Sfoglia per Autore  

Opzioni
Mostrati risultati da 21 a 34 di 34
Titolo Data di pubblicazione Autore(i) File
The natural history of Aicardi-Goutières syndrome: follow-up of 11 Italian patients 1-gen-2005 Lanzi, Giovanni; Fazzi, ELISA MARIA; D'Arrigo, S; Orcesi, S; Maraucci, I; Uggetti, C; Bertini, E; Lebon, P.
Towards improved clinical charaterization of Leber congenital amaurosis. Neurological and systemic findings 1-gen-2005 Fazzi, ELISA MARIA; Signorini, Sg; Uggetti, C; Bianchi, Pe; Lanners, J; Lanzi, Giovanni
Towards improved clinical characterization of Leber congenital amaurosis: neurological and systemic findings. 1-gen-2005 Fazzi, ELISA MARIA; Signorini, SABRINA GIOVANNA; Uggetti, C.; Bianchi, PAOLO EMILIO; Lanners, J.; Lanzi, Giovanni
The ketogenic diet: from molecular mechanisms to clinical effects 1-gen-2006 Freeman, J; Veggiotti, Pierangelo; Lanzi, Giovanni; Tagliabue, Anna; Perucca, Emilio
A pilot study of a ketogenic diet in patients with Lafora body disease 1-gen-2006 Cardinali, S.; Canafoglia, L.; Bertoli, S.; Franceschetti, S.; Lanzi, Giovanni; Tagliabue, Anna; Veggiotti, Pierangelo
Clinical and molecular phenotype of aicardi-goutieres syndrome. 1-gen-2007 Rice, G; Patrick, T; Parmar, R; Taylor, Cf; Aeby, A; Aicardi, J; Artuch, R; Montalto, Sa; Bacino, Ca; Barroso, B; Baxter, P; Benko, Ws; Bergmann, C; Bertini, E; Biancheri, R; Blair, Em; Blau, N; Bonthron, Dt; Briggs, T; Brueton, La; Brunner, Hg; Burke, Cj; Carr, Im; Carvalho, Dr; Chandler, Ke; Christen, Hj; Corry, Pc; Cowan, Fm; Cox, H; D'Arrigo, S; Dean, J; De Laet, C; De Praeter, C; Dery, C; Ferrie, Cd; Flintoff, K; Frints, Sg; Garcia Cazorla, A; Gener, B; Goizet, C; Goutieres, F; Green, Aj; Guet, A; Hamel, Bc; Hayward, Be; Heiberg, A; Hennekam, Rc; Husson, M; Jackson, Ap; Jayatunga, R; Jiang, Yh; Kant, Sg; Kao, A; King, Md; Kingston, Hm; Klepper, J; van der Knaap, Ms; Kornberg, Aj; Kotzot, D; Kratzer, W; Lacombe, D; Lagae, L; Landrieu, Pg; Lanzi, Giovanni; Leitch, A; Lim, Mj; Livingston, Jh; Lourenco, Cm; Lyall, Eg; Lynch, Sa; Lyons, Mj; Marom, D; Mcclure, Jp; Mcwilliam, R; Melancon, Sb; Mewasingh, Ld; Moutard, Ml; Nischal, Kk; Ostergaard, Jr; Prendiville, J; Rasmussen, M; Rogers, Rc; Roland, D; Rosser, Em; Rostasy, K; Roubertie, A; Sanchis, A; Schiffmann, R; Scholl Burgi, S; Seal, S; Shalev, Sa; Corcoles, Cs; Sinha, Gp; Soler, D; Spiegel, R; Stephenson, Jb; Tacke, U; Tan, Ty; Till, M; Tolmie, Jl; Tomlin, P; Vagnarelli, F; Valente, ENZA MARIA; Van Coster, Rn; Van der Aa, N; Vanderver, A; Vles, Js; Voit, T; Wassmer, E; Weschke, B; Whiteford, Ml; Willemsen, Ma; Zankl, A; Zuberi, Sm; Orcesi, S; Fazzi, ELISA MARIA; Lebon, P; Crow, Y. J.
Leber's congenital amaurosis: is there an autistic component? 1-gen-2007 Fazzi, ELISA MARIA; Rossi, M.; Signorini, SABRINA GIOVANNA; Rossi, Giorgio; Bianchi, PAOLO EMILIO; Lanzi, Giovanni
Pharmacological Treatment of Anorexia Nervosa: A retrospective Study in Preadolescents and Adolescents. 1-gen-2007 Rossi, Giorgio; Balottin, Umberto; Rossi, M; Chiappedi, M; Fazzi, E; Lanzi, Giovanni
Dopaminergic receptor D5 mRNA expression is increased in circulating lymphocytes of Tourette syndrome patients 1-gen-2008 Ferrari, M; Termine, Cristiano; Franciotta, Diego; Castiglioni, E; Pagani, A; Lanzi, Giovanni; Marino, F; Lecchini, S; Cosentino, M; Balottin, Umberto
Migraine with aura with onset in childhood and adolescence: long-term natural history and prognostic factors 1-gen-2010 Termine, Cristiano; M., Ferri; G., Livetti; E., Beghi; S., Salini; A., Mongelli; R., Blangiardo; Lanzi, Giovanni; Balottin, Umberto
Generation of three isogenic induced Pluripotent Stem Cell lines (iPSCs) from fibroblasts of a patient with Aicardi Goutières Syndrome carrying a c.2471G>A dominant mutation in IFIH1 gene 1-gen-2019 Masneri, S.; Lanzi, G.; Ferraro, R. M.; Barisani, C.; Piovani, G.; Savio, G.; Cattalini, M.; Galli, J.; Cereda, C.; Muzi-Falconi, M.; Orcesi, S.; Fazzi, E.; Giliani, S.
Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1 1-gen-2019 Ferraro, R. M.; Lanzi, G.; Masneri, S.; Barisani, C.; Piovani, G.; Savio, G.; Cattalini, M.; Galli, J.; Cereda, C.; Muzi-Falconi, M.; Orcesi, S.; Fazzi, E.; Giliani, S.
Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B 1-gen-2019 Ferraro, R. M.; Masneri, S.; Lanzi, G.; Barisani, C.; Piovani, G.; Savio, G.; Cattalini, M.; Galli, J.; Cereda, C.; Muzi-Falconi, M.; Orcesi, S.; Fazzi, E.; Giliani, S.
Biomarkers and Precision Therapy for Primary Immunodeficiencies: An In Vitro Study Based on Induced Pluripotent Stem Cells From Patients 1-gen-2020 Genova, E.; Cavion, F.; Lucafo, M.; Pelin, M.; Lanzi, G.; Masneri, S.; Ferraro, R. M.; Fazzi, E. M.; Orcesi, S.; Decorti, G.; Tommasini, A.; Giliani, S.; Stocco, G.
Mostrati risultati da 21 a 34 di 34
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