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Internal and Emergency Medicine|September 25, 2010
Porphyrias at a glance: diagnosis and treatmentMaria Domenica Cappellini, Valentina Brancaleoni, Giovanna Graziadei, et al.Annals of Hematology|September 17, 2021
Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 yearsLorena Duca, Isabella Nava, Dario Tavazzi, et al.Blood Cells, Molecules & Diseases|July 4, 2012
Seven novel genetic mutations within the 5'UTR and the housekeeping promoter of HMBS gene responsible for the non-erythroid form of acute intermittent porphyriaValentina Brancaleoni, Francesca Granata, Alessandra Colancecco, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002
Levels of uroporphyrinogen decarboxylase (URO-D) in erythrocytes of Italian porphyria cutanea tarda patientsDario Tavazzi, Franco Martinez di Montemuros, Silvia Fargion, et al.Blood Cells, Molecules & Diseases|July 11, 2006
A large deletion on chromosome 11 in acute intermittent porphyriaElena Di Pierro, Valeria Besana, Valeria Moriondo, et al.American Journal of Nephrology|November 21, 2007
HFE genotype influences erythropoiesis support requirement in hemodialysis patients: a prospective studyLuca Valenti, Giovanni Valenti, Giovanna Como, et al.European Journal of Haematology|November 22, 2008
Cholelithiasis in thalassemia majorRaffaella Origa, Renzo Galanello, Lucia Perseu, et al.Diagnostics (Basel, Switzerland)|August 27, 2021
Laboratory Diagnosis of PorphyriaElena Di Pierro, Michele De Canio, Rosa Mercadante, et al.The Hematology Journal : the Official Journal of the European Haematology Association|December 13, 2003
Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturationClaudio Velati, Eugenia Marlianici, Danila Rigamonti, et al.Pageof 1