Browsing by Author Costa F.F.

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

or enter first few letters:  
Showing results 1 to 20 of 137  next >
PreviewIssue DateTitleAuthor(s)AdvisorType
2014Guidelines On The Treatment Of Anemia Of Chronic Renal Failure Using Recombinant Human Erythropoietin: Associação Brasileira De Hematologia, Hemoterapia E Terapia Celular Guidelines Project: Associação Médica Brasileira - 2014da Silva Araujo A.; de Castro Lobo C.L.; Covas D.T.; Costa F.F.; Medeiros L.; Cancado R.D.; Gualandro S.F.M.; Saad S.T.O.-Artigo de periódico
2015Investigating Alpha-globin Structural Variants: A Retrospective Review Of 135,000 Brazilian IndividualsKimura E.M.; Oliveira D.M.; Jorge S.E.; Ribeiro D.M.; Zaccariotto T.R.; Santos M.N.N.; Almeida V.; Albuquerque D.M.; Costa F.F.; Sonati M.D.F.-Artigo de periódico
2008Identification Of Characterization Of Novel And Rare Variants Of Human Hemoglobin [identificação E Caracterização De Variantes Novas E Raras Da Hemoglobina Humana]Kimura E.M.; Oliveira D.M.; Jorge S.E.D.C.; Abreu C.F.; Albuquerque D.M.; Costa F.F.; De Sonati M.F.-Artigo de periódico
2008Arhgap21 Associates With Fak And Pkcζ And Is Redistributed After Cardiac Pressure OverloadBorges L.; Bigarella C.L.; Baratti M.O.; Crosara-Alberto D.P.; Joazeiro P.P.; Franchini K.G.; Costa F.F.; Saad S.T.O.-Artigo de periódico
2014Hydroxycarbamide Reduces Eosinophil Adhesion And Degranulation In Sickle Cell Anaemia PatientsPallis F.R.; Conran N.; Fertrin K.Y.; Olalla Saad S.T.; Costa F.F.; Franco-Penteado C.F.-Artigo de periódico
2009Hemoglobin Disorders And Endothelial Cell InteractionsConran N.; Costa F.F.-Artigo de periódico
2009High Levels Of Human γ-globin Are Expressed In Adult Mice Carrying A Transgene Of The Brazilian Type Of Hereditary Persistence Of Fetal Hemoglobin (aγ -195)Da Cunha A.F.; Brugnerotto A.F.; Finzi Corat M.A.; Devlin E.E.; Gimenes A.P.; Barbosa De Melo M.; Corra Passos L.A.; Bodine D.; Saad S.T.O.; Costa F.F.-Artigo de periódico
2009Two New Unstable Haemoglobins Leading To Chronic Haemolytic Anaemia: Hb Caruaru [β122 (gh5) Phe→ser], A Probable Case Of Germ Line Mutation, And Hb Olinda [β22 (b4) - 25 (b7)], A Deletion Of A 12 Base-pair SequenceBezerra M.A.C.; Albuquerque D.M.; Santos M.N.N.; Kimura E.M.; Jorge S.E.D.C.; Oliveira D.M.; Domingues B.L.T.B.; Peres J.C.; Araujo A.S.; Costa F.F.; Sonati M.F.-Artigo de periódico
2009Pip4kiia And β-globin: Transcripts Differentially Expressed In Reticulocytes And Associated With High Levels Of Hb H In Two Siblings With Hb H DiseaseWenning M.R.S.C.; Mello M.P.; Andrade T.G.; Lanaro C.; Albuquerque D.M.; Saad S.T.O.; Costa F.F.; Sonati M.F.-Artigo de periódico
1996Expression Of Spectrin α(i/65) Hereditary Elliptocytosis In Patients From BrazilPranke P.H.L.; Basseres D.S.; Costa F.F.; Saad S.T.O.-Artigo de periódico
1996Rapid Detection Of Factor V Leiden (fvq506) By Non-radioactive Single Strand Conformation Polymorphism (sscp)Arruda V.R.; Von Zuben P.M.; Annichino-Bizzachi J.M.; Costa F.F.-Artigo de periódico
1995Factor V Leiden (fvq 506) Is Common In A Brazilian PopulationArruda V.R.; Annichino-Bizzacchi M.; Costa F.F.; Reitsma P.H.-Artigo de periódico
1995Molecular Identification Of Hereditary Persistence Of Fetal Hemoglobin Type 2 (hpfh Type 2) In Patients From BrazilGoncalves M.S.; Fahel S.; Figueiredo M.S.; Kimura E.J.; Nechtman F.; Stoming T.A.; Arruda V.R.; Saad S.T.O.; Costa F.F.-Artigo de periódico
2009Newer Aspects Of The Pathophysiology Of Sickle Cell Disease Vaso-occlusionConran N.; Franco-Penteado C.F.; Costa F.F.-Artigo de periódico
2001Hydroxyurea Promotes The Reduction Of Spontaneous Bfu-e To Normal Levels In Ss And S/β Thalassemic PatientsBincoletto C.; Perlingeiro R.C.R.; Saad S.T.O.; Costa F.F.; Queiroz M.L.S.-Artigo de periódico
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
2001High Prevalence Of α-thalassemia Among Individuals With Microcytosis And Hypochromia Without AnemiaBorges E.; Wenning M.R.S.C.; Kimura E.M.; Gervasio S.A.; Costa F.F.; Sonati M.F.-Artigo de periódico
2001The Aγ-195 (c→g) Mutation In Hereditary Persistence Of Fetal Hemoglobin Is Not Associated With Activation Of A Reporter Gene In VitroSchreiber R.; Goncalves M.S.; Junqueira M.L.; Saad S.T.O.; Krieger J.E.; Costa F.F.-Artigo de periódico
1996Effect Of α-thalassemia And β-globin Gene Cluster Haplotypes On The Hematological And Clinical Features Of Sickle-cell Anemia In BrazilFigueiredo M.S.; Kerbauy J.; Goncalves M.S.; Arruda V.R.; Saad S.T.O.; Sonati M.F.; Stoming T.; Costa F.F.-Artigo de periódico
1996Hb Camperdown [α2β2104(g6)arg→ser] Identified By Dna Analysis In A Brazilian FamilyMiranda S.R.P.; Kimura E.M.; Teixeira R.C.; Bertuzzo C.S.; Ramalho A.S.; Saad S.T.O.; Costa F.F.-Artigo de periódico