Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Analia Sanchez‐Luceros"'
Autor:
Predrag Miljic, Abdelrahman Noureldin, Michelle Lavin, Sajida Kazi, Analia Sanchez-Luceros, Paula D. James, Maha Othman
Publikováno v:
Journal of Thrombosis and Haemostasis. 21:154-163
Autor:
Célia Dos Santos, Santiago Castera, José Fernandez, Julieta Soledad Rosales, Franco Crescitelli, Santiago Boughen, Marcelo Iastrebner, Osvaldo Guerrero, Carlos Amell Menco, Mariela Gomez, Jacqueline Gonzalez, Maria Fabiana Alberto, Analía Sanchez-Luceros
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 4, Pp 511-515 (2024)
Externí odkaz:
https://doaj.org/article/a1be18641c034be8bc98aff0c29c876f
Von Willebrand disease type 2M: Correlation between genotype and phenotype: Comment from Woods et al
Autor:
Adriana I. Woods, Juvenal Paiva, Debora M. Primrose, Alicia N. Blanco, Analia Sanchez‐Luceros
Publikováno v:
Journal of Thrombosis and Haemostasis. 20:1022-1023
Autor:
Célia Dos Santos, Jesica Trinidad, Santiago Castera, Laura Alconcher, Paula Alejandra Coccia, Federico Javier Manni, María Fabiana Alberto, Analía Sánchez-Luceros
Publikováno v:
Exploration of Immunology, Vol 3, Iss 6, Pp 513-524 (2023)
Aim: To describe the clinical characteristics and frequency of anti-factor H (FH) autoantibody-associated atypical hemolytic uremic syndrome (aHUS) in the first cohort of Argentine patients. Methods: The presence of anti-FH autoantibodies in 70 pedia
Externí odkaz:
https://doaj.org/article/ec4a62bdef09433b952b7998997732d8
Autor:
Célia Dos Santos, Juvenal Paiva, María Lucila Romero, Mara Agazzoni, Ana Catalina Kempfer, Sabrina Rotondo, María Marta Casinelli, María Fabiana Alberto, Analía Sánchez‐Luceros
Publikováno v:
eJHaem, Vol 2, Iss 2, Pp 149-156 (2021)
Abstract Introduction Introduction: Thrombotic microangiopathies (TMAs) are rare disorders associated with fatal outcomes if left uncared for. However, healthcare problems in developing countries tend to limit medical assistance to patients. Methods
Externí odkaz:
https://doaj.org/article/5c89136facd644a0964cd9b1a60d206b
Akademický článek
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Autor:
Analía Sánchez-Luceros, Adriana I. Woods, Emilse Bermejo, Shilpa Shukla, Suchitra Acharya, Michelle Lavin, Natalia Rydz, Maha Othman
Publikováno v:
Platelets, Vol 28, Iss 5, Pp 484-490 (2017)
Despite the increased worldwide awareness, over the last decade, of the platelet-type von Willebrand Disease (PT-VWD), many uncertainties remain around this rare platelet bleeding disorder. This report aims to correctly identify and study the phenoty
Externí odkaz:
https://doaj.org/article/2ee8464533f5442cbbdcc252fe76142c
Autor:
Analia Sanchez-Luceros, Meschengieser, S. S., Woods, A. I., Blanco, A. N., Kempfer, A. C., Casais, P., Salviú, M. J., Lazzari, M. A.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9be12025f0ac1caeaf5192177c44b2b0
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036199321&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036199321&partnerID=MN8TOARS
Autor:
Emilse Bermejo, Maria F. Alberto, David S. Paul, Aaron A. Cook, Paquita Nurden, Analia Sanchez Luceros, Alan T. Nurden, Wolfgang Bergmeier
Publikováno v:
Platelets, Vol 29, Iss 1, Pp 84-86 (2018)
Congenital platelet function disorders are often the result of defects in critical signal transduction pathways required for platelet adhesion and clot formation. Mutations affecting RASGRP2, the gene encoding the Rap GTPase activator, CalDAG-GEFI, g
Externí odkaz:
https://doaj.org/article/a7b7754dc5cb4cefa0780ee777b732fd