CAPON, FRANCESCA
CAPON, FRANCESCA
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13
1999-09-11 Servidei, S; Capon, F; Spinazzola, A; Mirabella, M; Semprini, S; de Rosa, G; Gennarelli, M; Sangiuolo, Fc; Ricci, E; Mohrenweiser, H; Dallapiccola, B; Tonali, P; Novelli, G
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus
2004-11-01 Giardina, E; Capon, F; De Rosa, M; Mango, R; Zambruno, G; Orecchia, A; Chimenti, S; Giardina, B; Novelli, G
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees
2002-01-01 Semprini, S; Capon, F; Tacconelli, A; Giardina, E; Orecchia, A; Mingarelli, R; Gobello, T; Zambruno, G; Botta, A; Fabrizi, G; Novelli, G
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population
2002-01-01 Borgiani, P; Vallo, L; D'Apice, Mr; Giardina, E; Pucci, S; Capon, F; Nistico', Sp; Chimenti, S; Pallone, F; Novelli, G
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3
2000-01-01 Sangiuolo, Fc; Bruscia, E; Capon, F; Servidei, S; Dallapiccola, B; Novelli, G
Insight into genetics of atopic dermatitis: future approaches and directions
2003-01-01 Novelli, G; Giardina, E; Paradisi, M; Pedicelli, C; Girolomoni, G; Nasorri, F; Chimenti, S; Marulli, G; Rossi, P; Moschese, V; Chini, L; Capon, F
Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26
2001-01-01 Mangino, M; Flex, E; Capon, F; Sangiuolo, Fc; Carraro, E; Gualandi, F; Mazzoli, M; Martini, A; Novelli, G; Dallapiccola, B
Molecular prenatal diagnosis of neuromuscular disorders
1997-01-01 Dallapiccola, B; Capon, F; Gennarelli, M; Torrente, I; Mingarelli, R; Novelli, G
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre
2002-01-01 Giardina, E; Capon, F; D'Apice, Mr; Amati, F; Arturi, A; Filetti, S; Bonifazi, E; Pucci, S; Conte, C; Novelli, G
The long and winding road: Searching for non-MHC psoriasis susceptibility loci
2005-01-01 Capon, F; Giardina, E
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
11-set-1999 | A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13 | Servidei, S; Capon, F; Spinazzola, A; Mirabella, M; Semprini, S; de Rosa, G; Gennarelli, M; Sangiuolo, Fc; Ricci, E; Mohrenweiser, H; Dallapiccola, B; Tonali, P; 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-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-2000 | Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3 | Sangiuolo, Fc; Bruscia, E; Capon, F; Servidei, S; Dallapiccola, B; Novelli, G | 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-2001 | Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26 | Mangino, M; Flex, E; Capon, F; Sangiuolo, Fc; Carraro, E; Gualandi, F; Mazzoli, M; Martini, A; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-gen-1997 | Molecular prenatal diagnosis of neuromuscular disorders | Dallapiccola, B; Capon, F; Gennarelli, M; Torrente, I; Mingarelli, R; Novelli, G | Contributo in libro | |
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-2005 | The long and winding road: Searching for non-MHC psoriasis susceptibility loci | Capon, F; Giardina, E | Articolo su rivista |