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Sara Teresinha Olalla Saad
Sara Teresinha Olalla Saad
Professora Titular da Disciplina de Hematologia e Hemoterapia, Universidade Estadual de Campinas
E-mail confirmado em unicamp.br
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Citado por
Citado por
Ano
ANEMIAS POR DEFEITOS DE MEMBRANA ERITROCITÁRIA IN Hematologia: Fundamentos e Prática
STOSEDMA Zago, RP Falcão, R Pasquim
Atheneu, 2001
427*2001
Impact of molecular mutations on treatment response to DNMT inhibitors in myelodysplasia and related neoplasms
F Traina, V Visconte, P Elson, A Tabarroki, AM Jankowska, E Hasrouni, ...
Leukemia 28 (1), 78-87, 2014
3652014
Optical tweezers for measuring red blood cell elasticity: application to the study of drug response in sickle cell disease
MM Brandao, A Fontes, ML Barjas‐Castro, LC Barbosa, FF Costa, ...
European journal of haematology 70 (4), 207-211, 2003
3012003
Probiotics modulate gut microbiota and improve insulin sensitivity in DIO mice
RA Bagarolli, N Tobar, AG Oliveira, TG Araújo, BM Carvalho, GZ Rocha, ...
The Journal of nutritional biochemistry 50, 16-25, 2017
2612017
Altered levels of cytokines and inflammatory mediators in plasma and leukocytes of sickle cell anemia patients and effects of hydroxyurea therapy
C Lanaro, CF Franco-Penteado, DM Albuqueque, STO Saad, N Conran, ...
Journal of Leucocyte Biology 85 (2), 235-242, 2009
2392009
An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis
LM Hollanda, CSP Lima, AF Cunha, DM Albuquerque, J Vassallo, ...
Nature genetics 38 (7), 807-812, 2006
2152006
Defeitos Hereditários da Membrana In: Tratado de Clínica Médica
STOSEDAC Lopes
Roca, 2006
205*2006
Single Nucleotide Polymorphism Array Lesions, TET2, DNMT3A, ASXL1 and CBL Mutations Are Present in Systemic Mastocytosis
F Traina, V Visconte, AM Jankowska, H Makishima, CL O’Keefe, P Elson, ...
Public Library of Science 7 (8), e43090, 2012
1232012
Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: Relevance to …
VR Arruda, CE Grignolli, MS Gonçalves, MC Soares, R Menezes, ...
Clinical genetics 54 (3), 210, 1998
1221998
Prevalence of the homozygous for the deleted alleles of glutathione S transferase Um (GSTM1) and Theta (GSTT1) among distinct ethnic grups from Brazil: relevance to …
VR Arruda, F Andrade, JM Annichino-Bizzacchi, STO Saad, FF Costa
Clinical Genetics 54, 210-214, 1998
122*1998
Effect of alpha thalassemia and beta globin gene cluster haplotyes on the Hematological and Clinical features of sickle cell anemia
MS Figueiredo, J Kerbauy, MS Gonçalves, VR Arruda, STO Saad, ...
American Journal of Hematology 53, 72-76, 1996
1191996
DNA‐based typing of blood groups for the management of multiply‐transfused sickle cell disease patients
L Castilho, M Rios, C Bianco, J Pellegrino Jr, FL Alberto, STO Saad, ...
Transfusion 42 (2), 232-238, 2002
1172002
Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).
P Jarolim, HL Rubin, SC Liu, MR Cho, V Brabec, LH Derick, SJ Yi, ...
The Journal of clinical investigation 93 (1), 121-130, 1994
1171994
Increased risk for acute myeloid leukaemia
in individuals with glutathione S‐transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects
VR Arruda, CSP Lima, CRE Grignoli, MB De Melo, I Lorand‐Metze, ...
European journal of haematology 66 (6), 383-388, 2001
1002001
Pancytopenia in untreated patients with Graves' disease
CSP Lima, DEZ Wittmann, V Castro, MA Tambascia, I Lorand-Metze, ...
Thyroid 16 (4), 403-409, 2006
962006
Increased adhesive properties of neutrophils in sickle cell disease may be reversed by pharmacological nitric oxide donation
AA Canalli, CF Franco-Penteado, STO Saad, N Conran, FF Costa
haematologica 93 (4), 605-609, 2008
922008
Differentiation of C2C12 myoblasts is critically regulated by FAK signaling
CFMZ Clemente, MAF Corat, STO Saad, KG Franchini
American Journal of Physiology-Regulatory, Integrative and Comparative …, 2005
912005
A novel mutation in the anion exchanger 1 gene is associated with familial distal renal tubular acidosis and nephrocalcinosis
L Cheidde, TC Vieira, PRM Lima, STO Saad, IP Heilberg
Pediatrics 112 (6), 1361-1367, 2003
912003
Follow‐up of sickle cell disease patients with priapism treated by hydroxyurea
STO Saad, C Lajolo, S Gilli, JFC Marques Jr, CS Lima, FF Costa, ...
American journal of hematology 77 (1), 45-49, 2004
862004
Mechanical properties of stored red blood cells using optical tweezers
RR Huruta, ML Barjas-Castro, STO Saad, FF Costa, A Fontes, ...
Blood, The Journal of the American Society of Hematology 92 (8), 2975-2977, 1998
861998
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