ACNP - Italian Periodicals Catalogue

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Results: 1-10 |

Results: 10

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis

Authors: Papanikolaou, G Politou, M Roetto, A Bosio, S Sakelaropoulos, N Camaschella, C Loukopoulos, D

Citation: G. Papanikolaou et al., Linkage to chromosome 1q in Greek families with juvenile hemochromatosis, BL CELL M D, 27(4), 2001, pp. 744-749

A new mutation trans to 1278T cystathionine beta-synthase associated with Factor V Leiden causes mild homocystinuria but severe vascular disease

Authors: Bosio, S Cavallero, G Brusa, E Alberti, F Camaschella, C

Citation: S. Bosio et al., A new mutation trans to 1278T cystathionine beta-synthase associated with Factor V Leiden causes mild homocystinuria but severe vascular disease, THROMB HAEM, 86(2), 2001, pp. 716-717

Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome

Authors: Girelli, D Bozzini, C Zecchina, G Tinazzi, E Bosio, S Piperno, A Ramenghi, U Peters, J Levi, S Camaschella, C Corrocher, R

Citation: D. Girelli et al., Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome, BR J HAEM, 115(2), 2001, pp. 334-340

G20210A homozygosity in antiphospholipid syndrome secondary to systemic lupus erythematosus

Authors: Sivera, P Bosio, S Bertero, MT Demaestri, M Mazza, U Camaschella, C

Citation: P. Sivera et al., G20210A homozygosity in antiphospholipid syndrome secondary to systemic lupus erythematosus, HAEMATOLOG, 85(1), 2000, pp. 109-110

Haemochromatosis in patients with beta-thalassaemia trait

Authors: Piperno, A Mariani, R Arosio, C Vergani, A Bosio, S Fargion, S Sampietro, M Girelli, D Fraquelli, M Conte, D Fiorelli, G Camaschella, C

Citation: A. Piperno et al., Haemochromatosis in patients with beta-thalassaemia trait, BR J HAEM, 111(3), 2000, pp. 908-914

Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome

Authors: Cicilano, M Zecchina, G Roetto, A Bosio, S Infelise, V Stefani, S Mazza, U Camaschella, C

Citation: M. Cicilano et al., Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome, HAEMATOLOG, 84(6), 1999, pp. 489-492

Variation in the phenotypic expression of C282Y hemochromatosis in an Italian family

Authors: Bosio, S Zecchina, G Cicilano, M Roetto, A Saito, AM Camaschella, C

Citation: S. Bosio et al., Variation in the phenotypic expression of C282Y hemochromatosis in an Italian family, HAEMATOLOG, 84(2), 1999, pp. 184-185

Inherited HFE-unrelated hemochromatosis in Italian families

Authors: Camaschella, C Fargion, S Sampietro, M Roetto, A Bosio, S Garozzo, G Arosio, C Piperno, A

Citation: C. Camaschella et al., Inherited HFE-unrelated hemochromatosis in Italian families, HEPATOLOGY, 29(5), 1999, pp. 1563-1564

Pain and affective disorders in 183 aged geriatric inpatients

Authors: Radat, F Servant-Marcucci, S Bosio, S Alla, P

Citation: F. Radat et al., Pain and affective disorders in 183 aged geriatric inpatients, ANN MED PSY, 157(10), 1999, pp. 736-739

Juvenile hemochromatosis locus maps to chromosome 1q

Authors: Roetto, A Totaro, A Cazzola, M Cicilano, M Bosio, S D'Ascola, G Carella, M Zelante, L Kelly, AL Cox, TM Gasparini, P Camaschella, C

Citation: A. Roetto et al., Juvenile hemochromatosis locus maps to chromosome 1q, AM J HU GEN, 64(5), 1999, pp. 1388-1393

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