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1. Atypical hemolytic uremic syndrome: Unique clinical presentation linked to rare CFHR5 mutation. Issue 4 (14th September 2021)

2. GENETIC DETERMINANTS OF ACTIVATED FACTOR VII-ANTITHROMBIN COMPLEX (FVIIA-AT) PLASMA LEVELS AND MORTALITY IN PATIENTS WITH ANGIOGRAPHICALLY DEMONSTRATED CORONARY ARTERY DISEASE. (June 2022)

3. Hepcidin and DNA promoter methylation in hepatocellular carcinoma. (28th December 2017)

4. Immunophenotypic Analysis of B Lymphocytes in Patients with Common Variable Immunodeficiency: Identification of CD23 as a Useful Marker in the Definition of the Disease. (4th April 2013)

5. Impaired pro‐resolving mechanisms promote abnormal NETosis, fueling autoimmunity in sickle cell disease. Issue 3 (26th December 2022)

6. Improvement of maternal and fetal outcomes in women with sickle cell disease treated with early prophylactic erythrocytapheresis. Issue 9 (8th July 2018)

7. Metallothioneins Gene Regulation Through Promoter DNA Methylation According to Zn and Cu Trace Elements Status in Human Hepatocellular Carcinoma (P05-002-19). (13th June 2019)