Sfoglia per Titolo
Genetic Factors Associated with Age-Related Macular Degeneration
2011-01-01 Leveziel, N; Tilleul, J; Puche, N; Zerbib, J; Laloum, F; Querques, Giuseppe; Souied, Eh
Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project
2013-01-01 Cleynen, I; Gonzalez, Jr; Figueroa, C; Franke, A; Mcgovern, D; Bortlik, M; Crusius, Bja; Vecchi, M; Artieda, M; Szczypiorska, M; Bethge, J; Arteta, D; Ayala, E; Danese, S; van Hogezand, Ra; Panes, J; Pena, Sa; Lukas, M; Jewell, Dp; Schreiber, S; Vermeire, S; Sans, M
Genetic factors predicting executive functioning in healthy subjects and obsessive compulsive spectrum disorder patients
2006-01-01 Cavallini, Mc; Cavedini, P; Zorzi, C; Piccinni, M; Stazi, A; Bellodi, Laura
Genetic factors predisposing to bronchopulmonary dysplasia. A pilot study by exome sequencing and pathways analysis
2015-01-01 Somaschini, M; DI RESTA, Chiara; Volonteri, C; Castiglioni, E; Bonfiglios, ; Lazarevic, D; Cittaro, D; Stupka, E; Ferrari, Maurizio; Carrera, P; Bpd, ; Genetics Study, Group
The Genetic Germline Background of Single and Multiple Primary Melanomas
2021-01-01 De Summa, S.; Lasorella, A.; Strippoli, S.; Giudice, G.; Guida, G.; Elia, R.; Nacchiero, E.; Azzariti, A.; Silvestris, N.; Guida, M.; Guida, S.; Tommasi, S.; Pinto, R.
Genetic heterogeneity in atrial septal defects
1997-01-01 Chessa, M; Aggoun, Y; Bonhoeffer, P
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)
1998-01-01 Gambardella, A; Bolino, A; Muglia, M; Valentino, P; Bono, F; Oliveri, Rl; Sabatelli, M; Brancolini, V; Van Broeckhoven, C; Romeo, G; Devoto, M; Quattrone, A
Genetic heterogeneity in interatrial defect
1997-01-01 Chessa, M.; Aggoun, Y.; Bonhoeffer, P.; Butera, G.; Lyonnet, S.; Bonnet, D.
Genetic heterogeneity in Malattia Leventinese
2002-01-01 Toto, L; Parodi, Mb; Barelle, F; Casari, GIORGIO NEVIO; Ravalico, G; Romano, M.
Genetic heterogeneity in Malattia Leventinese (vol 62, pg 399, 2002)
2004-01-01 Toto, L; Parodi, Mb; Baralle, F; Casari, GIORGIO NEVIO; Ravalico, G; Romano, M.
Genetic Heterogenity in Italian Families with Familial Hemiplegic Migraine
1999-01-01 Carrera, P.; Piatti, M.; Stenirri, S.; Grimaldi, L. M. E.; Marchioni, E.; Curcio, M.; Righetti, Pg; Ferrari, Maurizio; Gelfi, C.
Genetic history of PKU mutations in Italy
1994-01-01 Dianzani, I; Giannattasio, S; De Sanctis, L; Marra, E; Ponzone, A; Camaschella, Clara; Piazza, A.
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3)
2002-01-01 Cazzola, M; Cremonesi, L; Papaioannou, M; Soriani, N; Kioumi, A; Charalambidou, A; Paroni, R; Romtsou, K; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Christakis, J.
Genetic hypertension and kidney
1984-01-01 Bianchi, G; Ferrari, P; Cusi, D; Guidi, E; Pati, C; Vezzoli, G; Tripodi, G; Niutta, E
Genetic impact on renal function decay in radical and partial nephrectomy
2012-01-01 Sciarrone Alibrandi, Mt; Trevisani, F; Delli Carpini, S; Simonini, M; Camerota, T; Merlino, L; Zagato, L; Brioni, E; Bertini, R; Montorsi, Francesco; Rigatti, P; Manunta, Paolo
Genetic influence of adducing genes on ischemic strokes.
2013-01-01 Merlino, L; Giacalone, G; Zagato, L; Rainone, F; Sessa, M; Casamassima, N; Simonini, M; Comi, G; Manunta, Paolo
Genetic influence on response to serotonergic antidepressants.
2000-01-01 Zanardi, R; Benedetti, F; Serretti, A; Smeraldi, E
Genetic Interaction between MTMR2 and FIG4 Phospholipid Phosphatases Involved in Charcot-Marie-Tooth Neuropathies
2011-01-01 Vaccari, I; Dina, G; Tronchere, H; Kaufman, E; Chicanne, G; Cerri, F; Wrabetz, L; Payrastre, B; Quattrini, A; Weisman, Ls; Meisler, Mh; Bolino, A
Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration
2009-01-01 Martinelli, P; La Mattina, V; Bernacchia, A; Magnoni, R; Cerri, F; Cox, G; Quattrini, A; Casari, GIORGIO NEVIO; Rugarli, Ei
The Genetic Makeup of Myeloproliferative Neoplasms: Role of Germline Variants in Defining Disease Risk, Phenotypic Diversity and Outcome
2021-01-01 Masselli, Elena; Pozzi, Giulia; Carubbi, Cecilia; Vitale, Marco.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Genetic Factors Associated with Age-Related Macular Degeneration | 1-gen-2011 | Leveziel, N; Tilleul, J; Puche, N; Zerbib, J; Laloum, F; Querques, Giuseppe; Souied, Eh | |
Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project | 1-gen-2013 | Cleynen, I; Gonzalez, Jr; Figueroa, C; Franke, A; Mcgovern, D; Bortlik, M; Crusius, Bja; Vecchi, M; Artieda, M; Szczypiorska, M; Bethge, J; Arteta, D; Ayala, E; Danese, S; van Hogezand, Ra; Panes, J; Pena, Sa; Lukas, M; Jewell, Dp; Schreiber, S; Vermeire, S; Sans, M | |
Genetic factors predicting executive functioning in healthy subjects and obsessive compulsive spectrum disorder patients | 1-gen-2006 | Cavallini, Mc; Cavedini, P; Zorzi, C; Piccinni, M; Stazi, A; Bellodi, Laura | |
Genetic factors predisposing to bronchopulmonary dysplasia. A pilot study by exome sequencing and pathways analysis | 1-gen-2015 | Somaschini, M; DI RESTA, Chiara; Volonteri, C; Castiglioni, E; Bonfiglios, ; Lazarevic, D; Cittaro, D; Stupka, E; Ferrari, Maurizio; Carrera, P; Bpd, ; Genetics Study, Group | |
The Genetic Germline Background of Single and Multiple Primary Melanomas | 1-gen-2021 | De Summa, S.; Lasorella, A.; Strippoli, S.; Giudice, G.; Guida, G.; Elia, R.; Nacchiero, E.; Azzariti, A.; Silvestris, N.; Guida, M.; Guida, S.; Tommasi, S.; Pinto, R. | |
Genetic heterogeneity in atrial septal defects | 1-gen-1997 | Chessa, M; Aggoun, Y; Bonhoeffer, P | |
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B) | 1-gen-1998 | Gambardella, A; Bolino, A; Muglia, M; Valentino, P; Bono, F; Oliveri, Rl; Sabatelli, M; Brancolini, V; Van Broeckhoven, C; Romeo, G; Devoto, M; Quattrone, A | |
Genetic heterogeneity in interatrial defect | 1-gen-1997 | Chessa, M.; Aggoun, Y.; Bonhoeffer, P.; Butera, G.; Lyonnet, S.; Bonnet, D. | |
Genetic heterogeneity in Malattia Leventinese | 1-gen-2002 | Toto, L; Parodi, Mb; Barelle, F; Casari, GIORGIO NEVIO; Ravalico, G; Romano, M. | |
Genetic heterogeneity in Malattia Leventinese (vol 62, pg 399, 2002) | 1-gen-2004 | Toto, L; Parodi, Mb; Baralle, F; Casari, GIORGIO NEVIO; Ravalico, G; Romano, M. | |
Genetic Heterogenity in Italian Families with Familial Hemiplegic Migraine | 1-gen-1999 | Carrera, P.; Piatti, M.; Stenirri, S.; Grimaldi, L. M. E.; Marchioni, E.; Curcio, M.; Righetti, Pg; Ferrari, Maurizio; Gelfi, C. | |
Genetic history of PKU mutations in Italy | 1-gen-1994 | Dianzani, I; Giannattasio, S; De Sanctis, L; Marra, E; Ponzone, A; Camaschella, Clara; Piazza, A. | |
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3) | 1-gen-2002 | Cazzola, M; Cremonesi, L; Papaioannou, M; Soriani, N; Kioumi, A; Charalambidou, A; Paroni, R; Romtsou, K; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Christakis, J. | |
Genetic hypertension and kidney | 1-gen-1984 | Bianchi, G; Ferrari, P; Cusi, D; Guidi, E; Pati, C; Vezzoli, G; Tripodi, G; Niutta, E | |
Genetic impact on renal function decay in radical and partial nephrectomy | 1-gen-2012 | Sciarrone Alibrandi, Mt; Trevisani, F; Delli Carpini, S; Simonini, M; Camerota, T; Merlino, L; Zagato, L; Brioni, E; Bertini, R; Montorsi, Francesco; Rigatti, P; Manunta, Paolo | |
Genetic influence of adducing genes on ischemic strokes. | 1-gen-2013 | Merlino, L; Giacalone, G; Zagato, L; Rainone, F; Sessa, M; Casamassima, N; Simonini, M; Comi, G; Manunta, Paolo | |
Genetic influence on response to serotonergic antidepressants. | 1-gen-2000 | Zanardi, R; Benedetti, F; Serretti, A; Smeraldi, E | |
Genetic Interaction between MTMR2 and FIG4 Phospholipid Phosphatases Involved in Charcot-Marie-Tooth Neuropathies | 1-gen-2011 | Vaccari, I; Dina, G; Tronchere, H; Kaufman, E; Chicanne, G; Cerri, F; Wrabetz, L; Payrastre, B; Quattrini, A; Weisman, Ls; Meisler, Mh; Bolino, A | |
Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration | 1-gen-2009 | Martinelli, P; La Mattina, V; Bernacchia, A; Magnoni, R; Cerri, F; Cox, G; Quattrini, A; Casari, GIORGIO NEVIO; Rugarli, Ei | |
The Genetic Makeup of Myeloproliferative Neoplasms: Role of Germline Variants in Defining Disease Risk, Phenotypic Diversity and Outcome | 1-gen-2021 | Masselli, Elena; Pozzi, Giulia; Carubbi, Cecilia; Vitale, Marco. |
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