Identification and characterization of novel mutations implicated in congenital fibrinogen disorders
Smith, Natalie, Bornikova, Larissa, Noetzli, Leila, Guglielmone, Hugo, Minoldo, Salvador, Backos, Donald S., Jacobson, Linda, Thornburg, Courtney D., Escobar, Miguel, White‐Adams, Tara C., Wolberg, Alisa S., Manco‐Johnson, Marilyn, Di Paola, Jorge
Published in Research and practice in thrombosis and haemostasis (01.10.2018)
Published in Research and practice in thrombosis and haemostasis (01.10.2018)
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Journal Article
Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)
Girolami, Antonio, Minoldo, Salvador, Ferrari, Silvia, Colussi, Diego, Lombardi, Anna Maria, Guglielmone, Hugo
Published in Cardiovascular & hematological disorders drug targets (01.08.2017)
Published in Cardiovascular & hematological disorders drug targets (01.08.2017)
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Journal Article
Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2
Zhang, Bin, McGee, Beth, Yamaoka, Jennifer S., Guglielmone, Hugo, Downes, Katharine A., Minoldo, Salvador, Jarchum, Gustavo, Peyvandi, Flora, de Bosch, Norma B., Ruiz-Saez, Arlette, Chatelain, Bernard, Olpinski, Marian, Bockenstedt, Paula, Sperl, Wolfgang, Kaufman, Randal J., Nichols, William C., Tuddenham, Edward G.D., Ginsburg, David
Published in Blood (01.03.2006)
Published in Blood (01.03.2006)
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Journal Article
Tissue Factor and Cancer Procoagulant as Predictors of Thrombosis or Progression in Cancer Patients
Molnar, Soledad, Guglielmone, Hugo, Minoldo, Salvador, Rizzi, Maria L., Lavarda, Marcelo, Jarchum, Gustavo
Published in Blood (16.11.2007)
Published in Blood (16.11.2007)
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