Zobrazeno 1 - 10
of 48
pro vyhledávání: '"A M, Stain"'
Autor:
Greig Blamey, Elizabeth Sagermann, Alfonso Iorio, A. M. Stain, Linda Waterhouse, Becky Van Tassel
Publikováno v:
Haemophilia. 28:36-41
Introduction The Haemophilia Experiences, Results and Opportunities (HERO) Study identified sexual health as an important psychosocial issue affecting people with haemophilia (PWH) worldwide. However, sexual health is inadequately addressed at haemop
Autor:
Victor S. Blanchette, John K. Wu, Brian M. Feldman, Elizabeth Paradis, Eleanor Pullenayegum, Roona Sinha, Saunya Dover, Nicole Laferriere, Geroges E. Rivard, Anthony K.C. Chan, Daniel Kazandjian, Sara J. Israels, Darius Wrathall, MacGregor Steele, Byron Song, Robert J. Klaassen, Stéphanie Cloutier, Sue Ann Hawes, A. M. Stain
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 4, Iss 2, Pp 318-325 (2020)
Research and Practice in Thrombosis and Haemostasis
Research and Practice in Thrombosis and Haemostasis
Background Standard of care for persons with severe hemophilia A includes regular replacement of factor VIII (FVIII). Prophylaxis regimens using standard half‐life (SHL) FVIII concentrates, while effective, are costly and require frequent intraveno
Autor:
Veerle Labarque, Cecilia Manuel, Victor S. Blanchette, Vanessa Bouskill, Paula D. James, Vanitha Perinparajah, Manuel Carcao, A. M. Stain, David Lillicrap, Cindy Wakefield
Publikováno v:
American Journal of Hematology. 92:E94-E96
Autor:
A. M. Stain, Sölve Elmståhl, Karin Lindvall, Rolf Ljung, Sylvia von Mackensen, Erik Berntorp, Kate Khair
Publikováno v:
Pediatric Blood & Cancer. 61:706-711
Having a child with a chronic disease often increases the burden in the family with more hospital visits, treatment administration, and increased worries for the ill child. A cross-sectional, international, multi-centre study in caregivers of childre
Autor:
A. Cochrane, M. Hang, C. Blanchette, Georgina Floros, A. M. Stain, Victor Blanchette, P. Komvilaisak, Shoshana Revel-Vilk, S. C. Ling, E. A. Roberts
Publikováno v:
Haemophilia. 17:689-694
Summary. Hepatitis in children with haemophilia was historically most often associated with transfusion-transmitted infections. However, with the use of recombinant clotting factor concentrates, acquisition of such infections has now become rare. We
Publikováno v:
Haemophilia. 16:943-948
Summary. Type 3 Von Willebrand disease (VWD) is a rare, severe, autosomal recessive bleeding disorder. In our institution, we follow 17 children with type 3 VWD. We have observed a high prevalence of dental disease in these patients prompting us to u
Publikováno v:
Haemophilia. 14:188-195
Surgery in infants and young children with haemophilia, when preceded by accurate diagnosis and accompanied by safe and effective factor prophylaxis, is not associated with a significant risk of haemorrhage. Haemophilic newborns undergoing circumcisi
Autor:
C. Traivaree, D. Armstrong, Manuel Carcao, Georgina Floros, A. M. Stain, Victor S. Blanchette
Publikováno v:
Haemophilia. 13:552-559
Summary. We conducted a review of a single institutional experience of patients with haemophilia presenting with suspected intracranial haemorrhage (ICH) who underwent computed tomographic (CT) neuro-imaging. We found that over a 9-year period (1996
Autor:
David Lillicrap, Victor S. Blanchette, Manuel Carcao, Kenneth G. Mann, Jayne Leggo, C. Barnes, P. Hilliard, A. M. Stain
Publikováno v:
Haemophilia. 13:202-205
Summary. Although many patients with haemophilia may have exactly the same residual clotting factor level, the clinical disease phenotype may vary greatly. This variation may be related to different genetic mutations responsible for haemophilia, envi
Autor:
Sue Ann Hawes, A. M. Stain, Man-Chiu Poon, Anthony K.C. Chan, Georges-Etienne Rivard, A. R. Langley, Stéphanie Cloutier, S. Chait, Robert J. Klaassen, R. Card, John K. Wu, Victor S. Blanchette, Nicole Laferriere, M. Mclimont, Brian M. Feldman, Sara J. Israels
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 21(4)
Introduction Haemophilia A treatment with factor VIII concentrates requires frequent venipunctures; a central venous access device (CVAD) may be required to facilitate reliable venous access, especially in young children. While CVADs provide reliable