IRIS

Sfoglia per Titolo

Opzioni
Vai a: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Mostrati risultati da 4.915 a 4.934 di 25.378
Titolo Data di pubblicazione Autore(i) File
Confounding and bias in observational studies in inflammatory bowel disease: a meta-epidemiological study 1-gen-2020 Piovani, Daniele; Pansieri, Claudia; Peyrin-Biroulet, Laurent; Danese, Silvio; Bonovas, Stefanos
Confounding factors in the assessment of oral mucositis in head and neck cancer 1-gen-2022 Lorini, Luigi; Perri, Francesco; Vecchio, Stefania; Belgioia, Liliana; Vinches, Marie; Brana, Irene; Elad, Sharon; Bossi, Paolo
Confronto tra duodenocefalopancreasectomia classica e con conservazione del piloro 1-gen-1994 Zerbi, A; Balzano, G; Patuzzo, R; Di Carlo, V
Confronto tra il valore prognostico della spect miocardica dopo somministrazione di nitrati e l'imaging metabolico con la pet nei pazienti con cardiopatia ischemica e disfunzione ventricolare sinistra 1-gen-2004 Ricci, F; Evangelista, L; Acampa, W; Ferro, A; Mainolfi, C.
Confronto tra la caratterizzazione della placca coronarica alla TC multistrato e la perfusione miocardica alla SPECT in pazienti con sospetta cardiopatia ischemica 1-gen-2009 Evangelista, L; Daniele, S; Acampa, W; Imbriaco, M; Pellegrino, T; Messalli, G; Xhoxhi, E; Pagano, C; Fiumara, G; Di Giorgio, E; Simeone, R; Cuocolo, A
Congelamento di ovociti ed embrioni dopo la sentenza 151 della Corte Costituzionale 1-gen-2010 Zannoni, E; Baggiani, A; Drovanti, A; Sacchi, L; De Cesare, R; Specchia, C; Bergamasco, P; Arfuso, V; Levi Setti, P
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene 1-gen-2004 Spena, S; Duga, S; Asselta, R; Peyvandi, F; Mahasandana, C; Malcovati, M; Tenchini, Ml
Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management 1-gen-2021 Simurda, Tomas; Asselta, Rosanna; Zolkova, Jana; Brunclikova, Monika; Dobrotova, Miroslava; Kolkova, Zuzana; Loderer, Dusan; Skornova, Ingrid; Hudecek, Jan; Lasabova, Zora; Stasko, Jan; Kubisz, Peter
Congenital afibrinogenemia caused by uniparental isodisomy of chromosome 4 containing a 15-kb deletion involving fibrinogen Aalpha-chain gene 1-gen-2004 Spena, S; Duga, S; Asselta, R; Malcovati, M; Tenchini, Ml
Congenital afibrinogenemia, identification of four novel homozygous mutations in the fibrinogen gene cluster: three point mutations and a 15-kb deletion 1-gen-2003 Duga, S; Asselta, R; Spena, S; Peyvandi, F; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bb-chain gene causing activation of cryptic splice sites 1-gen-2002 Spena, S; Duga, S; Asselta, R; Malcovati, M; Peyvandi, F; Tenchini, Ml
Congenital afibrinogenemia: identification of five new point mutations leading to Aalpha-chain truncations 1-gen-2000 Duga, S; Asselta, R; Santagostino, E; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: In Vitro Expression of Two Novel Missense Mutations in the Fibrinogen Bbeta-Chain Gene Demonstrates That One of Them Acts as a Splicing Mutation 1-gen-2002 Asselta, R; Spena, S; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene 1-gen-2003 Spena, S; Asselta, R; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene 1-gen-2006 Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml; Duga, S
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs 1-gen-2001 Asselta, R; Duga, S; Spena, S; Santagostino, E; Peyvandi, F; Piseddu, G; Targhetta, R; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: two novel fibrinogen gene mutations identified in two patients from Iran 1-gen-2006 Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml
Congenital factor XI deficiency: an update. 1-gen-2013 Duga, S; Salomon, O.
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database 1-gen-2024 Mohsenian, Samin; Palla, Roberta; Menegatti, Marzia; Cairo, Andrea; Lecchi, Anna; Casini, Alessandro; Neerman-Arbez, Marguerite; Asselta, Rosanna; Scardo, Sara; Siboni, Simona Maria; Blatný, Jan; Zapletal, Ondrej; Schved, Jean-Francois; Giansily-Blaizot, Muriel; Halimeh, Susan; Daoud, Ayman; Platokouki, Helen; Pergantou, Helen; Schutgens, Roger E G; Haaften-Spoor, Monique Van; Brons, Paul; Laros-van Gorkom, Britta A P; Pinxten, Elise Van; Borhany, Munira; Fatima, Naveena; Mikovic, Danijela; Saracevic, Marko; Özdemir, Gül Nihal; Ay, Yılmaz; Makris, Michael; Lockley, Caryl; Mumford, Andrew D; Harvey, Andrew; Austin, Steven Kenneth; Shapiro, Amy D; Williamson, Adrianna; Mcguinn, Catherine; Goldberg, Ilene; de Moerloose, Philippe; Peyvandi, Flora
Congenital Heart Defects in IVF/ICSI Pregnancy: Systematic Review and Meta-analysis 1-gen-2018 Giorgione, V.; Parazzini, F.; Fesslova, V.; Cipriani, S.; Candiani, M.; Inversetti, A.; Sigismondi, C.; Tiberio, F.; Cavoretto, P.
Mostrati risultati da 4.915 a 4.934 di 25.378
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile