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Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 11, 2006
Quality of life assessment in clinical practice in haemophilia treatment
A Gringeri, L Mantovani, S V Mackensen
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
May 16, 2008
[Quality of life of young patients with haemophilia in Europe]
Monika Bullinger, A Gringeri, S von Mackensen
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
July 2, 2010
Special lectures in haemophilia management
A Batorova, K A High, A Gringeri
La Ricerca in Clinica E in Laboratorio
|
October 1, 1990
High-purity factor VIII concentrates produced without using monoclonal antibodies
P M Mannucci, A Gringeri, M Cattaneo
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 30, 2012
Tertiary prophylaxis in adults: is there a rationale?
A Gringeri, T Lambert, A Street, et al.
Cancer Research
|
October 15, 1988
Diethyldithiocarbamate inhibition of murine bone marrow toxicity caused by cis-diamminedichloroplatinum(II) or diammine-(1,1-cyclobutanedicarboxylato)platinum(II)
A Gringeri, P C Keng, R F Borch
Thrombosis and Haemostasis
|
August 1, 1995
Inhibitors to factor VIII in a family with mild hemophilia: molecular characterization and response to factor VIII and desmopressin
E Santagostino, A Gringeri, L Tagliavacca, et al.
British Journal of Haematology
|
March 1, 1992
Intramuscular anti-D immunoglobulins for home treatment of chronic immune thrombocytopenic purpura
A Gringeri, M Cattaneo, E Santagostino, et al.
American Journal of Hematology
|
August 1, 1984
Abnormalities of lymphocyte subsets are correlated with concentrate consumption in asymptomatic Italian hemophiliacs treated with concentrates made from American plasma
P M Mannucci, A Gringeri, M Ammassari, et al.
British Journal of Haematology
|
February 1, 1994
Patients with severe von Willebrand disease are insensitive to the releasing effect of DDAVP: evidence that the DDAVP-induced increase in plasma factor VIII is not secondary to the increase in plasma von Willebrand factor
M Cattaneo, L Simoni, A Gringeri, et al.
Page
of 13
Search research articles
Search
Showing results (11-20 of 122) with videos related to
Sort By:
Page
of 13
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 11, 2006
Quality of life assessment in clinical practice in haemophilia treatment
A Gringeri, L Mantovani, S V Mackensen
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
May 16, 2008
[Quality of life of young patients with haemophilia in Europe]
Monika Bullinger, A Gringeri, S von Mackensen
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
July 2, 2010
Special lectures in haemophilia management
A Batorova, K A High, A Gringeri
La Ricerca in Clinica E in Laboratorio
|
October 1, 1990
High-purity factor VIII concentrates produced without using monoclonal antibodies
P M Mannucci, A Gringeri, M Cattaneo
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 30, 2012
Tertiary prophylaxis in adults: is there a rationale?
A Gringeri, T Lambert, A Street, et al.
Cancer Research
|
October 15, 1988
Diethyldithiocarbamate inhibition of murine bone marrow toxicity caused by cis-diamminedichloroplatinum(II) or diammine-(1,1-cyclobutanedicarboxylato)platinum(II)
A Gringeri, P C Keng, R F Borch
Thrombosis and Haemostasis
|
August 1, 1995
Inhibitors to factor VIII in a family with mild hemophilia: molecular characterization and response to factor VIII and desmopressin
E Santagostino, A Gringeri, L Tagliavacca, et al.
British Journal of Haematology
|
March 1, 1992
Intramuscular anti-D immunoglobulins for home treatment of chronic immune thrombocytopenic purpura
A Gringeri, M Cattaneo, E Santagostino, et al.
American Journal of Hematology
|
August 1, 1984
Abnormalities of lymphocyte subsets are correlated with concentrate consumption in asymptomatic Italian hemophiliacs treated with concentrates made from American plasma
P M Mannucci, A Gringeri, M Ammassari, et al.
British Journal of Haematology
|
February 1, 1994
Patients with severe von Willebrand disease are insensitive to the releasing effect of DDAVP: evidence that the DDAVP-induced increase in plasma factor VIII is not secondary to the increase in plasma von Willebrand factor
M Cattaneo, L Simoni, A Gringeri, et al.
Page
of 13