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Results:
1-14
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Results: 14
Authors:
Rossi, A
Cerone, R
Biancheri, R
Gatti, R
Schiaffino, MC
Fonda, C
Zammarchi, E
Tortori-Donati, P
Citation: A. Rossi et al., Early-onset combined methylmalonic aciduria and homocystinuria: Neuroradiologic findings, AM J NEUROR, 22(3), 2001, pp. 554-563
Authors:
Biancheri, R
Cerone, R
Schiaffino, MC
Caruso, U
Veneselli, E
Perrone, MV
Rossi, A
Gatti, R
Citation: R. Biancheri et al., Cobalamin (Cbl) C/D deficiency: Clinical, neurophysiological and neuroradiologic findings in 14 cases, NEUROPEDIAT, 32(1), 2001, pp. 14-22
Authors:
Cotellessa, M
Minniti, G
Cerone, R
Prigione, F
Calevo, MG
Lorini, R
Citation: M. Cotellessa et al., Low total plasma homocysteine concentrations in patients with type 1 diabetes, DIABET CARE, 24(5), 2001, pp. 969-970
Authors:
Mudd, SH
Cerone, R
Schiaffino, MC
Fantasia, AR
Minniti, G
Caruso, U
Lorini, R
Watkins, D
Matiaszuk, N
Rosenblatt, DS
Schwahn, B
Rozen, R
LeGros, L
Kotb, M
Capdevila, A
Luka, Z
Finkelstein, JD
Tangerman, A
Stabler, SP
Allen, RH
Wagner, C
Citation: Sh. Mudd et al., Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia, J INH MET D, 24(4), 2001, pp. 448-464
Authors:
Cerone, R
Minniti, G
Piana, A
Armani, U
Lorini, R
Citation: R. Cerone et al., Mild hyperhomocysteinemia: vitamin supplementation or not?, AM J CLIN N, 74(2), 2001, pp. 271-271
Authors:
Minniti, G
Cerone, R
Piana, A
Armani, U
Lorini, R
Citation: G. Minniti et al., Plasma and serum total homocysteine concentrations in paediatric patients,evaluated by high-performance liquid chromatography with fluorescence, CLIN CH L M, 38(7), 2000, pp. 675-676
Authors:
Ruetschi, U
Cerone, R
Perez-Cerda, C
Schiaffino, MC
Standing, S
Ugarte, M
Holme, E
Citation: U. Ruetschi et al., Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type III, HUM GENET, 106(6), 2000, pp. 654-662
Authors:
Cerone, R
Schiaffino, MC
Caruso, U
Gatti, R
Citation: R. Cerone et al., Facial anomalies in combined methylmalonic aciduria and homocystinuria, AM J MED G, 95(1), 2000, pp. 87-87
Authors:
de Sanctis, L
Alliaudi, C
Spada, M
Farrugia, R
Cerone, R
Biasucci, G
Meli, C
Zammarchi, E
Coskun, T
Blau, N
Ponzone, A
Dianzani, I
Citation: L. De Sanctis et al., Genotype-phenotype correlation in dihydropteridine reductase deficiency, J INH MET D, 23(4), 2000, pp. 333-337
Authors:
Cerone, R
Caruso, U
Besley, GTN
Pollitt, RJ
Brown, GK
Hoffmann, GF
Gibson, KM
Citation: R. Cerone et al., The 37th Annual Symposium of the SSIEM - Genova 1999 - Preface, J INH MET D, 23(3), 2000, pp. 195-196
Authors:
Cerone, R
Schiaffino, MC
Di Stefano, S
Veneselli, E
Citation: R. Cerone et al., Phenylketonuria: diet for life or not?, ACT PAEDIAT, 88(6), 1999, pp. 664-666
Authors:
Cerone, R
Schiaffino, MC
Caruso, U
Lupino, S
Gatti, R
Citation: R. Cerone et al., Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolism, J INH MET D, 22(3), 1999, pp. 247-250
Authors:
Minniti, G
Piana, A
Armani, U
Cerone, R
Citation: G. Minniti et al., Determination of plasma and serum homocysteine by high-performance liquid chromatography with fluorescence detection, J CHROMAT A, 828(1-2), 1998, pp. 401-405
Authors:
Balsamo, A
Baserga, M
Burroni, M
Cacciari, E
Cardillo, A
Cassio, A
Cerone, R
Ciatti, R
Cioni, M
Cotugno, G
Forgione, F
Impellizzeri, A
Lelli, A
Lilliu, F
Meli, C
Pagliardini, S
Palillo, L
Parlato, G
Piazzi, S
Pugliese, G
Romano, C
Salardi, S
Torelli, G
Zammarchi, E
Citation: A. Balsamo et al., Screening and diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency, RIV ITAL P, 24(5), 1998, pp. 861-869
Risultati:
1-14
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