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Results:
1-13
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Results: 13
Authors:
Tagliaferro, P
Ramos, AJ
Lopez-Costa, JJ
Lopez, EM
Saavedra, JP
Brusco, A
Citation: P. Tagliaferro et al., Increased nitric oxide synthase activity in a model of serotonin depletion, BRAIN RES B, 54(2), 2001, pp. 199-205
Authors:
Longa, L
Saluto, A
Brusco, A
Polidoro, S
Padovan, S
Allavena, A
Carbonara, C
Grosso, E
Migone, N
Citation: L. Longa et al., TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the gene, HUM GENET, 108(2), 2001, pp. 156-166
Authors:
Mongini, T
Doriguzzi, C
Arduino, C
Brusco, A
Bortolotto, S
Mutani, R
Palmucci, L
Citation: T. Mongini et al., Myopathy in a patient with chromosome 22q11 deletion, NEUROPEDIAT, 32(2), 2001, pp. 107-109
Authors:
DeFranco, S
Bonissoni, S
Cerutti, F
Bona, G
Bottarel, F
Cadario, F
Brusco, A
Loffredo, G
Rabbone, I
Corrias, A
Pignata, C
Ramenghi, U
Dianzani, A
Citation: S. Defranco et al., Defective function of Fas in patients with type 1 diabetes associated withother autoimmune diseases, DIABETES, 50(3), 2001, pp. 483-488
Authors:
Ramenghi, U
Campagnoli, MF
Garelli, E
Carando, A
Brusco, A
Bagnara, GP
Strippoli, P
Izzi, GC
Brandalise, S
Riccardi, R
Dianzani, I
Citation: U. Ramenghi et al., Diamond-Blackfan anemia: Report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population, BL CELL M D, 26(5), 2000, pp. 417-422
Authors:
Rios, H
Lopez-Costa, JJ
Fosser, NS
Brusco, A
Saavedra, JP
Citation: H. Rios et al., Development of nitric oxide neurons in the chick embryo retina, DEV BRAIN R, 120(1), 2000, pp. 17-25
Authors:
Pignata, C
Alessio, M
Ramenghi, U
Bonissoni, S
Difranco, D
Brusco, A
Matrecano, E
Franzese, A
Dianzani, I
Dianzani, U
Citation: C. Pignata et al., Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children, CLIN EXP IM, 121(1), 2000, pp. 53-58
Authors:
Ramos, AJ
Tagliaferro, P
Lopez, EM
Saavedra, JP
Brusco, A
Citation: Aj. Ramos et al., Neuroglial interactions in a model of para-chlorophenylalanine-induced serotonin depletion, BRAIN RES, 883(1), 2000, pp. 1-14
Authors:
Brusco, A
Saviozzi, S
Cinque, F
Bottaro, A
DeMarchi, M
Citation: A. Brusco et al., A recurrent breakpoint in the most common deletion of the Ig heavy chain locus (del A1-GP-G2-G4-E), J IMMUNOL, 163(8), 1999, pp. 4392-4398
Authors:
Arduino, C
Gallo, M
Brusco, A
Garnerone, S
Piana, MR
Di Maggio, S
Promis, GG
Ferrone, M
Angeli, A
Gaia, E
Citation: C. Arduino et al., Polyvariant mutant CFTR genes in patients with chronic pancreatitis, CLIN GENET, 56(5), 1999, pp. 400-404
Authors:
Nardacchione, A
Orsi, L
Brusco, A
Franco, A
Grosso, E
Dragone, E
Mortara, P
Schiffer, D
De Marchi, M
Citation: A. Nardacchione et al., Definition of the smallest pathological CAG expansion in SCA7, CLIN GENET, 56(3), 1999, pp. 232-234
Authors:
Willig, TN
Draptchinskaia, N
Dianzani, I
Ball, S
Niemeyer, C
Ramenghi, U
Orfali, K
Gustavsson, P
Garelli, E
Brusco, A
Tiemann, C
Perignon, JL
Bouchier, C
Cicchiello, L
Dahl, N
Mohandas, N
Tchernia, G
Citation: Tn. Willig et al., Mutations in ribosomal protein S19 gene and Diamond Blackfan anemia: Wide variations in phenotypic expression, BLOOD, 94(12), 1999, pp. 4294-4306
Authors:
Brusco, A
Lopez-Costa, JJ
Tagliaferro, P
Saavedra, JP
Citation: A. Brusco et al., Serotonergic ependymal fibres in rat and monkey: Light and electron microscopic immunocytochemical study, BIOCELL, 22(2), 1998, pp. 115-122
Risultati:
1-13
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