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Journal of Pediatric Hematology/Oncology
|
April 25, 2000
Low-molecular-weight heparin in thrombotic disease in children and adolescents
R C Punzalan, C A Hillery, R R Montgomery, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 9, 2011
Exposure and safety of higher doses of recombinant factor VIIa ≥250 μg kg(-1) in individuals with congenital haemophilia complicated by alloantibody inhibitors: the Haemophilia and Thrombosis Research Society Registry experience (2004-2008)
E J Neufeld, C M Kessler, J C Gill, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 14, 2004
Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrate (Humate-P)
A R Thompson, J C Gill, B M Ewenstein, et al.
Nephron
|
January 1, 1994
Increased incidence of HLA-B40 group antigens in children with hemolytic-uremic syndrome
K J Sheth, J C Gill, H E Leichter, et al.
Blood
|
June 1, 1987
The effect of ABO blood group on the diagnosis of von Willebrand disease
J C Gill, J Endres-Brooks, P J Bauer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 4, 2011
von Willebrand factor/factor VIII concentrate (Humate-P) for management of elective surgery in adults and children with von Willebrand disease
J C Gill, A Shapiro, L A Valentino, et al.
Blood
|
October 1, 1996
Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets
D J Mancuso, P A Kroner, P A Christopherson, et al.
The Journal of Pediatrics
|
June 8, 2001
Bleeding disorders: A common cause of menorrhagia in adolescents
J A Bevan, K W Maloney, C A Hillery, et al.
Thrombosis and Haemostasis
|
June 24, 1985
Persistence and progression of immunologic abnormalities in haemophilia
J C Gill, D Wheeler, J E Menitove, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 30, 2018
Risk factors associated with invasive orthopaedic interventions in males with haemophilia enrolled in the Universal Data Collection program from 2000 to 2010
P Tobase, H Lane, A-E-A Siddiqi, et al.
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of 8
Search research articles
Search
Showing results (41-50 of 72) with videos related to
Sort By:
Page
of 8
Journal of Pediatric Hematology/Oncology
|
April 25, 2000
Low-molecular-weight heparin in thrombotic disease in children and adolescents
R C Punzalan, C A Hillery, R R Montgomery, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 9, 2011
Exposure and safety of higher doses of recombinant factor VIIa ≥250 μg kg(-1) in individuals with congenital haemophilia complicated by alloantibody inhibitors: the Haemophilia and Thrombosis Research Society Registry experience (2004-2008)
E J Neufeld, C M Kessler, J C Gill, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 14, 2004
Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrate (Humate-P)
A R Thompson, J C Gill, B M Ewenstein, et al.
Nephron
|
January 1, 1994
Increased incidence of HLA-B40 group antigens in children with hemolytic-uremic syndrome
K J Sheth, J C Gill, H E Leichter, et al.
Blood
|
June 1, 1987
The effect of ABO blood group on the diagnosis of von Willebrand disease
J C Gill, J Endres-Brooks, P J Bauer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 4, 2011
von Willebrand factor/factor VIII concentrate (Humate-P) for management of elective surgery in adults and children with von Willebrand disease
J C Gill, A Shapiro, L A Valentino, et al.
Blood
|
October 1, 1996
Type 2M:Milwaukee-1 von Willebrand disease: an in-frame deletion in the Cys509-Cys695 loop of the von Willebrand factor A1 domain causes deficient binding of von Willebrand factor to platelets
D J Mancuso, P A Kroner, P A Christopherson, et al.
The Journal of Pediatrics
|
June 8, 2001
Bleeding disorders: A common cause of menorrhagia in adolescents
J A Bevan, K W Maloney, C A Hillery, et al.
Thrombosis and Haemostasis
|
June 24, 1985
Persistence and progression of immunologic abnormalities in haemophilia
J C Gill, D Wheeler, J E Menitove, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 30, 2018
Risk factors associated with invasive orthopaedic interventions in males with haemophilia enrolled in the Universal Data Collection program from 2000 to 2010
P Tobase, H Lane, A-E-A Siddiqi, et al.
Page
of 8