In vitro effects of loratadine and its active metabolite an T lymphocytes
1998-01-01 Cagnoni, F.; Mincarini, M.; Passalacqua, G.; Semino, C.; Pietra, G.; Melioli, G.; Canonica, G. W.
State of the art of rare bleeding disorders database (RBDD)
2008-01-01 Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F.
A Published Pharmacogenetic Algorithm Was Poorly Predictive of Tacrolimus Clearance in An Independent Cohort of Renal Transplant Recipients
2012-01-01 Boughton, O; Borgulya, G; Cecconi, M; Macphee, Iam
The lymphatic system controls intestinal inflammation and inflammation-associated colon cancer through the chemokine decoy receptor D6
2009-01-01 Vetrano, S.; Borroni, E.; Bonecchi, R.; Correale, C.; Sarukhan, A.; Vincenzo, A.; Fantini, M.; Roncalli, M.; Malesci, A.; Vecchi, A.; Mantovani, A.; Locati, M.; Danese, S.
Low risk of hepatitis B reactivation in patients with chronic hepatitis C and concurrent inactive hepatitis B infection treated with interferon and ribavirin
2008-01-01 Iavarone, M.; Aghemo, A.; Viganò, M.; Rumi, M. G.; Agnelli, F.; Lampertico, P.; Donato, M. F.; Colombo, M.
In vivo and in vitro effect of ribavirin and interferon on erythropoiesis in patients with hepatitis C
2009-01-01 Ronzoni, L.; Colancecco, A.; Cattaneo, A.; Aghemo, A.; Monico, S.; Rumi, M.; Colombo, M.; Cappellini, M. D.
Five new point mutations in fibrinogen alpha-chain gene causing afibrinogenemia
2000-01-01 Asselta, R; Duga, S; Malcovati, M; Simonic, T; Santagostino, E; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: two novel fibrinogen gene mutations identified in two patients from Iran
2006-01-01 Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml
CHRNA3/CHRNA5/CHRNB4 cluster and autosomal dominant nocturnal frontal lobe epilepsy
2000-01-01 Bonati, Mt; Asselta, R; Duga, S; Malcovati, M; Tenchini, Ml; Oldani, A; Zucconi, M; Ferini-Strambi, L; Dalprà, L
Molecular genetic analysis of coagulation factor XI deficiency in Italian patients
2003-01-01 Zadra, G; Asselta, R; Santagostino, E; Mannucci, Pm; Malcovati, M; Tenchini, Ml; Duga, S
Severe factor V deficiency: identification and molecular characterization of three novel splicing mutations
2006-01-01 Asselta, R; Dall’Osso, C; Duga, S; Locatelli, N; Malcovati, M; 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
2002-01-01 Asselta, R; Spena, S; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml
Two cases of congenital afibrinogenemia caused by potentially elusive mutations
2003-01-01 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
2003-01-01 Duga, S; Asselta, R; Spena, S; Peyvandi, F; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Characterization of the F11 alternative splicing pattern: identification of a novel coagulation FXI isoform
2007-01-01 Guella, I; Asselta, R; Rimoldi, V; Tenchini, Ml; Duga, S
A novel mechanism for congenital afibrinogenemia based on pseudoexon activation in the fibrinogen gamma-chain gene
2007-01-01 Spena, S; Asselta, R; Platè, M; Castaman, G; Duga, S; Tenchini, Ml
Eight novel mutations in FXI gene
2005-01-01 G., Castaman; R., Ghiotto; G., Rossetti; D., Habart; A., Tagliaferri; Duga, S
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients
2009-01-01 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
Characterization of productive and unproductive mRNA splicings in F11: identification of a novel coagulation FXI isoform
2008-01-01 Rimoldi, V; Guella, I; Asselta, R; De Cristofaro, R; Peyvandi, F; Mannucci, Pm; Duga, S
Anemia during peginterferon-ribavirin therapy results from both increased suppression of erythroid differentiation and haemolysis
2008-01-01 Aghemo, A.; Ronzoni, L.; Rumi, M.; Monico, S.; Colancecco, A.; Grillo, P.; Viganò, M.; Cappellini, M. D.; Colombo, M.
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
Scopri
Tipologia
- 1 Contributo su Rivista2151
Data di pubblicazione
- 2020 - 2026113
- 2010 - 20191340
- 2000 - 2009587
- 1990 - 1999110
- 1988 - 19891
Editore
- Nature Publishing Group4
- s.n4
- ICRS3
- Blackwell1
Rivista
- EUROPEAN UROLOGY. SUPPLEMENTS124
- GASTROENTEROLOGY123
- EUROPEAN JOURNAL OF NUCLEAR MEDIC...120
- THE JOURNAL OF UROLOGY111
- DIGESTIVE AND LIVER DISEASE100
- THE JOURNAL OF NUCLEAR MEDICINE80
- ANNALS OF THE RHEUMATIC DISEASES69
- RADIOTHERAPY AND ONCOLOGY59
- ANNALS OF ONCOLOGY57
- JOURNAL OF CLINICAL ONCOLOGY45
Keyword
- Myelodysplastic syndrome8
- Survival4
- biomimetic3
- Mitochondrial ferritin3
- osteochondral3
- Prognosis3
- scaffold3
- Sideroblastic anemia3
- viscosupplementation3
- COLONOSCOPIC SURVEILLANCE2
Lingua
- eng794
- ita24
- und6
Accesso al fulltext
- no fulltext2098
- reserved51
- open2