A prospective surveillance study in haemophilia B patients following a population switch to recombinant factor IX (nonacog gamma)
Haemophilia
.
2021 Jul;27(4):e530-e533.
doi: 10.1111/hae.14273.
Epub 2021 Feb 8.
Authors
Evemie Dubé
1
,
Clémence Merlen
1
,
Arnaud Bonnefoy
1
,
Julie Gauthier
2
3
,
Jean-François Castilloux
4
,
Stéphanie Cloutier
5
,
Christine Demers
5
,
Christine A Sabapathy
6
,
Jean St-Louis
1
7
,
Catherine Vézina
6
,
Margaret Warner
6
,
Georges-Étienne Rivard
1
Affiliations
1
Division of Hematology-Oncology, Department of Pediatrics, CHU Sainte-Justine, Montréal, QC, Canada.
2
Molecular Diagnostic Laboratory, CHU Sainte-Justine, Montréal, QC, Canada.
3
Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montréal, QC, Canada.
4
Centre Hospitalier Universitaire de Sherbrooke, Université Sherbrooke, Sherbrooke, QC, Canada.
5
Hôpital de l'Enfant Jésus, CHU de Québec, Québec, QC, Canada.
6
Montreal Children's Hospital, McGill University Health Center, Montréal, QC, Canada.
7
Hôpital Maisonneuve-Rosemont, Montréal, QC, Canada.
PMID:
33555068
DOI:
10.1111/hae.14273
No abstract available
Publication types
Letter
MeSH terms
Factor IX*
Half-Life
Hemophilia B*
Humans
Prospective Studies
Recombinant Proteins
Substances
Recombinant Proteins
Factor IX
Grants and funding
Bayer Canada, grant for Center of Excellence in Haemostasis