Sfoglia per Autore
Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome.
2006-01-01 Bachetti T; Robbiano Angela; Parodi S; Matera I; Merello E; Capra V; Baglietto MP; Rossi A; Ceccherini I; Ottonello G.
Clinical and genetic study of primary hyperoxaluria in Italy
2008-01-01 Robbiano A ; Mandrile G ; Giachino D ; Petrarulo M ; Pirulli D ; Zadro C ; Marangella M ; Amoroso A ; Peruzzi L ; Murer L ; Picca S ; De Marchi M
The Italian Multicenter Study of Primary Hyperoxaluria
2008-01-01 Licia Peruzzi; Angela Robbiano; Giorgia Mandrile; Daniela Giachino; Michele Petrarulo; Martino Marangella; Rosanna Coppo; Luisa Murer; Stefano Picca; Sonia Berardi; Giovanni Mosconi; Antonio Amoroso; Mario De Marchi
Primary hyperoxaluria in Italy
2008-01-01 Robbiano, Angela; Mandrile, Giorgia; Petrarulo, M.; Pirulli, D.; Zadro, C.; Giachino, Daniela Francesca; Marangella, M.; Amoroso, Antonio; DE MARCHI, Mario
Differential regulation of interleukin 12 and interleukin 23 production in human dendritic cells
2008-01-01 Franca Gerosa; Barbara Baldani-Guerra; Lyudmila A Lyakh; Giovanna Batoni; Semih Esin; Robin T Winkler-Pickett; Maria Rita Consolaro; Mario De Marchi; Daniela Giachino; Angela Robbiano; Marco Astegiano; Angela Sambataro; Robert A Kastelein; Giuseppe Carra; Giorgio Trinchieri
Primary hyperoxaluria: report of an Italian family with clear sex conditioned penetrance
2008-01-01 Mandrile G; Robbiano A; Giachino DF; Sebastiano R; Dondi E; Fenoglio R; Stratta P; Caruso MR; Petrarulo M; Marangella M; De Marchi M.
Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene
2009-01-01 Williams EL; Acquaviva C; Amoroso A; Chevalier F; Coulter-Mackie M; Monico CG; Giachino D; Owen T; Robbiano A; Salido E; Waterham H; Rumsby G
Novel human pathological mutations. Gene symbol: AGXT. Disease: hyperoxaluria
2010-01-01 Robbiano A; Mandrile G; De Marchi M; Beck B; Baasner A; Murer L; Benetti E; Giachino D.
Modeling the effect of 3 missense AGXT mutations on dimerization of the AGT enzyme in primary hyperoxaluria type I
2010-01-01 Robbiano A.; Frecer V.; Miertus J.; Zadro C.; Ulivi S.; Bevilacqua E.; Mandrile G.; De Marchi M.; Miertus S.; Amoroso A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome. | 2006 | Bachetti T; Robbiano Angela; Parodi S; Matera I; Merello E; Capra V; Baglietto MP; Rossi A; Ceccherini I; Ottonello G. | |
| Clinical and genetic study of primary hyperoxaluria in Italy | 2008 | Robbiano A ; Mandrile G ; Giachino D ; Petrarulo M ; Pirulli D ; Zadro C ; Marangella M ; Amoroso A ; Peruzzi L ; Murer L ; Picca S ; De Marchi M | |
| The Italian Multicenter Study of Primary Hyperoxaluria | 2008 | Licia Peruzzi; Angela Robbiano; Giorgia Mandrile; Daniela Giachino; Michele Petrarulo; Martino Marangella; Rosanna Coppo; Luisa Murer; Stefano Picca; Sonia Berardi; Giovanni Mosconi; Antonio Amoroso; Mario De Marchi | |
| Primary hyperoxaluria in Italy | 2008 | Robbiano, Angela; Mandrile, Giorgia; Petrarulo, M.; Pirulli, D.; Zadro, C.; Giachino, Daniela Francesca; Marangella, M.; Amoroso, Antonio; DE MARCHI, Mario | |
| Differential regulation of interleukin 12 and interleukin 23 production in human dendritic cells | 2008 | Franca Gerosa; Barbara Baldani-Guerra; Lyudmila A Lyakh; Giovanna Batoni; Semih Esin; Robin T Winkler-Pickett; Maria Rita Consolaro; Mario De Marchi; Daniela Giachino; Angela Robbiano; Marco Astegiano; Angela Sambataro; Robert A Kastelein; Giuseppe Carra; Giorgio Trinchieri | |
| Primary hyperoxaluria: report of an Italian family with clear sex conditioned penetrance | 2008 | Mandrile G; Robbiano A; Giachino DF; Sebastiano R; Dondi E; Fenoglio R; Stratta P; Caruso MR; Petrarulo M; Marangella M; De Marchi M. | |
| Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene | 2009 | Williams EL; Acquaviva C; Amoroso A; Chevalier F; Coulter-Mackie M; Monico CG; Giachino D; Owen T; Robbiano A; Salido E; Waterham H; Rumsby G | |
| Novel human pathological mutations. Gene symbol: AGXT. Disease: hyperoxaluria | 2010 | Robbiano A; Mandrile G; De Marchi M; Beck B; Baasner A; Murer L; Benetti E; Giachino D. | |
| Modeling the effect of 3 missense AGXT mutations on dimerization of the AGT enzyme in primary hyperoxaluria type I | 2010 | Robbiano A.; Frecer V.; Miertus J.; Zadro C.; Ulivi S.; Bevilacqua E.; Mandrile G.; De Marchi M.; Miertus S.; Amoroso A. |
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