Dario Tavazzi

University of Milan — Italy

Medicine · Health Sciences

17h-index965citations57works0.02yr avg
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Research Topics

Neonatal Health and Biochemistry(22), Porphyrin Metabolism and Disorders(22), Hemoglobinopathies and Related Disorders(17), Iron Metabolism and Disorders(12), Metabolism and Genetic Disorders(11)

Publications57 total

04131 Increased pancreatic enzymes in a patient with acute intermittent porphyria
2024Open Access
Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 years
Annals of Hematology·2021· 3 cited
Laboratory Diagnosis of Porphyria
Diagnostics·2021· 52 citedOpen Access
Microcytosis in Erythropoietic Protoporphyria
Blood·2020· 1 cited
UGT1A1 genotype does not affect tyrosine kinase inhibitors efficacy and safety in chronic myeloid leukemia
American Journal of Hematology·2019· 5 citedOpen Access
PF432 EPIDEMIOLOGICAL SHIFT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) MUTATIONS IN NORTHERN ITALY DURING THE LAST 15 YEARS
HemaSphere·2019Open Access
Circulating cell‐free DNA and ineffective erythropoiesis in nontransfusion‐dependent β‐thalassemia
American Journal of Hematology·2018· 3 citedOpen Access
Corrigendum to “Seven novel genetic mutations within the 5′ UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria” [Blood Cells Mol. Dis. 49 (2012) 147–151]
Blood Cells Molecules and Diseases·2016· 4 cited
Seven novel genetic mutations within the 5′UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyria
Blood Cells Molecules and Diseases·2012· 14 cited
260 ABERRANT METHYLATION OF ONCOSUPPRESSOR GENES DETECTED IN THE PERIPHERAL BLOOD OF PATIENTS WITH CHRONIC HEPATITIS C AND HEPATOCELLULAR CARCINOMA
Journal of Hepatology·2011· 1 citedOpen Access
Hypermethylation of oncosuppressor genes in hereditary hemochromatosis
2010
Porphyrias at a glance: diagnosis and treatment
Internal and Emergency Medicine·2010· 23 cited
Clinical, biochemical and genetic characteristics of Variegate Porphyria in Italy.
PubMed·2009· 19 cited
C-terminal deletion in the ALAS2 gene and X-linked dominant protoporphyria
2009· 3 cited
Identification of Three Novel Substitutions in the Erythroid Promoter of the HMBS Gene: A New Erythroid Variant of Human Acute Intermittent Porphyria?
Blood·2008
A novel mutation in the first italian patient of hereditary coproporphyria
2008
Molecular heterogeneity of variegate porphyria in Italy
2008
Cholelithiasis in thalassemia major
European Journal Of Haematology·2008· 36 citedOpen Access
Beta-thalassemia Intermedia: An Overview
Pediatric Annals·2008· 12 cited
Red blood cell enzyme disorders: An overview
Scopus·2008Open Access
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Frequent Co-authors

Maria Domenica Cappellini(32), Elena Di Pierro(15), Franco Martinez di Montemuros(15), Gemino Fiorelli(14), Maurizio Sampietro(12), Silvia Fargion(11), G. Fiorelli(10), Lorena Duca(9), Valentina Brancaleoni(9), Giovanna Graziadei(8), Francesca Granata(5), Cappellini(5), Emilio Rocchi(5), Anna Ludovica Fracanzani(4), Luca Valenti(4), A. Comino(4), Valeria Besana(4), Chiara Dotti(3), C. Bertelli(3), Valeria Moriondo(3)