CASTALDO, GIUSEPPE
CASTALDO, GIUSEPPE
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
The Italian database of haemophilia B mutations
2003 Tagariello, G; Belvini, D; Salviato, R; Radossi, P; Mori, Pg; Castaldo, Giuseppe; And, Aice
Complex Multigenic Inheritance Influences the Development of Severe CF Liver Disease in CF.
2000 Friedman, Kj; Ling, Sc; MACEK M., Jr; Handler, Aj; Zhou, Z; Pace, Rg; Mack, Dr; Colombo, Jl; Vvrov, V; Castaldo, Giuseppe; Spina, M; Salvatore, F; Phillips, Mj; Zielenski, J; Tsui, Lc; Durie, Pr; Silverman, Lm; Knowles, M. R.
Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants.
2008 Daniele, A.; Cardillo, Giuseppe; Pennino, C.; Carbone, M. T.; Scognamiglio, Diego; Esposito, L.; Correra, A.; Castaldo, Giuseppe; Zagari, Adriana; Salvatore, Francesco
A Novel Promising Therapeutic Option Against Hepatitis C Virus: An Oral Nucleotide NS5B Polymerase Inhibitor Sofosbuvir
2013 Gentile, Ivan; F., Borgia; Buonomo, ANTONIO RICCARDO; Castaldo, Giuseppe; Borgia, Guglielmo
Brand new SPINK1 and CFTR mutations in a child with acute recurrent pancreatitis: a case report.
2013 Terlizzi, Vito; DE GREGORIO, Fabiola; Sepe, A; Amato, N; Arduino, C; Casale, A; Majo, Fabio; Tomaiuolo, Rossella; Castaldo, Giuseppe; Raia, Valeria
Identification and role of the hemostasis and thrombosis expert in the National Health System
2014 Rodeghiero, F; Morfini, M; Nozzoli, C; Manotti, C; Violi, F; Castaldo, Giuseppe; Pane, Fabrizio; Biasioli, B; Velati, C.
Genetic modifiers of liver disease in cystic fibrosis.
2009 Bartlett, Jr; Friedman, Kj; Ling, Sc; Pace, Rg; Bell, Sc; Bourke, B; Castaldo, Giuseppe; Castellani, C; Cipolli, M; Colombo, C; Colombo, Jl; Debray, D; Fernandez, A; Lacaille, F; Macek M., Jr; Rowland, M; Salvatore, Francesco; Taylor, Cj; Wainwright, C; Wilschanski, M; Zemková, D; Hannah, Wb; Phillips, Mj; Corey, M; Zielenski, J; Dorfman, R; Wang, Y; Zou, F; Silverman, Lm; Drumm, Ml; Wright, Fa; Lange, Em; Durie, Pr; Knowles, Mr; Collaborators: Clancy JP, Gene Modifier Study G. r. o. u. p.; Sindel, Lj; Roberts, Dm; Roberts, V; Radford, Pj; Argel, N; Morgan, Wj; Douthit, Jl; Schellhase, De; Anderson, P; Taggart, A; Morrissey, B; Platzker, Ac; Woo, Ms; Fukushima, L; Hsu, E; Shay, Gf; Hardy, Ka; Moss, Rb; Dunn, Ce; Pian, Ms; Wojtczak, Ha; Burns, L; Henig, Nr; Nielson, Dw; Landon, C; Thompson, A; Accurso, Fj; Nick, Ja; Jones, M; Lapin, C; Drapeau, Vm; Egan, Me; Padman, R; Winnie, Gb; George, C; Olson, El; Light, Mj; Geller, De; Gondor, M; Flanary, J; Stecenko, Aa; Guill, Mf; Mccolley, Sa; Mccolley, Sa; Potter, Em; Chung, Y; Garvey, M; Howenstine, Ms; Sannuti, A; Yeley, J; Sloven, Dg; Ahrens, Rc; Teresi, M; Riva, Cm; Davis, S; Quiniones Ellis, B; Gabor, C; Lever, Tf; Welch, R; Cairns, A; Corrigan, M; Zeitlin, Pl; Brass, L; Dorkin, H; Levy, H; Huntington, I; O'Sullivan, Bp; Simon, Rh; Nasr, Sz; Lumeng, N; Ball, Me; Toder, Ds; Honicky, Re; Fitch, S; Contreras, L; Regelmann, We; Phillips, Jr; Mcnamara, J; Johnson, M; Ruiz, Fe; Adcock, Kg; Konig, P; Black, P; Weigel, Jd; Noyes, Be; Kociela, Vl; Ferkol T., Jr; Boyle, M; Colombo, Jl; Brascia, T; Parker, Hw; Zanni, Rl; Fiel, Sb; Lomas, P; Taylor Cousar, J; Borowitz, D; DeCelie Germana, Jk; Cohen, R; Gannon, M; Dimango, Ea; Mencin, Aa; Lobritto, Sj; Benitez, M; Walker, Pa; Berdella, Mn; Langfelder Schwind, E; Ren, Cl; Rovitelli, Ak; Anbar, Rd; Lindner, Dm; Perciaccante, Rg; Dozor, Aj; Knowles, Mr; Leigh, Mw; Taylor Cousar, J; Voynow, Ja; Auten, Kj; Schechter, Ms; Omlor, Gj; Ouellette, Da; Karp, Cl; Joseph, Pm; Konstan, Mw; Mccoy, Ks; Royce, F; Bartosik, S; Vauthy, Pa; Vauthy, Ml; Kramer, Jc; Hensel, S; Perez, Cr; Thomas, Nj; Hess, Jc; Holsclaw, Ds; Scanlin, Tf; Rubenstein, R; Murray, C; Skotleski, M; Fiel, Sb; Sexauer, Wp; Ko, A; Hillman, J; Orenstein, Dm; Schechter, Ms; Flume, Pa; Brown, D; Schoumacher, R; Culbreath, B; Moore, Pe; Slovis, B; Dambro, N; Garbarz, J; Hiatt, Pw; Olivier, Kn; Amaro, R; Macleod, L; Liou, Tg; Froh, Dk; Epstein, Ce; Schmidt, J; Elliot, G; Williams, R; Anderson, M; Gadd, J; Gibson, Rl; Mcnamara, S; Worrell, K; Moskowitz, Sm; Mccarthy, M; Llewellyn, C; Wicks, S; Moffett, Ks; Baer, Ls; do Pico, Ga; Makholm, Lm; Rock, Mj; Osmond, Sr; Biller, J; Miller, T; Fernandez, A; Renteria, F; Bell, Sc; Wainwright, C; Lewindon, P; Selvadurai, H; Gaskin, K; Van Biervliet, S; Montgomery, M; Rabin, Hr; Leong, J; Zuberbuhler, P; Brown, Ne; Tabak, J; Davidson, Ag; Nakielna, Em; Habbick, B; Waters, I; Wiltse, S; Kepron, W; Pasterkamp, H; Garey, Dn; Bishop, G; Noseworthy, M; Michael, Rt; Dale, Am; Gosse, Fa; Robinson, W; Durie, Pr; Corey, M; Freitag, A; Pedder, L; Van Wylick, R; Lougheed, Md; Kodiattu, L; Jackson, M; Malhotra, K; Lyttle, B; Paterson, Na; Aaron, S; Boland, M; Kovesi, T; Smith, A; Kumar, Vj; Zinger, S; Tullis, E; Simard, F; Rivard, L; Cantin, A; Cote, G; Lands, Lc; Marcotte, Je; Matouk, E; Berthiaume, Y; Jeanneret, A; Van Spall, M; Rivard, G; Boucher, J; Petit, N; Holmes, B; Cotton, D; Ramlall, K; Repetto, G; Macek M., Jr; Vavrova, V; Bartosova, J; Fila, L; Debray, D; Lacaille, F; Munck, A; Tümmler, B; Rowland, M; Bourke, B; Canny, G; Gallagher, C; Rivlin, J; Picard, E; Blau, H; Wilschanski, M; Springer, C; Kerem, E; Yahav, Y; Bujanover, Y; Casciaro, R; Colombo, C; Castaldo, G; Salvatore, F; Raia, Valeria; Cipolli, M; Castellani, C; Sinaasappel, M; Dooijes, D; Ling, Sc; Kayserova, H; Ozcelik, U; Kiper, N; Dogru, D; Taylor, Cj; Mcgaw, J.
Prenatal diagnosis of inherited diseases: 20 years? experience of an Italian Regional Reference Centre
2013 Maruotti, GIUSEPPE MARIA; Frisso, Giulia; G., Calcagno; Fortunato, Giuliana; Castaldo, Giuseppe; Martinelli, Pasquale; Sacchetti, Lucia; Salvatore, Francesco
Efficacy and Safety of Sofosbuvir in Treatment of Chronic Hepatitis C: The Dawn of the a New Era.
2014 Gentile, Ivan; F., Borgia; E., Zappulo; Buonomo, ANTONIO RICCARDO; A. M., Spera; Castaldo, Giuseppe; Borgia, Guglielmo
Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management
2010 BERNI CANANI, Roberto; Cardillo, Giuseppe; Terrin, Gianluca; Castaldo, Giuseppe
Recurrent pregnancy loss and thrombophilia.
2007 DI MICCO, P; D'Uva, Maristella; Strina, Ida; DE PLACIDO, Giuseppe; DI FIORE, Rosanna; Quaranta, Sandro; Castaldo, Giuseppe
Carcinoembryonic antigen mRNA analysis detects micrometsatatic cells in blood from lung cancer patients.
2003 Castaldo, Giuseppe; Tomaiuolo, Rossella; Sanduzzi, A; Ponticiello, Antonio; Marchetiello, I; Salvatore, Francesco
Sequence analysis revealed a high frequency of CFTR mutations in patients bearing atypical forms of Cystic Fibrosis.
2001 Spina, M; Cardillo, G; Castaldo, Giuseppe; Salvatore, F.
Analysis of polymorphisms in the human beta-defensin 1 and 2 genes.
2001 Vankeerberghen, Al; Scudiero, Olga; DE BOECK, K; Castaldo, Giuseppe; Cuppens, H; Salvatore, F; Cassiman, J. J.
A novel denaturing-HPLC (D-HPLC) procedure for the screening of PAH gene in phenylketonuria.
2003 Daniele, A; Cardillo, G; Pennino, C; Scognamiglio, D; Pignero, A; Castaldo, Giuseppe; Salvatore, F.
Molecular diagnosis of Cystic Fibrosis: comparison of four analytical procedures
2003 Tomaiuolo, Rossella; Spina, M. C.; Castaldo, Giuseppe
Diagnosi prenatale della sindrome nude-SCID.
2009 Calcagno, G; Ursini, Mv; Castaldo, Giuseppe; Fusco, Anna; Martinelli, Pasquale; Pignata, Claudio; Salvatore, Francesco
Epistasis in cystic fibrosis.
2006 Salvatore, Francesco; Castaldo, Giuseppe
A Large Cluster Headache family suggestive of autosomal recessive inheritance
2003 DE SIMONE, Roberto; Fiorillo, Chiara; Bonuso, Salvatore; Castaldo, Giuseppe
La farmacogenetica nella terapia anticoagulante orale:dall’analisi genetica alla pratica clinica
2010 Mazzaccara, Cristina; Toriello, Mario; Liguori, R; Tomaiuolo, Rossella; Cottarelli, A; Vitale, D. F.; Meccariello, Pasquale; Castaldo, Giuseppe; Sacchetti, Lucia
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| The Italian database of haemophilia B mutations | 4.1 Articoli in Atti di convegno | 2003 | Tagariello, G; Belvini, D; Salviato, R; Radossi, P; Mori, Pg; Castaldo, Giuseppe; And, Aice | |
| Complex Multigenic Inheritance Influences the Development of Severe CF Liver Disease in CF. | 4.1 Articoli in Atti di convegno | 2000 | Friedman, Kj; Ling, Sc; MACEK M., Jr; Handler, Aj; Zhou, Z; Pace, Rg; Mack, Dr; Colombo, Jl; Vvrov, V; Castaldo, Giuseppe; Spina, M; Salvatore, F; Phillips, Mj; Zielenski, J; Tsui, Lc; Durie, Pr; Silverman, Lm; Knowles, M. R. | |
| Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants. | 1.1 Articolo in rivista | 2008 | Daniele, A.; Cardillo, Giuseppe; Pennino, C.; Carbone, M. T.; Scognamiglio, Diego; Esposito, L.; Correra, A.; Castaldo, Giuseppe; Zagari, Adriana; Salvatore, Francesco | |
| A Novel Promising Therapeutic Option Against Hepatitis C Virus: An Oral Nucleotide NS5B Polymerase Inhibitor Sofosbuvir | 1.1 Articolo in rivista | 2013 | Gentile, Ivan; F., Borgia; Buonomo, ANTONIO RICCARDO; Castaldo, Giuseppe; Borgia, Guglielmo | |
| Brand new SPINK1 and CFTR mutations in a child with acute recurrent pancreatitis: a case report. | 1.1 Articolo in rivista | 2013 | Terlizzi, Vito; DE GREGORIO, Fabiola; Sepe, A; Amato, N; Arduino, C; Casale, A; Majo, Fabio; Tomaiuolo, Rossella; Castaldo, Giuseppe; Raia, Valeria | |
| Identification and role of the hemostasis and thrombosis expert in the National Health System | 1.1 Articolo in rivista | 2014 | Rodeghiero, F; Morfini, M; Nozzoli, C; Manotti, C; Violi, F; Castaldo, Giuseppe; Pane, Fabrizio; Biasioli, B; Velati, C. | |
| Genetic modifiers of liver disease in cystic fibrosis. | 1.1 Articolo in rivista | 2009 | Bartlett, Jr; Friedman, Kj; Ling, Sc; Pace, Rg; Bell, Sc; Bourke, B; Castaldo, Giuseppe; Castellani, C; Cipolli, M; Colombo, C; Colombo, Jl; Debray, D; Fernandez, A; Lacaille, F; Macek M., Jr; Rowland, M; Salvatore, Francesco; Taylor, Cj; Wainwright, C; Wilschanski, M; Zemková, D; Hannah, Wb; Phillips, Mj; Corey, M; Zielenski, J; Dorfman, R; Wang, Y; Zou, F; Silverman, Lm; Drumm, Ml; Wright, Fa; Lange, Em; Durie, Pr; Knowles, Mr; Collaborators: Clancy JP, Gene Modifier Study G. r. o. u. p.; Sindel, Lj; Roberts, Dm; Roberts, V; Radford, Pj; Argel, N; Morgan, Wj; Douthit, Jl; Schellhase, De; Anderson, P; Taggart, A; Morrissey, B; Platzker, Ac; Woo, Ms; Fukushima, L; Hsu, E; Shay, Gf; Hardy, Ka; Moss, Rb; Dunn, Ce; Pian, Ms; Wojtczak, Ha; Burns, L; Henig, Nr; Nielson, Dw; Landon, C; Thompson, A; Accurso, Fj; Nick, Ja; Jones, M; Lapin, C; Drapeau, Vm; Egan, Me; Padman, R; Winnie, Gb; George, C; Olson, El; Light, Mj; Geller, De; Gondor, M; Flanary, J; Stecenko, Aa; Guill, Mf; Mccolley, Sa; Mccolley, Sa; Potter, Em; Chung, Y; Garvey, M; Howenstine, Ms; Sannuti, A; Yeley, J; Sloven, Dg; Ahrens, Rc; Teresi, M; Riva, Cm; Davis, S; Quiniones Ellis, B; Gabor, C; Lever, Tf; Welch, R; Cairns, A; Corrigan, M; Zeitlin, Pl; Brass, L; Dorkin, H; Levy, H; Huntington, I; O'Sullivan, Bp; Simon, Rh; Nasr, Sz; Lumeng, N; Ball, Me; Toder, Ds; Honicky, Re; Fitch, S; Contreras, L; Regelmann, We; Phillips, Jr; Mcnamara, J; Johnson, M; Ruiz, Fe; Adcock, Kg; Konig, P; Black, P; Weigel, Jd; Noyes, Be; Kociela, Vl; Ferkol T., Jr; Boyle, M; Colombo, Jl; Brascia, T; Parker, Hw; Zanni, Rl; Fiel, Sb; Lomas, P; Taylor Cousar, J; Borowitz, D; DeCelie Germana, Jk; Cohen, R; Gannon, M; Dimango, Ea; Mencin, Aa; Lobritto, Sj; Benitez, M; Walker, Pa; Berdella, Mn; Langfelder Schwind, E; Ren, Cl; Rovitelli, Ak; Anbar, Rd; Lindner, Dm; Perciaccante, Rg; Dozor, Aj; Knowles, Mr; Leigh, Mw; Taylor Cousar, J; Voynow, Ja; Auten, Kj; Schechter, Ms; Omlor, Gj; Ouellette, Da; Karp, Cl; Joseph, Pm; Konstan, Mw; Mccoy, Ks; Royce, F; Bartosik, S; Vauthy, Pa; Vauthy, Ml; Kramer, Jc; Hensel, S; Perez, Cr; Thomas, Nj; Hess, Jc; Holsclaw, Ds; Scanlin, Tf; Rubenstein, R; Murray, C; Skotleski, M; Fiel, Sb; Sexauer, Wp; Ko, A; Hillman, J; Orenstein, Dm; Schechter, Ms; Flume, Pa; Brown, D; Schoumacher, R; Culbreath, B; Moore, Pe; Slovis, B; Dambro, N; Garbarz, J; Hiatt, Pw; Olivier, Kn; Amaro, R; Macleod, L; Liou, Tg; Froh, Dk; Epstein, Ce; Schmidt, J; Elliot, G; Williams, R; Anderson, M; Gadd, J; Gibson, Rl; Mcnamara, S; Worrell, K; Moskowitz, Sm; Mccarthy, M; Llewellyn, C; Wicks, S; Moffett, Ks; Baer, Ls; do Pico, Ga; Makholm, Lm; Rock, Mj; Osmond, Sr; Biller, J; Miller, T; Fernandez, A; Renteria, F; Bell, Sc; Wainwright, C; Lewindon, P; Selvadurai, H; Gaskin, K; Van Biervliet, S; Montgomery, M; Rabin, Hr; Leong, J; Zuberbuhler, P; Brown, Ne; Tabak, J; Davidson, Ag; Nakielna, Em; Habbick, B; Waters, I; Wiltse, S; Kepron, W; Pasterkamp, H; Garey, Dn; Bishop, G; Noseworthy, M; Michael, Rt; Dale, Am; Gosse, Fa; Robinson, W; Durie, Pr; Corey, M; Freitag, A; Pedder, L; Van Wylick, R; Lougheed, Md; Kodiattu, L; Jackson, M; Malhotra, K; Lyttle, B; Paterson, Na; Aaron, S; Boland, M; Kovesi, T; Smith, A; Kumar, Vj; Zinger, S; Tullis, E; Simard, F; Rivard, L; Cantin, A; Cote, G; Lands, Lc; Marcotte, Je; Matouk, E; Berthiaume, Y; Jeanneret, A; Van Spall, M; Rivard, G; Boucher, J; Petit, N; Holmes, B; Cotton, D; Ramlall, K; Repetto, G; Macek M., Jr; Vavrova, V; Bartosova, J; Fila, L; Debray, D; Lacaille, F; Munck, A; Tümmler, B; Rowland, M; Bourke, B; Canny, G; Gallagher, C; Rivlin, J; Picard, E; Blau, H; Wilschanski, M; Springer, C; Kerem, E; Yahav, Y; Bujanover, Y; Casciaro, R; Colombo, C; Castaldo, G; Salvatore, F; Raia, Valeria; Cipolli, M; Castellani, C; Sinaasappel, M; Dooijes, D; Ling, Sc; Kayserova, H; Ozcelik, U; Kiper, N; Dogru, D; Taylor, Cj; Mcgaw, J. | |
| Prenatal diagnosis of inherited diseases: 20 years? experience of an Italian Regional Reference Centre | 1.1 Articolo in rivista | 2013 | Maruotti, GIUSEPPE MARIA; Frisso, Giulia; G., Calcagno; Fortunato, Giuliana; Castaldo, Giuseppe; Martinelli, Pasquale; Sacchetti, Lucia; Salvatore, Francesco | |
| Efficacy and Safety of Sofosbuvir in Treatment of Chronic Hepatitis C: The Dawn of the a New Era. | 1.1 Articolo in rivista | 2014 | Gentile, Ivan; F., Borgia; E., Zappulo; Buonomo, ANTONIO RICCARDO; A. M., Spera; Castaldo, Giuseppe; Borgia, Guglielmo | |
| Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management | 1.1 Articolo in rivista | 2010 | BERNI CANANI, Roberto; Cardillo, Giuseppe; Terrin, Gianluca; Castaldo, Giuseppe | |
| Recurrent pregnancy loss and thrombophilia. | 1.1 Articolo in rivista | 2007 | DI MICCO, P; D'Uva, Maristella; Strina, Ida; DE PLACIDO, Giuseppe; DI FIORE, Rosanna; Quaranta, Sandro; Castaldo, Giuseppe | |
| Carcinoembryonic antigen mRNA analysis detects micrometsatatic cells in blood from lung cancer patients. | 1.1 Articolo in rivista | 2003 | Castaldo, Giuseppe; Tomaiuolo, Rossella; Sanduzzi, A; Ponticiello, Antonio; Marchetiello, I; Salvatore, Francesco | |
| Sequence analysis revealed a high frequency of CFTR mutations in patients bearing atypical forms of Cystic Fibrosis. | 4.1 Articoli in Atti di convegno | 2001 | Spina, M; Cardillo, G; Castaldo, Giuseppe; Salvatore, F. | |
| Analysis of polymorphisms in the human beta-defensin 1 and 2 genes. | 4.1 Articoli in Atti di convegno | 2001 | Vankeerberghen, Al; Scudiero, Olga; DE BOECK, K; Castaldo, Giuseppe; Cuppens, H; Salvatore, F; Cassiman, J. J. | |
| A novel denaturing-HPLC (D-HPLC) procedure for the screening of PAH gene in phenylketonuria. | 4.1 Articoli in Atti di convegno | 2003 | Daniele, A; Cardillo, G; Pennino, C; Scognamiglio, D; Pignero, A; Castaldo, Giuseppe; Salvatore, F. | |
| Molecular diagnosis of Cystic Fibrosis: comparison of four analytical procedures | 1.1 Articolo in rivista | 2003 | Tomaiuolo, Rossella; Spina, M. C.; Castaldo, Giuseppe | |
| Diagnosi prenatale della sindrome nude-SCID. | 8.02 Comunicazioni a Convegni o Seminari | 2009 | Calcagno, G; Ursini, Mv; Castaldo, Giuseppe; Fusco, Anna; Martinelli, Pasquale; Pignata, Claudio; Salvatore, Francesco | |
| Epistasis in cystic fibrosis. | 2.1 Contributo in volume (Capitolo o Saggio) | 2006 | Salvatore, Francesco; Castaldo, Giuseppe | |
| A Large Cluster Headache family suggestive of autosomal recessive inheritance | 1.1 Articolo in rivista | 2003 | DE SIMONE, Roberto; Fiorillo, Chiara; Bonuso, Salvatore; Castaldo, Giuseppe | |
| La farmacogenetica nella terapia anticoagulante orale:dall’analisi genetica alla pratica clinica | 4.2 Abstract in Atti di convegno | 2010 | Mazzaccara, Cristina; Toriello, Mario; Liguori, R; Tomaiuolo, Rossella; Cottarelli, A; Vitale, D. F.; Meccariello, Pasquale; Castaldo, Giuseppe; Sacchetti, Lucia |