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2. Clinical and genetic characteristics of late-onset Huntington's disease. (April 2019)

4. HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype‐phenotype correlation. (12th December 2019)

5. Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes. Issue 6 (28th August 2019)

6. VKORC1 and CYP2C9 polymorphisms related to adverse events in case-control cohort of anticoagulated patients. Issue 52 (December 2016)

7. VKORC1 and CYP2C9 polymorphisms related to adverse events in case-control cohort of anticoagulated patients. Issue 52 (December 2016)

8. Y-chromosome haplogroups and susceptibility to azoospermia factor c microdeletion in an Italian population. Issue 3 (8th December 2006)