Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Chantal Mailloux"'
Autor:
Dorsa Sadat Kiaei, Valerie Larouche, Jean-Claude Décarie, Uri Tabori, Cynthia Hawkins, Sarah Lippe, Benjamin Ellezam, Luis H Ospina, Yves Theoret, Leandra Desjardins, Marie-Elaine Metras, Serge Sultan, Edith Cantin, Marie-Eve Routhier, Chantal Mailloux, Marie-claude Bertrand, Maxime Caru, Tara McKeown, Stephanie Vairy, Geneviève Legault, Eric Bouffet, Vijay Ramaswamy, Hallie Coltin, Lucie Lafay-Cousin, Juliette Hukin, Craig Erker, Nada Jabado, Mathieu Dehaes, Sébastien Perreault
Publikováno v:
Neuro-Oncology. 24:vii70-vii70
BACKGROUND Plexiform neurofibromas (PN) are observed in up to 50% of patients with neurofibromatosis type 1 (NF1). Trametinib has been used widely to treat PN but limited data has been reported on its efficacy within a clinical trial. METHODS This on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eec9d2a13f16f1d043839e0570d5218
https://doi.org/10.1093/neuonc/noac209.271
https://doi.org/10.1093/neuonc/noac209.271
Autor:
Dorsa Sadat Kiaei, Valérie Larouche, Jean-Claude Décarie, Uri Tabori, Cynthia Hawkin, Sarah Lippé, Benjamin Ellezam, Luis H Ospina, Yves Théoret, Léandra Desjardins, Marie-Élaine Métras, Serge Sultan, Édith Cantin, Marie-Ève Routhier, Chantal Mailloux, Marie-Claude Bertrand, Maxime Caru, Stéphanie Vairy, Geneviève Legault, Éric Bouffet, Vijay Ramaswamy, Hallie Coltin, Lucie Lafay-Cousin, Juliette Hukin, Craig Erker, Nada Jabado, Mathieu Dehaes, Sébastien Perreault
Publikováno v:
Neuro-Oncology. 24:i129-i129
BACKGROUND: Plexiform neurofibromas (PN) are found in up to 50% of patients with neurofibromatosis type 1 (NF1). Trametinib has been used widely to treat PN but limited data has been reported on its efficacy within a clinical trial. METHODS: This ong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a3ce9de27d59c5aca9976f0c4504948
https://doi.org/10.1093/neuonc/noac079.472
https://doi.org/10.1093/neuonc/noac079.472
Publikováno v:
Pediatrics. 138(1)
Iron deficiency is a common cause of anemia (IDA) in infancy and can be associated with neurocognitive impairments. Iron-refractory IDA (IRIDA) has recently been described as an inherited cause of IDA due to loss-of-function mutations in the TMPRSS6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afdad1b3d4e7b37d77303f4a7055f561
https://pubmed.ncbi.nlm.nih.gov/27365303
https://pubmed.ncbi.nlm.nih.gov/27365303