Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Silvia Montilla"'
Autor:
Rebeca Ibarra-Hernández, Sergio Sánchez-Sosa, Javier Cervantes-Bojalil, Silvia Montilla-Fonseca, Carolina Cruz-Reyes, Ismael Íñiguez-Galo, Sergio Sánchez-Barrera, Jesús Vizcarra, Iván González
Publikováno v:
Journal of Clinical Oncology. 36:e24025-e24025
e24025Background: We conducted this study to describe and assess liquid biopsy’s clinical usefulness in the identification of predictive response biomarkers in patients with advanced cancer. Method...
Autor:
Nathalie Gérard, Anabel Arends, Odalis García, Omar Castillo, Gilberto Gómez, Martha Bravo-Urquiola, Tsouria Berbar, Gloria García, Marycarmen Chacín, Dalia Velasquez, Rajagopal Krishnamoorthy, Silvia Montilla
Publikováno v:
Hemoglobin. 36(3)
In order to establish the spectrum of β-thalassemia (β-thal) mutations in the Venezuelan population for the first time, 127 unrelated subjects either with a suspicion of β-thal trait or with a clinically recognized β-thal syndrome of different de
Autor:
Martha, Bravo-Urquiola, Anabel, Arends, Silvia, Montilla, José María, Guevara-I, Gloria, García, Maritza, Alvarez, Omar, Castillo
Publikováno v:
Investigacion clinica. 47(2)
The propositus is a two year old child with a severe hemolytic anemia and increased level of Hb F. The Hbs A, A2 and F were eluted and quantitated by cation exchange high-performance liquid chromatography (HPLC-CE). DNA was isolated from peripheral b
Autor:
Martha, Bravo-Urquiola, Anabel, Arends, Silvia, Montilla, Dalia, Velásquez, Gloria, Garcìa, Maritza, Alvarez, José, Guevara, Omar, Castillo
Publikováno v:
Investigacion clinica. 45(4)
The hemoglobinopathies are a very heterogeneous group of congenital hemolytic anemias, which includes hemoglobin (Hb) variants, thalassemia and hereditary persistence of fetal hemoglobin (HPFH). The aim of this study was to determine the frequency of
Autor:
martha Bravo Urquiola, L Dalia Velásquez De, Natalie Gerard, Gloria García Lic, Rajagapol Krishnamoorthy, Silvia Montilla, Anabel Arends, Maritza Alvarez
Publikováno v:
Blood. 104:3728-3728
Hereditary Persistence of Fetal Hemoglobin (HPFH) is a clinically benign condition characterized by continuous synthesis of fetal hemoglobin (Hb F) in adult life without major related hematological changes. The nondeletional HPFH is characterized by
Autor:
Bravo-Urquiola, Martha1 (AUTHOR), Arends, Anabel1 (AUTHOR) aarends@cantv.net, Gómez, Gilberto1 (AUTHOR), Montilla, Silvia1 (AUTHOR), Gerard, Nathalie2 (AUTHOR), Chacin, Marycarmen1 (AUTHOR), Berbar, Tsouria2 (AUTHOR), García, Odalis1 (AUTHOR), García, Gloria1 (AUTHOR), Velasquez, Dalia1 (AUTHOR), Castillo, Omar3 (AUTHOR), Krishnamoorthy, Rajagopal2 (AUTHOR)
Publikováno v:
Hemoglobin. Jun2012, Vol. 36 Issue 3, p209-218. 10p.