Zobrazeno 1 - 10
of 31
pro vyhledávání: '"E. Agriello"'
Autor:
Evangelina González, Sofía Grille, Valeria Vales, Matilde Boada, Lorena M. Zanella, Daniel Leal, Nehuen P. Gasparini, Cecilia Guillermo, Evangelina E. Agriello, Mariana Stevenazzi, Daniela Lens
Publikováno v:
Revista Médica del Uruguay, Vol 32, Iss 3, Pp 145-151 (2016)
Introducción: en los últimos años ha existido un avance significativo en el conocimiento biológico de la leucemia aguda mieloide (LAM) que se ha traducido en que el tratamiento de los pacientes afectados se realice guiado por el perfil citogenét
Externí odkaz:
https://doaj.org/article/2a2f90f2bb644e54af6accfbcc1beeb8
Autor:
Davi Coe Torres, Miguel A. Pavlovsky, Irma Slavutsky, Claudia Ortega, Lorena Zanella, Carmen Stanganelli, Raimundo F. Bezares, María Elena Márquez, Evangelina E. Agriello, Claudia Mardaraz, Cecilia Lang, Pablo Oppezzo, Camila Galvano, Juana Cabrera, Andrea Krzywinski, Victoria Remedi, Astrid Pavlovsky
Publikováno v:
Annals of Hematology. 101:341-348
Chronic lymphocytic leukemia (CLL) is the most common mature B-cell neoplasm in the West. IGHV4-34 is one of the most frequently used genes in CLL patients, which usually display an indolent outcome. In this study, we explored the mutational profile
Autor:
M. Lincango, V. Andreoli, H. Garcia Rivello, M. Asinari, A. Bender, C. Alfero, A. Catalán, M. Rahhal, R. Delamer, M.J. Mela Osorio, A. Navickas, S. Grille, E. Agriello, M. Castro, M.A. Perusini, J. Arbelbide, A. Basquiera, C. Belli
Publikováno v:
Leukemia Research. 128:107144
Autor:
Carmen Stanganelli, PV Campregher, Andrea Krzywinski, Raul Gabus, Adriano de Paula Sabino, Caio Perez Gomes, Priscilla Segges, Davi Coe Torres, Celso Arrais Rodrigues, Mihoko Yamamoto, María Lourdes Lopes Ferrari deChauffaille, Claudia Ortega, Camila Galvano, Rocio Hassan, Lorena Zanella, María Cabrejo, Eliana Abdelhay, Pierre-Antoine Deglesne, José Luis López, María Elena Márquez, Guillermo Dighiero, Cecilia Lang, Raimundo F. Bezares, Pablo Oppezzo, Juana Cabrera, Natalia Sotelo, Ricardo Bigni, Irma Slavutsky, Evangelina E. Agriello, Maria Tereza Cartaxo Muniz
Publikováno v:
Hematological Oncology. 37:644-648
Autor:
Nehuen P. Gasparini, Evangelina E. Agriello, M. J. Lorena Zanella, María P. Iommi, Juan Maradei, Marisa J. Sandoval
Publikováno v:
Medicina (Buenos Aires), Vol 76, Iss 6, Pp 369-372 (2016)
Sickle cell syndrome HbS/β thalassemia is an inheritable mendelian type disease where two affected alleles are simultaneously present, one from HbS (βS) and the other from β thalassemia. That situation is mainly linked to individuals who share Afr
Autor:
S. Garbiero, E. Tania, M. Brandt, G. Taborda, B. Pertine, M. Sandoval, P. Iommi, F. Torreguitart, O. Gómez, E. Agriello, M. Beccacece, J. Maradei
Publikováno v:
HemaSphere. 3:949
Autor:
Gómez Pasanante, E. Etchepareborda, Verónica E. García, E. Agriello, Leonardo Fainboim, M. Irigoyen, Rosanna Ramhorst, Adriana Corigliano
Publikováno v:
American Journal of Reproductive Immunology. 49:149-158
PROBLEM: To characterize in fertile women and women with recurrent spontaneous abortions (RSA) the expression and functional status of T cells expressing the CD69 molecule. METHOD OF STUDY: We analyzed by flow cytometry in peripheral blood and endome
Autor:
Sandra Zittermann, Bibiana I. Achino, Leonardo Fainboim, Rosanna Ramhorst, Evangelina E. Agriello, Nora Silvia Halperin
Publikováno v:
European Journal of Haematology. 66:377-382
CD44 expression and other B cell markers were analyzed in 38 samples of B cell precursors (BCP) from patients with acute lymphoblastic leukemia (ALL). According to the expression of CD10 and CD44, we established the following five stages of BCP-ALL p
Autor:
M. Cortelezzi, Leonardo Fainboim, Eduardo Lombardi, C. Contreras Ortiz, J.J. Etchepareborda, M. Pando, M. Irigoyen, L. Auge, Sandra Zittermann, E. Agriello, Rosanna Ramhorst, J. Larriba
Publikováno v:
American Journal of Reproductive Immunology. 44:129-135
PROBLEM: Alloimmunization as a treatment for recurrent spontaneous abortion (RSA) is still controversial due to the lack of enough controls to evaluate its effectiveness. The present study was conducted to compare the live birth rate in the presence
Publikováno v:
Journal of inherited metabolic disease. 32
Fabry disease is an X-linked lysosomal storage disorder of glycosphingolipid catabolism due to the deficient activity of the enzyme alpha-galactosidase A. The non-degraded substrate, mainly globotriaosylceramide (Galα1-4Galβ1-4Glcβ1-1Cer; Gb(3)) a