G. Fiorelli

Medicine · Health Sciences

28h-index4.5kcitations155works0.02yr avg
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Research Topics

Iron Metabolism and Disorders(41), Hemoglobinopathies and Related Disorders(39), Liver Disease Diagnosis and Treatment(27), Neonatal Health and Biochemistry(18), Erythrocyte Function and Pathophysiology(15)

Publications155 total

USO DO TACROLIMUS NO TRATAMENTO DAS DOENÇAS ALÉRGICAS GRAVES DA CONJUNTIVA: UMA REVISÃO DE LITERATURA
2024
SERIA O ROCURÔNIO A MELHOR OPÇÃO NA SEQUÊNCIA RÁPIDA DE INTUBAÇÃO? UMA REVISÃO DE LITERATURA
2024
Glucose-6-phosphate dehydrogenase deficiency
The Lancet·2008· 1.5k cited
Coagulation and Splenectomy: An Overview
Annals of the New York Academy of Sciences·2005· 120 cited
Alcohol Dehydrogenase: An Autoantibody Target in Patients with Alcoholic Liver Disease
International Journal of Immunopathology and Pharmacology·2005· 15 citedOpen Access
P117 Preliminary report of a study on the the role of H63D mutation on iron overload in genetic hemochromatosis in Italy
European Journal of Internal Medicine·2003
Clinical and histological evaluation of liver disease in patients with transfusion-dependent beta-thalassemia: A multicenter study
Journal of Hepatology·2003
Increased susceptibility to nonalcoholic fatty liver disease in heterozygotes for the mutation responsible for hereditary hemochromatosis
Digestive and Liver Disease·2003· 97 cited
Iron overload, hfe gene mutations and insulin resistance in non alcoholic fatty liver disease (NAFLD)
Digestive and Liver Disease·2002
65 OP Association between NOD2 mutations and Crohn disease in Italian subjects
Digestive and Liver Disease·2002
Oxidative status and malondialdehyde in β‐thalassaemia patients
European Journal of Clinical Investigation·2002· 136 cited
Red blood cell antioxidant and iron status in alcoholic and nonalcoholic cirrhosis
European Journal of Clinical Investigation·2002· 18 cited
Acute Intermittent Porphyria: Heterogeneity of Mutations in the Hydroxymethylbilane Synthase Gene in Italy
Blood Cells Molecules and Diseases·2001· 17 citedOpen Access
High frequency of the H63D mutation of the hemochromatosis gene (HFE) in malignant gliomas
Neurology·2001· 26 cited
Combination of interferon alpha and ribavirin in chronic hepatitis C non responders to interferon monotherapy: role of genotype and age
Journal of Hepatology·2001· 3 cited
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT)
Human Mutation·2001· 16 cited
TT virus infection in adult beta-thalassemia major patients.
PubMed·2001· 22 cited
A case of pulmonary thromboembolism in thalassemia intermedia: are these patients at risk for thrombotic events?
PubMed·2000· 4 cited
Alcohol-related appearance of Non-Transferrin-Bound Iron (NTBI) in chronic alcohol abusers with cirrhotic and noncirrhotic liver disease
Digestive and Liver Disease·2000
Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia
British Journal of Haematology·2000· 290 cited
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Frequent Co-authors

Maria Domenica Cappellini(22), Maurizio Sampietro(13), Silvia Fargion(12), Alberto Piperno(10), Dario Tavazzi(6), Franco Martinez di Montemuros(5), Anna Ludovica Fracanzani(4), Swee Lay Thein(3), J. S. Wainscoat(3), D. J. Weatherall(3), R. D’Alba(3), Giovanna Graziadei(3), N. Battafarano(2), Lorena Duca(2), Isabella Nava(2), Julie M. Old(2), S. Fargion(2), Luigi F. Bernini(2), N Dioguardi(2), A Agostoni(2)