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Results: 1-13 |
Results: 13
Characterization of the response to myelin basic protein in a non human primate model for multiple sclerosis
Authors: Uccelli, A Giunti, D Mancardi, G Caroli, F Fiorone, M Seri, M Hauser, SL Genain, CP
Citation: A. Uccelli et al., Characterization of the response to myelin basic protein in a non human primate model for multiple sclerosis, EUR J IMMUN, 31(2), 2001, pp. 474-479
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstruction
Authors: De Giorgio, R Seri, M Cogliandro, RF Cusano, R Fava, M Caroli, F Panetta, D Forabosco, P Barbara, G Ravazzolo, R Ceccherini, R Corinaldesi, R Stanghellini, V
Citation: R. De Giorgio et al., Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstruction, CLIN GENET, 59(2), 2001, pp. 131-133
Dynamics of the reactivity to MBP in multiple sclerosis
Authors: Uccelli, A Ristori, G Giunti, D Seri, M Montesperelli, C Caroli, F Solaro, C Murialdo, A Marchese, M Buttinelli, C Mancardi, G Salvetti, M
Citation: A. Uccelli et al., Dynamics of the reactivity to MBP in multiple sclerosis, J NEUROVIRO, 6, 2000, pp. S52-S56
Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome
Authors: Seri, M Melchionda, S Dreyer, S Marini, M Carella, M Cusano, R Piemontese, MR Caroli, F Silengo, M Zelante, L Romeo, G Ravazzolo, R Gasparini, P Lee, B
Citation: M. Seri et al., Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome, INT J MOL M, 4(3), 1999, pp. 285-290
An Asn -> Lys substitution in saposin B involving a conserved amino acidicresidue and leading to the loss of the single N-glycosylation site in a patient with metachromatic leukodystrophy and normal arylsulphatase A activity
Authors: Regis, S Filocamo, M Corsolini, F Caroli, F Keulemans, JLM van Diggelen, OP Gatti, R
Citation: S. Regis et al., An Asn -> Lys substitution in saposin B involving a conserved amino acidicresidue and leading to the loss of the single N-glycosylation site in a patient with metachromatic leukodystrophy and normal arylsulphatase A activity, EUR J HUM G, 7(2), 1999, pp. 125-130
Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME)
Authors: Vitelli, F Piccini, M Caroli, F Franco, B Malandrini, A Pober, B Jonsson, O Sorrentino, V Renieri, A
Citation: F. Vitelli et al., Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME), GENOMICS, 55(3), 1999, pp. 335-340
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndromeand anorectal malformations with sacral hypodevelopment
Authors: Seri, M Martucciello, G Paleari, L Bolino, A Priolo, M Salemi, G Forabosco, P Caroli, F Cusano, R Tocco, T Lerone, M Cama, A Torre, M Guys, JM Romeo, G Jasonni, V
Citation: M. Seri et al., Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndromeand anorectal malformations with sacral hypodevelopment, HUM GENET, 104(1), 1999, pp. 108-110
Pharmacoclinical strategy in neuroleptic resistant schizophrenic patients treated by clozapine: Clinical evolution, concentration of plasma and red blood cell clozapine and desmethylclozapine, whole blood serotonin and tryptophan
Authors: Aymard, N Viala, A Baldacci, C Smagghe, PO Vacheron, MN Caroli, F
Citation: N. Aymard et al., Pharmacoclinical strategy in neuroleptic resistant schizophrenic patients treated by clozapine: Clinical evolution, concentration of plasma and red blood cell clozapine and desmethylclozapine, whole blood serotonin and tryptophan, PROG NEUR-P, 23(1), 1999, pp. 25-41
Congenital hypoplastic anaemia in a patient with a new multiple congenitalanomalies-mental retardation syndrome
Authors: Mori, PG Priolo, M Lerone, M Caroli, F Cusano, R Seri, M Silengo, MC
Citation: Pg. Mori et al., Congenital hypoplastic anaemia in a patient with a new multiple congenitalanomalies-mental retardation syndrome, AM J MED G, 87(1), 1999, pp. 36-39
Mutations in the glucose-6-phosphatase gene of 53 Italian patients with glycogen storage disease type Ia
Authors: Stroppiano, M Regis, S DiRocco, M Caroli, F Gandullia, P Gatti, R
Citation: M. Stroppiano et al., Mutations in the glucose-6-phosphatase gene of 53 Italian patients with glycogen storage disease type Ia, J INH MET D, 22(1), 1999, pp. 43-49
Indications and modalities for electroconvulsive therapy. January 1998
Authors: Darcourt, G Durocher, A Enjalbert, JM Garrabe, J Glikman, J Lienhart, A Paquet, B Pazart, L Auriacombe, M Chevalier, JF Coffinet, P De Carvalho, W Frigard, B Henry, E Lermuzeaux, C Viel, E Allilaire, JF Aulas, JJ Aumond-Veyre, D Bernardet, R Bouvard, M Brudon, F Brun, M Caroli, F Cartier, G Chassagnon, H Chebili, S Colonna, L Gay, MC Gonthier, R Huet, F Koupernik, C Lacore, V Lafont, JP Laurent, V Laxenaire, MC Legrain, S Lepine, JP Loo, H Meignan, ML Michel, F Moritz, P Ourabah, R Pages, M Pages, G Paillere-Martinot, ML Pascal, JC Pedelevental, C Peretti, CS Rousset, H Savet, JF Stael, P Terra, JL Thierry, P Tignol, J Barrier, G Decroix, G Gallois, P Glorion, B Lachaussee, H Laurent, D Sado, P Sargos, P Thouvenin, D
Citation: G. Darcourt et al., Indications and modalities for electroconvulsive therapy. January 1998, SEM HOP PAR, 75(1-2), 1999, pp. 21-26
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy
Authors: Seri, M Cusano, R Forabosco, P Cinti, R Caroli, F Picco, P Bini, R Morra, VB De Michele, G Lerone, M Silengo, M Pela, I Borrone, C Romeo, G Devoto, M
Citation: M. Seri et al., Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy, AM J HU GEN, 64(2), 1999, pp. 586-593
Exclusion of the SCN2B gene as candidate for CMT4B
Authors: Bolino, A Seri, M Caroli, F Eubanks, J Srinivasan, J Mandich, P Schenone, A Quattrone, A Romeo, G Catterall, WA Devoto, M
Citation: A. Bolino et al., Exclusion of the SCN2B gene as candidate for CMT4B, EUR J HUM G, 6(6), 1998, pp. 629-634
Risultati: 1-13 |