Helena Grotto - Academia.edu (original) (raw)
Papers by Helena Grotto
Revista Brasileira De Hematologia E Hemoterapia, 2009
Revista Brasileira De Hematologia E Hemoterapia, Jun 1, 2010
Revista Brasileira De Hematologia E Hemoterapia, Jan 6, 2010
American Journal of Hematology, 2005
Although it is almost certain that α+‐thalassemia protects against malaria, the mechanisms for th... more Although it is almost certain that α+‐thalassemia protects against malaria, the mechanisms for that are still unknown. It has been suggested that an increased number of young circulating red blood cells in α+‐thalassemic children, as a result of some degree of ineffective erythropoiesis, could be related to the high frequencies of the α+‐thalassemic allele in malaria endemic areas. Reticulocyte evaluation in this condition, however, has been poorly performed so far. Our objective was to determine the reticulocyte number and maturation degree, in addition to the soluble transferrin receptor and serum erythropoietin levels, in α+‐thalassemia heterozygotes, comparing them with normal α‐genotype controls. One hundred twenty‐one α+‐thalassemia carriers (−α3.7/αα) and 249 controls (αα/αα), all of them with normal serum ferritin levels, were subclassified according to age (1–5, 6–10, 11–15, 16–20, and over 20 years old). Reticulocyte analyzes were carried out by flow cytometry and sTfR and s‐Epo levels determined by immunonephelometry and chemiluminescence, respectively. The comparisons did not show any significant difference between thalassemics and controls regarding the reticulocyte parameters [percentages and absolute values, P = 0.2643 and 0.5421; high, medium, and low maturation degree, P = 0.2579, 0.2196, and 0.4192; RET maturity index (RMI), P = 0.2471, respectively], as well as the s‐Epo levels (P = 0.5711). The sTfR concentrations were higher in the thalassemic group (P = 0.0001), but statistical significance was due only to the 1–5 and over 20 subgroups (P = 0.0082 and 0.0436, respectively). The results found here are compatible with a compensated erythropoiesis and do not confirm the hypothesis mentioned above. Am. J. Hematol. 81:68–70, 2006. © 2005 Wiley‐Liss, Inc.
Revista Brasileira De Hematologia E Hemoterapia, Oct 1, 2008
Revista Brasileira De Hematologia E Hemoterapia, Oct 1, 2008
Revista Brasileira De Hematologia E Hemoterapia, 2009
Acta Haematologica, 1992
Clinical, laboratory features and restriction enzyme DNA analysis are reported for a black Brazil... more Clinical, laboratory features and restriction enzyme DNA analysis are reported for a black Brazilian woman with HbH disease. The patient presented a thalassemic blood picture with HbH and Hb Bart’s. Gene mapping demonstrated the compound heterozygous state for the --MED and -α3.7 deletions.Copyright © 1992 S. Karger AG, Basel
Journal of Clinical Laboratory Analysis, 2006
Revista Brasileira de Hematologia e Hemoterapia, 2016
Revista Brasileira de Hematologia e Hemoterapia, 2009
Revista Brasileira de Hematologia e Hemoterapia, 2008
Jornal Brasileiro de Patologia e Medicina Laboratorial, 2002
BioMed Research International, 2014
The aim of this study was to establish reference intervals (RIs) for the hemogram and iron status... more The aim of this study was to establish reference intervals (RIs) for the hemogram and iron status biomarkers in a physically active population. The study population included male volunteers (n=150) with an average age of 19 ± 1 years who had participated in a regular and controlled exercise program for four months. Blood samples were collected to determine hematological parameters using a Sysmex XE-5000 analyzer (Sysmex, Kobe, Japan). Iron, total iron-binding capacity (TIBC), transferrin saturation and ferritin, and high-sensitivity C-reactive protein (CRP) concentrations in serum samples were measured using commercial kits (Roche Diagnostics, GmbH, Mannheim, Germany) and a Roche/Hitachi 902 analyzer. The RIs were established using the RefVal program 4.1b. The leucocyte count, TIBC, and CRP and ferritin concentrations exhibited higher RIs compared with those in a nonphysically active population. Thirty volunteers (outliers) were removed from the reference population due to blood abn...
Jornal de Pediatria, 2001
Jornal de Pediatria, 2001
Revista Brasileira de Hematologia e Hemoterapia, 2003
Revista Brasileira de Hematologia e Hemoterapia, 2010
Revista Brasileira De Hematologia E Hemoterapia, 2009
Revista Brasileira De Hematologia E Hemoterapia, Jun 1, 2010
Revista Brasileira De Hematologia E Hemoterapia, Jan 6, 2010
American Journal of Hematology, 2005
Although it is almost certain that α+‐thalassemia protects against malaria, the mechanisms for th... more Although it is almost certain that α+‐thalassemia protects against malaria, the mechanisms for that are still unknown. It has been suggested that an increased number of young circulating red blood cells in α+‐thalassemic children, as a result of some degree of ineffective erythropoiesis, could be related to the high frequencies of the α+‐thalassemic allele in malaria endemic areas. Reticulocyte evaluation in this condition, however, has been poorly performed so far. Our objective was to determine the reticulocyte number and maturation degree, in addition to the soluble transferrin receptor and serum erythropoietin levels, in α+‐thalassemia heterozygotes, comparing them with normal α‐genotype controls. One hundred twenty‐one α+‐thalassemia carriers (−α3.7/αα) and 249 controls (αα/αα), all of them with normal serum ferritin levels, were subclassified according to age (1–5, 6–10, 11–15, 16–20, and over 20 years old). Reticulocyte analyzes were carried out by flow cytometry and sTfR and s‐Epo levels determined by immunonephelometry and chemiluminescence, respectively. The comparisons did not show any significant difference between thalassemics and controls regarding the reticulocyte parameters [percentages and absolute values, P = 0.2643 and 0.5421; high, medium, and low maturation degree, P = 0.2579, 0.2196, and 0.4192; RET maturity index (RMI), P = 0.2471, respectively], as well as the s‐Epo levels (P = 0.5711). The sTfR concentrations were higher in the thalassemic group (P = 0.0001), but statistical significance was due only to the 1–5 and over 20 subgroups (P = 0.0082 and 0.0436, respectively). The results found here are compatible with a compensated erythropoiesis and do not confirm the hypothesis mentioned above. Am. J. Hematol. 81:68–70, 2006. © 2005 Wiley‐Liss, Inc.
Revista Brasileira De Hematologia E Hemoterapia, Oct 1, 2008
Revista Brasileira De Hematologia E Hemoterapia, Oct 1, 2008
Revista Brasileira De Hematologia E Hemoterapia, 2009
Acta Haematologica, 1992
Clinical, laboratory features and restriction enzyme DNA analysis are reported for a black Brazil... more Clinical, laboratory features and restriction enzyme DNA analysis are reported for a black Brazilian woman with HbH disease. The patient presented a thalassemic blood picture with HbH and Hb Bart’s. Gene mapping demonstrated the compound heterozygous state for the --MED and -α3.7 deletions.Copyright © 1992 S. Karger AG, Basel
Journal of Clinical Laboratory Analysis, 2006
Revista Brasileira de Hematologia e Hemoterapia, 2016
Revista Brasileira de Hematologia e Hemoterapia, 2009
Revista Brasileira de Hematologia e Hemoterapia, 2008
Jornal Brasileiro de Patologia e Medicina Laboratorial, 2002
BioMed Research International, 2014
The aim of this study was to establish reference intervals (RIs) for the hemogram and iron status... more The aim of this study was to establish reference intervals (RIs) for the hemogram and iron status biomarkers in a physically active population. The study population included male volunteers (n=150) with an average age of 19 ± 1 years who had participated in a regular and controlled exercise program for four months. Blood samples were collected to determine hematological parameters using a Sysmex XE-5000 analyzer (Sysmex, Kobe, Japan). Iron, total iron-binding capacity (TIBC), transferrin saturation and ferritin, and high-sensitivity C-reactive protein (CRP) concentrations in serum samples were measured using commercial kits (Roche Diagnostics, GmbH, Mannheim, Germany) and a Roche/Hitachi 902 analyzer. The RIs were established using the RefVal program 4.1b. The leucocyte count, TIBC, and CRP and ferritin concentrations exhibited higher RIs compared with those in a nonphysically active population. Thirty volunteers (outliers) were removed from the reference population due to blood abn...
Jornal de Pediatria, 2001
Jornal de Pediatria, 2001
Revista Brasileira de Hematologia e Hemoterapia, 2003
Revista Brasileira de Hematologia e Hemoterapia, 2010