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PreviewIssue DateTitleAuthor(s)AdvisorType
2001Apoptotic Cells In A Peripheral Blood Smear In The Context Of Ebv Infection [2]Pagnano K.B.B.; Vassallo J.; Lorand-Metze I.; Costa F.F.; Saad S.T.O.-Carta
1994Hairy-cell Leukemia And Glucose-6-phosphate Dehydrogenase [1]Arruda V.R.; Saad S.T.O.; Costa F.F.-Carta
2012Hydroxyurea Is Associated With Reductions In Hypercoagulability Markers In Sickle Cell AnemiaColella M.P.; De Paula E.V.; Conran N.; Machado-Neto J.A.; Annicchino-Bizzacchi J.M.; Costa F.F.; Saad S.T.O.; Traina F.-Carta
1993Hepatitis C Antibody (anti-hcv) Prevalence In Brazilian Patients With Sickle Cell Diseases [4]Arruda V.R.; Eid K.A.B.; Zen G.C.; Goncales N.S.; Saad S.T.O.; Costa F.F.-Carta
1990Association Of Pure Red Cell Aplasia And Lepromatous LeprosySaad S.T.O.; Lorand-Metze I.G.H.; Souza C.A.-Carta
1998β-spectrin Promissao: A Translation Initiation Codon Mutation Of The β-spectrin Gene (atg → Gtg) Associated With Hereditary Spherocytosis And Spectrin Deficiency In A Brazilian Family [8]Basseres D.S.; Vicentim D.L.; Costa F.F.; Saad S.T.O.; Hassoun H.-Carta
2003Udp-glucuronosyltransferase 1 Gene Promoter Polymorphism Is Associated With Increased Serum Bilirubin Levels And Cholecystectomy In Patients With Sickle Cell Anemia [1]Fertrin K.Y.; Melo M.B.; Assis A.M.; Saad S.T.O.; Costa F.F.-Carta
2000β 0-thalassemia Resulting From A Novel Mutation: β66/u → Stop Codon [4]Grignoli C.R.E.; Carvalho M.H.; Kimura E.M.; Sonati M.F.; Arruda V.R.; Saad S.T.O.; Costa F.F.-Carta
2000Novel Mutation In The Myoc Gene In Primary Open Angle Glaucoma PatientsVasconcellos J.P.C.; Melo M.B.; Costa V.P.; Tsukumo D.M.L.; Basseres D.S.; Bordin S.; Saad S.T.O.; Costa F.F.-Carta