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Titolo Data di pubblicazione Autore(i) File
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 Polycystic Kidney Disease 1-gen-2010 Ekser, B; Rigotti, Paolo
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
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12-11.2 1-gen-1999 Guerrini, R; Bonanni, P; Nardocci, N; Parmeggiani, L; Piccirilli, M; De Fusco, M; Aridon, P; Ballabio, A; Carrozzo, R; Casari, GIORGIO NEVIO
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