Cristina Vercellati
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
49 papers found
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Cerebellar atrophy in a child with hereditary methemoglobinemia type II
Download from www.researchgate.netHereditary red cell membrane defects: diagnostic and clinical aspects
Download from doi.orgCongenital dyserythropoietic anemia type II (CDAII) is caused by mutations in theSEC23Bgene
Download from www.researchgate.netBlood p50 evaluation enhances diagnostic definition of isolated erythrocytosis
Download from www.researchgate.netRed cell pyruvate kinase deficiency: 17 new mutations of the PK-LR gene
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