Corrocher, Roberto
University of Verona
8 papers on CoChat
Most cited papers
- Verified
Prevalence of Body Iron Excess in the Metabolic Syndrome
Bozzini, C., Girelli, D., Olivieri, O., Martinelli, N., Bassi, A., De Matteis, G., Tenuti, I., Lotto, V., Friso, S., Pizzolo, F., et al. (2005) · Diabetes Care
Iron Metabolism and DisordersDiabetes, Cardiovascular Risks, and Lipoproteins
Cited by 224
- Verified
Molecular basis for the recently described hereditary hyperferritinemia- cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation") [see comments]
Girelli, D., Corrocher, R., Bisceglia, L., Olivieri, O., De Franceschi, L., Zelante, L., & Gasparini, P. (1995) · Blood
Iron Metabolism and DisordersNeurological diseases and metabolism
Cited by 196
- Verified
Reduced serum hepcidin levels in patients with chronic hepatitis C
Girelli, D., Pasino, M., Goodnough, J. B., Nemeth, E., Guido, M., Castagna, A., Busti, F., Campostrini, N., Martinelli, N., Vantini, I., et al. (2009) · Journal of Hepatology
Iron Metabolism and DisordersHepatitis C virus research
Cited by 169
- Verified
Apolipoprotein C-III, metabolic syndrome, and risk of coronary artery disease
Olivieri, O., Bassi, A., Stranieri, C., Trabetti, E., Martinelli, N., Pizzolo, F., Girelli, D., Friso, S., Pignatti, P. F., & Corrocher, R. (2003) · Journal of Lipid Research
Lipid metabolism and disordersDiabetes, Cardiovascular Risks, and Lipoproteins
Cited by 139
- Verified
Analysis of Ferritins in Lymphoblastoid Cell Lines and in the Lens of Subjects With Hereditary Hyperferritinemia-Cataract Syndrome
Levi, S., Girelli, D., Perrone, F., Pasti, M., Beaumont, C., Corrocher, R., Albertini, A., & Arosio, P. (1998) · Blood
Iron Metabolism and DisordersNeurological diseases and metabolism
Cited by 96
- Verified
Low selenium status in the elderly influences thyroid hormones
Olivieri, O., Girelli, D., Azzini, M., Stanzial, A. M., Russo, C., Ferroni, M., & Corrocher, R. (1995) · Clinical Science
Selenium in Biological SystemsThyroid Disorders and Treatments
Cited by 95
- Verified
ApoC-III gene polymorphisms and risk of coronary artery disease
Olivieri, O., Stranieri, C., Bassi, A., Zaia, B., Girelli, D., Pizzolo, F., Trabetti, E., Cheng, S., Grow, M. A., Pignatti, P. F., et al. (2002) · Journal of Lipid Research
Lipid metabolism and disordersLipoproteins and Cardiovascular Health
Cited by 70
- Verified
Apolipoprotein C-III, n-3 polyunsaturated fatty acids, and “insulin-resistant” T-455C APOC3 gene polymorphism in heart disease patients: example of gene-diet interaction
Olivieri, O., Martinelli, N., Sandri, M., Bassi, A., Guarini, P., Trabetti, E., Pizzolo, F., Girelli, D., Friso, S., Pignatti, P. F., et al. (2005) · Clinical Chemistry
Fatty Acid Research and HealthLipid metabolism and disorders
Cited by 50
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