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1.5 Abstract in rivista: [2151] Home page tipologia

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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 1.141 a 1.160 di 2.151
Titolo Data di pubblicazione Autore(i) File
LA TECNICA ANTIREFLUSSO DI GONHEIM SU NEOVESCICA ORTOTOPICA DETUBULIZZATA CON SUTURATRICI MECCANICHE 1-gen-1999 Muto, G; Bardari, F; Leggero, R
SPECIFIC CHROMOSOME ABERRATION IN HUMAN RENAL CELL CARCINOMA 1-gen-1991 Muto, G; Moroni, M
LA CISTOPROSTATECTOMIA CON RISPARMIO DELLA CAPSULA, DELLE VESCICOLE SEMINALI ED ILEOCAPSULOPLASTICA: UN ULTERIORE CONTRIBUTO ALLA TERAPIA DELLA COARTAZIONE VESCICALE 1-gen-1999 Muto, G; Bardari, F; Leggero, R
Immunohistochemical study of dermal microvasculature density and vessel basement membrane thickness in Bateman's senile purpura 1-gen-2012 Grassi, S; Concardi, M; Puccio, I; Arbustini, E; Borroni, Rg
Trattamento sequenziale della psoriasi diffusa in placche con 3 farmaci biologici: difficoltà terapeutiche e studio di un caso clinico 1-gen-2011 Cananzi, R; Fornara, L; Manna, G; Carugno, A; Grasso, V; Alborghetti, A; Ronzi, G; Borroni, R; Brazzelli, V
Anti-Fas Ligand neutralizing antibodies prevent acantholysis both in vitro and in vivo 1-gen-2009 Marconi, A; Lotti, R; Truzzi, F; Dallaglio, K; Borroni, R; Palazzo, E; Kitajima, Y; Pincelli, C
Involvement of fibrinogen Bbeta-chain in the pathogenesis of congenital afibrinogenemia 1-gen-2001 Duga, S; Asselta, R; Spena, S; Santagostino, E; Peyvandi, F; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Analysis of association of five newly identified polymorphisms in  and  fibrinogen genes with plasma fibrinogen levels 1-gen-2000 Menegatti, M; Asselta, R; Duga, S; Malcovati, M; Bucciarelli, P; Tenchini, Ml; Mannucci, Pm
Genetics of Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 1-gen-1999 Bonati, Mt; Duga, S; Asselta, R; Malcovati, M; Tenchini, Ml; Ferini-Strambi, L; Zucconi, M; Oldani, A; Dalprà, L
Type II Mutation (Glu117stop) Causes Factor XI Deficiency By Inducing Allele Specific mRNA Degradation 1-gen-2005 Soldà, G; Asselta, R; Ghiotto, R; Malcovati, M; Tenchini, Ml; Castaman, G; Duga, S
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
In-vitro Expression And Functional Characterization Of Four Mutations Causing Factor XI Deficiency 1-gen-2005 Duga, S; Asselta, R; Bozzao, C; Ghiotto, R; Malcovati, M; Tenchini, Ml; Castaman, G
Genetic defects in congenital afibrinogenemia 1-gen-2002 Asselta, R; Spena, S; Duga, S; Tenchini, Ml
Simultaneous genotyping of FXI type II and type III mutations by multiplex real-time PCR in healthy Italians and in FXI-deficient patients 1-gen-2007 Zadra, G; Asselta, R; Tenchini, Ml; Seligsohn, U; Castaman, G; Duga, S
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients 1-gen-2006 Monaldini, L; Duga, S; Asselta, R; Peyvandi, F; Karimi, M; Malcovati, M; Tenchini, Ml
Alternative splicing and nonsense-mediated decay in the F5 gene 1-gen-2007 Dall’Osso, C; Duga, S; Locatelli, N; Peyvandi, F; Tenchini, Ml; Asselta, R
The Protein Kinase C Alpha (PRKCA) gene is associated with multiple sclerosis in the Italian population 1-gen-2009 Asselta, R; Paraboschi, E; Solda, G; Dall’Osso, C; Gemmati, D; Zamboni, P; Benedetti, Md; D’Alfonso, S; Duga, S
Tau and alpha-synuclein and genetic susceptibility to Parkinson Disease in the Italian population 1-gen-2010 Guella, I; Trotta, L; Asselta, R; Solda', G; Zini, M; Zecchinelli, A; Pezzoli, G; Goldwurm, S; Duga, S
hUPF1 and hUPF2 knockdown by RNA interference in HepG2 cells as a model to study nonsense-mediated mRNA decay modulation of coagulation-gene expression 1-gen-2010 Platè, M; Rimoldi, V; Duga, S; Asselta, R
THE USE OF LAPAROSCOPIC DEVICES IN MINI- INVASIVE SURGERY OF THE MEGAURETER 1-gen-1993 Muto, G; Moroni, M
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 1.141 a 1.160 di 2.151
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Scopri
Tipologia
  • 1 Contributo su Rivista2151
Autore
  • OYEN, Willem Jozef Gerard230
  • GUAZZONI, GIORGIO FERRUCCIO161
  • SCORSETTI, Marta128
  • REPICI, Alessandro126
  • ARMUZZI, ALESSANDRO105
  • LUGHEZZANI, Giovanni104
  • SANTORO, Armando87
  • CHITI, ARTURO86
  • BUFFI, Nicolomaria85
  • MANGIAVILLANO, BENEDETTO83
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