Author/Creator: Fargion, S - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Fargion, S

1. Chronic liver disease in transfusion-dependent thalassaemia: hepatitis B virus marker studies. Issue 10 (October 1980)

Authors:: De Virgiliis, S; Fiorelli, G; Fargion, S; Cornacchia, G; Sanna, G; Cossu, P; Murgia, V; Cao, A
Journal:: Journal of clinical pathology
Issue:: Volume 33:Issue 10(1980)
Page Start:: 949
Record Type:: Journal Article
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2. Early iron overload in beta-thalassaemia major: when to start chelation therapy?. Issue 12 (December 1982)

Authors:: Fargion, S; Taddei, M T; Gabutti, V; Piga, A; Di Palma, A; Capra, L; Fontanelli, G; Avanzini, A
Journal:: Archives of disease in childhood
Issue:: Volume 57:Issue 12(1982)
Page Start:: 929
Record Type:: Journal Article
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3. Evaluation of T and B lymphocytes in liver infiltrates of patients with chronic active hepatitis. Issue 4 (April 1979)

Authors:: Fargion, S; Sangalli, G; Ronchi, G; Fiorelli, G
Journal:: Journal of clinical pathology
Issue:: Volume 32:Issue 4(1979)
Page Start:: 344
Record Type:: Journal Article
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4. Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver disease. (22nd February 2010)

Authors:: Dongiovanni, P; Valenti, L; Rametta, R; Daly, A K; Nobili, V; Mozzi, E; Leathart, J B S; Pietrobattista, A; Burt, A D; Maggioni, M; Fracanzani, A L; Lattuada, E; Zappa, M A; Roviaro, G; Marchesini, G; Day, C P; Fargion, S
Journal:: Gut
Issue:: Volume 59(2010)Supplement 2
Page Start:: 267
Record Type:: Journal Article
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5. Idiopathic haemochromatosis and HLA antigens in Italy: is A3 Bw35 HLA haplotype a marker for idiopathic haemochromatosis gene in north east regions?. Issue 2 (February 1986)

Authors:: Piperno, A; Fargion, S; Panaiotopoulos, N; Del Ninno, E; Taddei, M T; Fiorelli, G
Journal:: Journal of clinical pathology
Issue:: Volume 39:Issue 2(1986)
Page Start:: 125
Record Type:: Journal Article
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6. The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis. Issue 12 (9th December 2004)

Authors:: Valenti, L; Conte, D; Piperno, A; Dongiovanni, P; Fracanzani, A L; Fraquelli, M; Vergani, A; Gianni, C; Carmagnola, L; Fargion, S
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 12(2004)
Page Start:: 946
Record Type:: Journal Article
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