseph, Panagiotakaki, Eleni, Ostrowsky‐Coste, Karine, Lesca, Gaetan, de Curtis, Marco, Elisak, Martin, Domańska‐Pakiea, Dorota, Sadowski, Krzysztof
Publicado 2021