Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sandra Stella Lazarte"'
Autor:
Sandra Stella Lazarte, María Eugenia Mónaco, Cecilia Laura Jimenez, Miryam Emilse Ledesma Achem, Magdalena María Terán, Blanca Alicia Issé
Publikováno v:
Advances in Hematology, Vol 2015 (2015)
Most common microcytic hypochromic anemias are iron deficiency anemia (IDA) and β-thalassemia trait (BTT), in which oxidative stress (OxS) has an essential role. Catalase causes detoxification of H2O2 in cells, and it is an indispensable antioxidant
Externí odkaz:
https://doaj.org/article/4fc86ef752724ca889591aca7505683e
Autor:
Sandra Stella Lazarte, María Eugenia Mónaco, Magdalena María Terán, Ana Cecilia Haro, Miryam Emilse Ledesma Achem, Blanca Alicia Issé
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 39, Iss 2, Pp 115-121
ABSTRACT Background: Oxidative stress may aggravate symptoms of hemolytic anemias such as beta-thalassemia. FoxO3 activation results in resistance to oxidative stress in fibroblasts and neuronal cell cultures. Objective: The purpose of this research
Externí odkaz:
https://doaj.org/article/fabb26c12f9a42b9819d2cab863828ce
Publikováno v:
High Altitude Medicine & Biology.
Armella, Flavia Noelia, and Sandra Stella Lazarte. Hematological reference values according to geographical region in Jujuy, Argentina.
Autor:
Magdalena María Terán, Cecilia Haro, Maria Eugenia Monaco, Blanca Issé, Natalia A Asensio, Sandra Stella Lazarte, Emilse Ledesma Achem
Publikováno v:
Hemoglobin. 44:122-127
β-Thalassemia (β-thal) trait is a heterogeneous group of genetic defects leading to decreased β-globin production, ineffective erythropoiesis, and oxidative stress. The aim is to evaluate the cytoprotective response, at transcriptional and systemi
Autor:
Blanca Issé, Myriam E. Ledesma Achem, Sandra Stella Lazarte, Ana Cecilia Haro, Maria Eugenia Monaco, Cecilia Jiménez
Publikováno v:
Hemoglobin. 38:394-401
The main hereditary hemoglobin (Hb) disorder in Argentina is b-thalassemia (b-thal). Molecular studies performed in the center of the country exhibited a marked prevalence of the codon 39 (C4T) and IVS-I-110 (G4A) mutations. The northwest region of A
Autor:
Ledesma Achem Miryam Emilse, Terán Magdalena María, Mónaco María Eugenia, Issé Blanca Alicia, Haro Cecilia, Sandra Stella Lazarte
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Blood research
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Blood research
Background: Hereditary spherocytosis (HS) is a chronic hemolytic anemia characterized by microspherocytes in the peripheral blood and increased erythrocyte osmotic fragility (EOF). This study evaluated the cryohemolysis test (CHT); initial hemolysis
Autor:
Magdalena María Terán, Miryam Emilse Ledesma Achem, Cecilia Jiménez, Blanca Issé, Sandra Stella Lazarte, Maria Eugenia Monaco
Publikováno v:
Advances in Hematology
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Advances in Hematology, Vol 2015 (2015)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Advances in Hematology, Vol 2015 (2015)
Most common microcytic hypochromic anemias are iron deficiency anemia (IDA) and β-thalassemia trait (BTT), in which oxidative stress (OxS) has an essential role. Catalase causes detoxification of H2O2 in cells, and it is an indispensable antioxidant