Sfoglia per Autore  

Opzioni
Mostrati risultati da 1 a 20 di 139
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2002 Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees Semprini, S; Capon, F; Tacconelli, A; Giardina, E; Orecchia, A; Mingarelli, R; Gobello, T; Zambruno, G; Botta, A; Fabrizi, G; Novelli, G Articolo su rivista
1-gen-2002 Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population Borgiani, P; Vallo, L; D'Apice, Mr; Giardina, E; Pucci, S; Capon, F; Nistico', Sp; Chimenti, S; Pallone, F; Novelli, G Articolo su rivista
1-gen-2002 Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre Giardina, E; Capon, F; D'Apice, Mr; Amati, F; Arturi, A; Filetti, S; Bonifazi, E; Pucci, S; Conte, C; Novelli, G Articolo su rivista
1-gen-2003 Genetica Medica Pratica Novelli, G; Giardina, E Monografia
1-gen-2003 Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. Mango, R; Clementi, F; Borgiani, P; Forleo, G; Federici, M; Contino, G; Giardina, E; Garza, L; Fahdi, I; Lauro, R; Mehta, J; Novelli, G; Romeo, F Articolo su rivista
1-gen-2003 Role of genetics in prevention of coronary atherosclerosis Novelli, G; Borgiani, P; Giardina, E; Mango, R; Contino, G; Romeo, F; Mehta, J Articolo su rivista
1-gen-2003 Insight into genetics of atopic dermatitis: future approaches and directions Novelli, G; Giardina, E; Paradisi, M; Pedicelli, C; Girolomoni, G; Nasorri, F; Chimenti, S; Marulli, G; Rossi, P; Moschese, V; Chini, L; Capon, F Articolo su rivista
1-gen-2004 A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 Bonifazi, E; Vallo, L; Giardina, E; Botta, A; Novelli, G Articolo su rivista
1-gen-2004 Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] Sangiuolo, Fc; Filareto, A; Giardina, E; Nardone, A; Pilu, G; Pietropolli, A; Bertini, E; Novelli, G Articolo su rivista
1-mag-2004 Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population Giardina, E; Novelli, G; Costanzo, A; Nisticò, S; Bulli, C; Sinibaldi, C; Sorgi, M; Chimenti, S; Pallone, F; Taccari, E; Borgiani, P Articolo su rivista
1-giu-2004 The psoriasis genetics as a model of complex disease Giardina, E; Sinibaldi, C; Novelli, G Articolo su rivista
1-nov-2004 Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus Giardina, E; Capon, F; De Rosa, M; Mango, R; Zambruno, G; Orecchia, A; Chimenti, S; Giardina, B; Novelli, G Articolo su rivista
1-gen-2005 The long and winding road: Searching for non-MHC psoriasis susceptibility loci Capon, F; Giardina, E Articolo su rivista
1-gen-2005 Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6 Abecasis, G; Allen, M; Barker, J; Burden, D; Capon, F; Christophers, E; Elder, J; Fischer, J; Giardina, E; Gudjonsson, J; Huffmeier, U; Jenisch, S; Karason, A; Kere, J; Nair, R; Novelli, G; Prud'Homme, J; Qin, Z; Samuelsson, L; Sanchez, F; Saarialho Kere, U; Stahle, M; Stuart, P; Tillman, D; Traupe, H; Trembath, R; Valdimarsson, H; Veal, C; Voorhees, J; Weichenthal, M Articolo su rivista
1-gen-2005 Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests Botta, A; Tacconelli, A; Bagni, I; Giardina, E; Bonifazi, E; Pietropolli, A; Clementi, M; Novelli, G Articolo su rivista
1-gen-2006 Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 Giardina, E; Sinibaldi, C; Chini, L; Moschese, V; Marulli, G; Provini, A; Rossi, P; Paradisi, M; Chimenti, S; Galli, E; Brunetti, E; Girolomoni, G; Novelli, G Articolo su rivista
1-gen-2006 PSORS2 markers are not associated with psoriatic arthritis in the Italian population Giardina, E; Predazzi, I; Sinibaldi, C; Peconi, C; Amerio, P; Costanzo, A; Paradisi, A; Capizzi, R; Paradisi, M; Chimenti, S; Taccari, E; Novelli, G Articolo su rivista
1-gen-2006 Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: A genetic study of Sardinian family Concolino, P; Satta, M; Santonocito, C; Carrozza, C; Rocchetti, S; Ameglio, F; Giardina, E; Zuppi, C; Capoluongo, E Articolo su rivista
1-lug-2006 Gonadal mosaicism in hereditary angioedema Guarino, S; Perricone, C; Guarino, Md; Giardina, E; Gambardella, S; D'Apice, Mr; Bulli, C; Perricone, R; Novelli, G Articolo su rivista
1-nov-2006 Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency Porzio, O; Cunsolo, V; Malaponti, M; De Nisco, E; Acquafredda, A; Cavallo, L; Andreani, M; Giardina, E; Testi, M; Cappa, M; Federici, G Articolo su rivista
Mostrati risultati da 1 a 20 di 139
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