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1.5 Abstract in rivista: [2157] Home page tipologia

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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 961 a 980 di 2.157
Titolo Data di pubblicazione Autore(i) File
Conservative treatment of the spontaneus avascular necrosis of the knee in middle-agedpatients 1-gen-2012 Marcheggiani Muccioli, G. M.; Grassi, A.; Bonazinga, T.; Nitri, M.; Zaffagnini, S.; Marcacci, M.
The optimal type of bolus following a 'Mediterranean' meal in children and adolescents with type 1 diabetes using insulin pump therapy 1-gen-2009 Macedoni, M.; Scaramuzza, A. E.; Iafusco, D.; Spiri, D.; Bosetti, A.; Giani, E.; Gazzarri, A.; Mameli, C.; Fabiano, V.; Depalma, A.; Zuccotti, G. V.
VINORELBINE (V) IN PEMETREXED-PRETREATED PATIENTS (PTS) WITH MALIGNANT PLEURAL MESOTHELIOMA (MPM) 1-gen-2010 De Vincenzo, F; Lorenzi, E; Zucali, Pa; Simonelli, M; Gianoncelli, L; Ceresoli, Gl; Ripa, C; Giordano, L; Santoro, A
Effects of acetylsalicylic acid on adiposity in a mouse model of diet-induced obesity 1-gen-2017 Sommariva, Michele; C., Sardi; Gibelli, DANIELE MARIA; Kallikourdis, Marinos; Rumio, Cristiano
Regulatory T cells and pregnancy 1-gen-2009 Kallikourdis, M
Understanding the WHIM syndrome: molecular analysis of CXCR4 functions in lymphocyte activation 1-gen-2011 Kallikourdis, M; Trovato, Ae; Anselmi, F; Sarukhan, A; Roselli, G; Tassone, L; Badolato, R; Viola, A
In vitro effects of loratadine and its active metabolite an T lymphocytes 1-gen-1998 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) 1-gen-2008 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 1-gen-2012 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 1-gen-2009 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.
In vivo and in vitro effect of ribavirin and interferon on erythropoiesis in patients with hepatitis C 1-gen-2009 Ronzoni, L.; Colancecco, A.; Cattaneo, A.; Aghemo, A.; Monico, S.; Rumi, M.; Colombo, M.; Cappellini, M. D.
Low risk of hepatitis B reactivation in patients with chronic hepatitis C and concurrent inactive hepatitis B infection treated with interferon and ribavirin 1-gen-2008 Iavarone, M.; Aghemo, A.; Viganò, M.; Rumi, M. G.; Agnelli, F.; Lampertico, P.; Donato, M. F.; Colombo, M.
Five new point mutations in fibrinogen alpha-chain gene causing afibrinogenemia 1-gen-2000 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 1-gen-2006 Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml
Molecular genetic analysis of coagulation factor XI deficiency in Italian patients 1-gen-2003 Zadra, G; Asselta, R; Santagostino, E; Mannucci, Pm; Malcovati, M; Tenchini, Ml; Duga, S
CHRNA3/CHRNA5/CHRNB4 cluster and autosomal dominant nocturnal frontal lobe epilepsy 1-gen-2000 Bonati, Mt; Asselta, R; Duga, S; Malcovati, M; Tenchini, Ml; Oldani, A; Zucconi, M; Ferini-Strambi, L; Dalprà, L
Severe factor V deficiency: identification and molecular characterization of three novel splicing mutations 1-gen-2006 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 1-gen-2002 Asselta, R; Spena, S; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml
Two cases of congenital afibrinogenemia caused by potentially elusive mutations 1-gen-2003 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
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 961 a 980 di 2.157
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Scopri
Tipologia
  • 1 Contributo su Rivista2157
Autore
  • OYEN, Willem Jozef Gerard230
  • GUAZZONI, GIORGIO FERRUCCIO161
  • SCORSETTI, Marta128
  • REPICI, Alessandro126
  • ARMUZZI, ALESSANDRO105
  • LUGHEZZANI, Giovanni104
  • SANTORO, Armando87
  • CHITI, ARTURO86
  • BUFFI, Nicolomaria85
  • MANGIAVILLANO, BENEDETTO85
Data di pubblicazione
  • 2020 - 2025111
  • 2010 - 20191343
  • 2000 - 2009591
  • 1990 - 1999111
  • 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
  • eng798
  • ita24
  • und6
Accesso al fulltext
  • no fulltext2104
  • reserved51
  • open2