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Journal of Veterinary Medicine. B, Infectious Diseases and Veterinary Public Health
|
May 11, 2002
Diagnosis of Mycobacterium bovis infection in calves sensitized by mycobacteria of the avium/intracellulare group
M Amadori, S Tagliabue, S Lauzi, et al.
Dermatology (Basel, Switzerland)
|
January 1, 1992
Antiphospholipid antibodies and melanoma: a link?
L Naldi, G Finazzi, A Brevi, et al.
European Journal of Haematology
|
August 1, 1990
Low incidence of bleeding from HIV-related thrombocytopenia in drug addicts and hemophiliacs: implications for therapeutic strategies
G Finazzi, P M Mannucci, A Lazzarin, et al.
Thrombosis and Haemostasis
|
April 1, 1995
Apparent heterozygous type II protein C deficiency caused by the factor V 506 Arg to Gln mutation
H Ireland, T Bayston, E Thompson, et al.
The New England Journal of Medicine
|
December 20, 1997
The threshold for prophylactic platelet transfusions in adults with acute myeloid leukemia. Gruppo Italiano Malattie Ematologiche Maligne dell'Adulto
P Rebulla, G Finazzi, F Marangoni, et al.
Blood
|
September 1, 1984
Studies of the pathophysiology of acquired von Willebrand's disease in seven patients with lymphoproliferative disorders or benign monoclonal gammopathies
P M Mannucci, R Lombardi, R Bader, et al.
Annals of the Rheumatic Diseases
|
March 1, 1993
Cutaneous manifestations associated with antiphospholipid antibodies in patients with suspected primary antiphospholipid syndrome: a case-control study
L Naldi, F Locati, L Marchesi, et al.
Haematologica
|
May 9, 2000
Diagnosis of essential thrombocythemia at platelet counts between 400 and 600x10(9)/L. Gruppo Italiano Malattie Mieloproliferative Croniche(GIMMC)
S Sacchi, G Vinci, L Gugliotta, et al.
Thrombosis Research
|
December 1, 1991
A common point mutation producing type 1A antithrombin III deficiency: AT129 CGA to TGA (Arg to Stop)
R J Olds, D A Lane, H Ireland, et al.
Blood
|
November 11, 1999
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)
E M Faioni, F Franchi, P Bucciarelli, et al.
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Search research articles
Search
Showing results (91-100 of 132) with videos related to
Sort By:
Page
of 14
Journal of Veterinary Medicine. B, Infectious Diseases and Veterinary Public Health
|
May 11, 2002
Diagnosis of Mycobacterium bovis infection in calves sensitized by mycobacteria of the avium/intracellulare group
M Amadori, S Tagliabue, S Lauzi, et al.
Dermatology (Basel, Switzerland)
|
January 1, 1992
Antiphospholipid antibodies and melanoma: a link?
L Naldi, G Finazzi, A Brevi, et al.
European Journal of Haematology
|
August 1, 1990
Low incidence of bleeding from HIV-related thrombocytopenia in drug addicts and hemophiliacs: implications for therapeutic strategies
G Finazzi, P M Mannucci, A Lazzarin, et al.
Thrombosis and Haemostasis
|
April 1, 1995
Apparent heterozygous type II protein C deficiency caused by the factor V 506 Arg to Gln mutation
H Ireland, T Bayston, E Thompson, et al.
The New England Journal of Medicine
|
December 20, 1997
The threshold for prophylactic platelet transfusions in adults with acute myeloid leukemia. Gruppo Italiano Malattie Ematologiche Maligne dell'Adulto
P Rebulla, G Finazzi, F Marangoni, et al.
Blood
|
September 1, 1984
Studies of the pathophysiology of acquired von Willebrand's disease in seven patients with lymphoproliferative disorders or benign monoclonal gammopathies
P M Mannucci, R Lombardi, R Bader, et al.
Annals of the Rheumatic Diseases
|
March 1, 1993
Cutaneous manifestations associated with antiphospholipid antibodies in patients with suspected primary antiphospholipid syndrome: a case-control study
L Naldi, F Locati, L Marchesi, et al.
Haematologica
|
May 9, 2000
Diagnosis of essential thrombocythemia at platelet counts between 400 and 600x10(9)/L. Gruppo Italiano Malattie Mieloproliferative Croniche(GIMMC)
S Sacchi, G Vinci, L Gugliotta, et al.
Thrombosis Research
|
December 1, 1991
A common point mutation producing type 1A antithrombin III deficiency: AT129 CGA to TGA (Arg to Stop)
R J Olds, D A Lane, H Ireland, et al.
Blood
|
November 11, 1999
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)
E M Faioni, F Franchi, P Bucciarelli, et al.
Page
of 14