Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Karen Charpentier"'
Autor:
Ali Amid, Shiyi Chen, Uma Athale, Karen Charpentier, Manuela Merelles-Pulcini, Isaac Odame, Melanie Kirby-Allen
Publikováno v:
Haematologica, Vol 103, Iss 5 (2018)
Externí odkaz:
https://doaj.org/article/80d73b1d60ab4206ae49ca94c2e63b99
Outcomes of haemoglobin Bart’s hydrops fetalis following intrauterine transfusion in Ontario, Canada
Autor:
Laura Janzen, Shiyi Chen, Melanie Kirby-Allen, John S. Waye, Gareth Seaward, Karen Charpentier, Uma H. Athale, Catherine I. Segbefia, Greg Ryan, Ali Amid, Hui Jue Zhang, Edmond Kelly, Isaac Odame, Manuela Merelles-Pulcini
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 106:51-56
ObjectivesWith improved access to intrauterine transfusion (IUT), more fetuses with haemoglobin Bart’s hydrops fetalis (HBHF; homozygous α0-thalassaemia) will survive.DesignTo evaluate the long-term outcome of affected fetuses with and without IUT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::431784ab68290a85e7e3865b91843360
https://doi.org/10.1136/archdischild-2019-317626
https://doi.org/10.1136/archdischild-2019-317626
Autor:
Paul Monagle, Karen Charpentier, M. Patricia Massicotte, David Dix, Suzanne Bridge, Velma Marzinotto, Michael Leaker, Gabrielle deVeber, Maureen Andrew, Anthony K.C. Chan
Publikováno v:
The Journal of Pediatrics. 136:439-445
Objective: Low molecular weight heparins (LMWHs) offer several advantages over standard anticoagulant therapy (unfractionated heparin/warfarin) including predictable pharmacokinetics, minimal monitoring, and subcutaneous administration. Our objective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2845abddf4890e4cf77eaabd1ffe840d
https://doi.org/10.1016/s0022-3476(00)90005-2
https://doi.org/10.1016/s0022-3476(00)90005-2
Publikováno v:
Pediatric bloodcancer. 52(4)
Aplastic anemia (AA) is a rare disorder in children, usually treated with immunosuppressive therapy (IST) including antithymocyte globulin (ATG) and cyclosporin A. There are no current widely used alternative therapies with comparable efficacy. We de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a8871163cb4afce94b8be3d7086c10a
https://pubmed.ncbi.nlm.nih.gov/19058202
https://pubmed.ncbi.nlm.nih.gov/19058202
Autor:
Jeffrey H. Lipton, Lawrence Jardine, Yvan Samson, Yigal Dror, Derek Stephens, Josette Champagne, Rochelle Yanofsky, Sharon Abish, Kaiser Ali, J.M. Steele, Karen Charpentier, Josee Brossard, Lillian Sung, John K. Wu, Melvin H. Freedman, J.P. Hand, Robert J. Klaassen, M. Silva, Conrad V. Fernandez, Isaac Odame, D. Le
Publikováno v:
Pediatric bloodcancer. 47(7)
Background:. Inherited bone marrow failure syndromes (IMFSs) are genetic disorders characterized by defective single-lineage or multi-lineage hematopoiesis. IMFS patients are at risk for severe cytopenias, development of marrow cytogenetic abnormalit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb0d3563a3be28ae8a89eb30629c8147
https://pubmed.ncbi.nlm.nih.gov/16676307
https://pubmed.ncbi.nlm.nih.gov/16676307