Sfoglia per Titolo
L'autore e la danza. La questione della causa in tre dialoghi di Valéry
2012-01-01 Valagussa, Francesco
Autoreactive T cell clones specific for class I and class II HLA antigens isolated from a human chimera
1988-01-01 Roncarolo, MARIA GRAZIA; Yssel, H.; Touraine, J. L.; Betuel, H.; De, Vries; J. E., Spits
Autorità pratica e contenuti impliciti: Freud e Foucault in dialogo con Langton, attraverso Austin
2020-01-01 Ariano, Raffaele
Autoritratto al presente, tra generazioni. Le nuove identità dell’arte italiana
2018-01-01 Pola, Francesca
Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures - A newly recognized epilepsy syndrome with linkage to chromosome 2p11,1-q.12.2
2001-01-01 Guerrini, R; Bonanni, P; Patrignani, A; Brown, P; Parmeggiani, L; Grosse, P; Brovedani, P; Moro, F; Aridon, P; Carrozzo, R; Casari, GIORGIO NEVIO
Autosomal dominant frontal lobe epilepsy
2004-01-01 Combi, R; Dalpra, L; Tenchini, Ml; FERINI STRAMBI, Luigi
Autosomal dominant frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome
1998-01-01 Oldani, A; Zucconi, M; Asselta, R; Modugno, M; Bonati, Mt; Dalpra, L; Malcovati, M; Tenchini, Ml; Smirne, S; FERINI STRAMBI, Luigi
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation
2013-01-01 Galimberti, D; Fenoglio, C; Serpente, M; Villa, C; Bonsi, R; Arighi, A; Fumagalli, Gg; Del Bo, M; Bruni, Ac; Anfossi, M; Clodomiro, A; Cupidi, C; Nacmias, B; Sorbi, S; Piaceri, I; Bagnoli, S; Bessi, V; Marcone, A; Cerami, C; Cappa, Sf; Filippi, M; Agosta, F; Magnani, G; Comi, G; Franceschi, M; Rainero, I; Giordana, Mt; Rubino, E; Ferrero, P; Rogaeva, E; Xi, Z; Confaloni, A; Piscopo, P; Bruno, G; Talarico, G; Cagnin, A; Clerici, F; Dell’Osso, B; Comi, Gp; Altamura, Ac; Mariani, C; Scarpini, E.
Autosomal dominant hereditary spastic paraplegia: report of a large italian family with R581X spastin mutation
2007-01-01 Aridon, P; Ragonese, P; De Fusco, M; Lo Coco, D; Salemi, G; Casari, GIORGIO NEVIO; Savettieri, G.
Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor
2004-01-01 Hu, J; Mora, S; Weber, Giovanna; Zamproni, I; Proverbio, Mc; Spiegel, Am
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome
2006-01-01 Vezzoli, G; Arcidiacono, T; Terranegra, A; Biasion, R; Weber, G; Mora, S; Syren, Ml; Coviello, D; Cusi, D; Bianchi, G; Soldati, L; Paloschi, V; Soldati, L.
Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus
1998-01-01 Scolari, F; Ghiggeri, Gm; Casari, GIORGIO NEVIO; Amoroso, A; Puzzer, D; Caridi, Gl; Valzorio, B; Tardanico, R; Vizzardi, V; Savoldi, S; Viola, Bf; Bossini, N; Prati, E; Gusmano, R; Maiorca, R.
Autosomal dominant migraine with prolonged aura in a family carrying a Notch 3 gene mutation
2000-01-01 Ceroni, M.; Poloni, T. E.; Tognetti, S.; Fabozzi, D.; Uggetti, C.; Frediani, F.; Simonetti, F.; Malaspina, A.; Alimonti, D.; Ferrari, Maurizio; Carrera, P.
Autosomal dominant nocturnal frontal lobe epilepsy: electroclinical picture.
1996-01-01 Oldani, A; Zucconi, M; FERINI STRAMBI, Luigi; Bizzozero, D; 1996 Oct, Smirne S.; 37:964, 7. 6.
Autosomal dominant restless legs syndrome maps on chromosome 14q
2003-01-01 Bonati, Mt; FERINI STRAMBI, Luigi; Aridon, P; Oldani, A; Zucconi, M; Casari, GIORGIO NEVIO
Autosomal dominant tubulointerstitial kidney disease
2019-01-01 Devuyst, O; Olinger, E; Weber, S; Eckardt, Ku; Kmoch, S; Rampoldi, L; Bleyer, Aj
Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature Protein
2019-01-01 Schaeffer, C; Izzi, C; Vettori, A; Pasqualetto, E; Cittaro, D; Lazarevic, D; Caridi, G; Gnutti, B; Mazza, C; Jovine, L; Scolari, F; Rampoldi, L
Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKD
2022-01-01 Econimo, Laura; Schaeffer, Celine; Zeni, Letizia; Cortinovis, Roberta; Alberici, Federico; Rampoldi, Luca; Scolari, Francesco; Izzi, Claudia
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management-A KDIGO consensus report
2015-01-01 Eckardt, Ku; Alper, Sl; Antignac, C; Bleyer, Aj; Chauveau, D; Dahan, K; Deltas, C; Hosking, A; Kmoch, S; Rampoldi, L; Wiesener, M; Wolf, Mt; Devuyst, O
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family
1996-01-01 Quattrone, A; Gambardella, A; Bono, F; Aguglia, U; Bolino, A; Bruni, Ac; Montesi, Mp; Oliveri, Rl; Sabatelli, M; Tamburrini, O; Valentino, P; Vanbroeckhoven, C; Zappia, M
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
L'autore e la danza. La questione della causa in tre dialoghi di Valéry | 1-gen-2012 | Valagussa, Francesco | |
Autoreactive T cell clones specific for class I and class II HLA antigens isolated from a human chimera | 1-gen-1988 | Roncarolo, MARIA GRAZIA; Yssel, H.; Touraine, J. L.; Betuel, H.; De, Vries; J. E., Spits | |
Autorità pratica e contenuti impliciti: Freud e Foucault in dialogo con Langton, attraverso Austin | 1-gen-2020 | Ariano, Raffaele | |
Autoritratto al presente, tra generazioni. Le nuove identità dell’arte italiana | 1-gen-2018 | Pola, Francesca | |
Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures - A newly recognized epilepsy syndrome with linkage to chromosome 2p11,1-q.12.2 | 1-gen-2001 | Guerrini, R; Bonanni, P; Patrignani, A; Brown, P; Parmeggiani, L; Grosse, P; Brovedani, P; Moro, F; Aridon, P; Carrozzo, R; Casari, GIORGIO NEVIO | |
Autosomal dominant frontal lobe epilepsy | 1-gen-2004 | Combi, R; Dalpra, L; Tenchini, Ml; FERINI STRAMBI, Luigi | |
Autosomal dominant frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome | 1-gen-1998 | Oldani, A; Zucconi, M; Asselta, R; Modugno, M; Bonati, Mt; Dalpra, L; Malcovati, M; Tenchini, Ml; Smirne, S; FERINI STRAMBI, Luigi | |
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation | 1-gen-2013 | Galimberti, D; Fenoglio, C; Serpente, M; Villa, C; Bonsi, R; Arighi, A; Fumagalli, Gg; Del Bo, M; Bruni, Ac; Anfossi, M; Clodomiro, A; Cupidi, C; Nacmias, B; Sorbi, S; Piaceri, I; Bagnoli, S; Bessi, V; Marcone, A; Cerami, C; Cappa, Sf; Filippi, M; Agosta, F; Magnani, G; Comi, G; Franceschi, M; Rainero, I; Giordana, Mt; Rubino, E; Ferrero, P; Rogaeva, E; Xi, Z; Confaloni, A; Piscopo, P; Bruno, G; Talarico, G; Cagnin, A; Clerici, F; Dell’Osso, B; Comi, Gp; Altamura, Ac; Mariani, C; Scarpini, E. | |
Autosomal dominant hereditary spastic paraplegia: report of a large italian family with R581X spastin mutation | 1-gen-2007 | Aridon, P; Ragonese, P; De Fusco, M; Lo Coco, D; Salemi, G; Casari, GIORGIO NEVIO; Savettieri, G. | |
Autosomal dominant hypocalcemia in monozygotic twins caused by a de novo germline mutation near the amino-terminus of the human calcium receptor | 1-gen-2004 | Hu, J; Mora, S; Weber, Giovanna; Zamproni, I; Proverbio, Mc; Spiegel, Am | |
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome | 1-gen-2006 | Vezzoli, G; Arcidiacono, T; Terranegra, A; Biasion, R; Weber, G; Mora, S; Syren, Ml; Coviello, D; Cusi, D; Bianchi, G; Soldati, L; Paloschi, V; Soldati, L. | |
Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus | 1-gen-1998 | Scolari, F; Ghiggeri, Gm; Casari, GIORGIO NEVIO; Amoroso, A; Puzzer, D; Caridi, Gl; Valzorio, B; Tardanico, R; Vizzardi, V; Savoldi, S; Viola, Bf; Bossini, N; Prati, E; Gusmano, R; Maiorca, R. | |
Autosomal dominant migraine with prolonged aura in a family carrying a Notch 3 gene mutation | 1-gen-2000 | Ceroni, M.; Poloni, T. E.; Tognetti, S.; Fabozzi, D.; Uggetti, C.; Frediani, F.; Simonetti, F.; Malaspina, A.; Alimonti, D.; Ferrari, Maurizio; Carrera, P. | |
Autosomal dominant nocturnal frontal lobe epilepsy: electroclinical picture. | 1-gen-1996 | Oldani, A; Zucconi, M; FERINI STRAMBI, Luigi; Bizzozero, D; 1996 Oct, Smirne S.; 37:964, 7. 6. | |
Autosomal dominant restless legs syndrome maps on chromosome 14q | 1-gen-2003 | Bonati, Mt; FERINI STRAMBI, Luigi; Aridon, P; Oldani, A; Zucconi, M; Casari, GIORGIO NEVIO | |
Autosomal dominant tubulointerstitial kidney disease | 1-gen-2019 | Devuyst, O; Olinger, E; Weber, S; Eckardt, Ku; Kmoch, S; Rampoldi, L; Bleyer, Aj | |
Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature Protein | 1-gen-2019 | Schaeffer, C; Izzi, C; Vettori, A; Pasqualetto, E; Cittaro, D; Lazarevic, D; Caridi, G; Gnutti, B; Mazza, C; Jovine, L; Scolari, F; Rampoldi, L | |
Autosomal Dominant Tubulointerstitial Kidney Disease: An Emerging Cause of Genetic CKD | 1-gen-2022 | Econimo, Laura; Schaeffer, Celine; Zeni, Letizia; Cortinovis, Roberta; Alberici, Federico; Rampoldi, Luca; Scolari, Francesco; Izzi, Claudia | |
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management-A KDIGO consensus report | 1-gen-2015 | Eckardt, Ku; Alper, Sl; Antignac, C; Bleyer, Aj; Chauveau, D; Dahan, K; Deltas, C; Hosking, A; Kmoch, S; Rampoldi, L; Wiesener, M; Wolf, Mt; Devuyst, O | |
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family | 1-gen-1996 | Quattrone, A; Gambardella, A; Bono, F; Aguglia, U; Bolino, A; Bruni, Ac; Montesi, Mp; Oliveri, Rl; Sabatelli, M; Tamburrini, O; Valentino, P; Vanbroeckhoven, C; Zappia, M |
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