Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Nora Watman"'
Autor:
Barbara C. Soberon, Guillermo I. Drelichman, Nicolas Fernandez Escobar, Nora Basack, Gabriel Aguilar, Maria Silvia Larroude, Adriana E. Rocaspana, Analia G. Carvani, Adriana D.V. Arizó, Sandra R. Borchichi, Maria A. Cedola, Maria F. Cuello, Vanesa Avalos, Blanca Diez, Marta Dragosky, Gustavo L. Kantor, Elsa M. Nucifora, Graciela Pujal, Paola L. Reichel, Adriana N. Degano, Nora Watman, Graciela O. Elena, Norberto Guelbert, Juan J. Chain, Marcela A. Aznar
Publikováno v:
Molecular Genetics and Metabolism. 138:107323
Autor:
Karen G. Scheps, Juan Pablo Salim, Viviana Varela, Nora Basack, Eliana García, Renée Crisp, Gustavo Chiappe, Silvia De Paula, Nora Watman, Ana Zerdiew, Héctor M. Targovnik
Publikováno v:
Human Gene. 33:201071
Autor:
Juan Pablo Zarate, Fernando Manzur, Rodolfo D. Cançado, Nora Watman, Fabiola Traina, Guillermo Drelichman, Clarisse Lopes de Castro Lobo, Luis Marfil, Miriam Park, Zulay Chona
Objectives: A multicenter, noninterventional, observational study was conducted in the Latin American countries including Argentina, Brazil, Colombia, Mexico, and Venezuela to assess the prevalence of liver and cardiac iron overload using magnetic re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305e2c83b106ad6d8064834263c4789b
Autor:
Meredith C. Foster, Nadia Belmatoug, Elena Lukina, Manisha Balwani, M. Judith Peterschmitt, Sebastiaan J.M. Gaemers, Derralynn Hughes, Nora Watman, Grace Lewis
Publikováno v:
JIMD Reports
Gaucher disease type 1 (GD1) is an inherited lysosomal storage disorder caused by deficient enzymatic activity of acid β‐glucosidase, resulting in accumulation of its substrate glucosylceramide, leading to debilitating visceral, hematologic, and s
Autor:
Sebastiaan J.M. Gaemers, Nora Watman, Marta Dragosky, Meredith C. Foster, M. Judith Peterschmitt, Elena Lukina, Elsa Avila Arreguin, Ari Zimran, Hanna Rosenbaum, Heather Lau
Publikováno v:
American Journal of Hematology
Eliglustat is a first‐line oral therapy for adults with Gaucher disease type 1 (GD1) and poor, intermediate or extensive CYP2D6‐metabolizer phenotypes (>90% of patients). We report the final results of a Phase 2 trial and extension (NCT00358150)
Autor:
Gabriel Fernández, José Ferro, María Veloso, Marta Dragosky, Nazario Boido, Ramiro Fernández, Liliana Franco, Sandra Zirone, Roberto Albina, Victoria Lanza, Susana S. Meschengieser, Hugo Medici, Nicolás Fernández Escobar, Lucia Barazzutti, Graciela Elena, Andrea Schenone, José Luis Saavedra, Analía Carvani, Greogorio Buchovsky, Luis Aversa, Alejandra Cedola, David Verón, Katja Muller, Nora Watman, Beatriz Girardi, Marcela Corrales, Graciela Galván, Marcelo Contte, Angie Barbieri María, Gabriela Nuñez, Luis Quiroga, Gabriela Aguilar, Alba Ruiz, Julieta Bietti, Marisa Marquez, Lucía Richard, Hugo Robledo, Paola Reichel, Graciela Zárate, Leonardo Feldman, María Fernanda Cuello, Sergio Gómez, Victoria Welsh, Francis Del Río, Mario Savarino, María Á Lvarez Bollea, María Silvia Larroude, Andrés Marino, Marcela Aznar, Moira Bolesina, Cristina Cabral Castella, S Ernesto Veber, Gustavo Kantor, Patricia De Ambrosio, Daniel Bar, Adriana Degano, Alba Sanabria, Viviana Bacciedoni, Norberto Guelbert, Rubén Colimodio, María Nucifora, Marcelo Pujol, Adriana Arizo, Alcyra Fynn, Germán Damiani, Nora Basack, Juan José Chain, Bárbara Soberón, Graciela Pujal, María Brun, Sandra Borchichi, Gisela Nisnovich, Rossana Jaureguiberry, Gustavo Carro, Marina Szlago, Hugo Donato, Alejandra Maro, Ccecilia Baduel, Blanca Diez, María Cristina Rapetti, Isabel Pacheco, Maura Papucci, Guillermo Drelichman, Maya Schweri, Ignacio Fernández
Publikováno v:
American Journal of Hematology. 91:E448-E453
Patients with Gaucher type 1 (GD1) throughout Argentina were enrolled in the Argentine bone project to evaluate bone disease and its determinants. We focused on presence and predictors of bone lesions (BL) and their relationship to therapeutic goals
Autor:
Yestle Kim, Sebastiaan J.M. Gaemers, Mererdith Foster, Manisha Balwani, M. Judith Peterschmitt, Nadia Belmatoug, Elena Lukina, Nora Watman, Derralynn Hughes
Publikováno v:
Molecular Genetics and Metabolism. 126:S27-S28
Autor:
Marcela Cavalcante de Andrade Silva, Carolina Bárbara Belli, Silvia Maria Meira Magalhães, M. Rosenhain, Pedro Negri Aranguren, Yesica Soledad Bestach, Jacqueline Gonzalez, María Soledad Undurraga, Irene Larripa, Ronald Feitosa Pinheiro, Graciela Alfonso, Roberta Sandra da Silva Tanizawa, Ximena Valladares, Elvira Deolinda Rodrigues Pereira Velloso, Nora Watman, Hernán García Rivello
Publikováno v:
American Journal of Hematology. 90:851-858
Fil: Belli, Carolina Barbara. Consejo Nacional de Investigaciones Cientificas y Tecnicas. Instituto de Medicina Experimental. Academia Nacional de Medicina de Buenos Aires. Instituto de Medicina Experimental; Argentina
Autor:
Amal El-Beshlawy, Ana Maria Martins, Renata Cravo, Sebastiaan J.M. Gaemers, M. Judith Peterschmitt, Guillermo Drelichman, Timothy M. Cox, Ozlem Goker-Alpan, Elena Lukina, Barry E. Rosenbloom, Manisha Balwani, Thomas A. Burrow, Regina Tayag, Maria Lucia Alves Pedroso, Priya S. Kishnani, Nora Watman
In the phase 3 Study of Eliglustat Tartrate (Genz-112638) in Patients With Gaucher Disease Who Have Reached Therapeutic Goals With Enzyme Replacement Therapy (ENCORE), at 1 year, eliglustat was noninferior to imiglucerase enzyme therapy in maintainin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e29f459cc07cfd59247d00312a84f24d
Autor:
María Gabriela Flores, Jorge Arbelbide, Irene Larripa, Yesica Soledad Bestach, Virginia Palau Nagore, Carolina Bárbara Belli, Yamila Sieza, Jacqueline Gonzalez, Nora Watman
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Myelodysplastic syndromes (MDS) represent a heterogeneous group of hematologic disorders characterized by cytopenia(s) and predisposition to leukemic progression. An immune dysregulation and an aberrant bone marrow microenvironment seem to be key ele