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Haemostasis
|
January 1, 1989
Congenital factor XIII deficiency with multiple benign breast tumours and successful pregnancy with substitutive therapy. A case report
Z Boda, G Pfliegler, L Muszbek, et al.
Clinical Chemistry
|
August 14, 1998
A microassay to assess the oxidative resistance of low-density lipoproteins
L Ujhelyi, J Balla, L Muszbek, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 28, 2017
Severe bleeding diatheses in an elderly patient with combined type autoantibody against factor XIII A subunit; novel approach to the diagnosis and classification of anti-factor XIII antibodies
M Kun, N Szuber, É Katona, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 29, 2007
A collaborative study to establish the 1st International Standard for factor XIII plasma
S Raut, R E Merton, P Rigsby, et al.
Blood
|
September 26, 2000
Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia
I Balogh, G Szôke, L Kárpáti, et al.
Tissue & Cell
|
January 1, 1987
Identification of smooth muscle-derived foam cells in the atherosclerotic plaque of human aorta with monoclonal antibody IIG10
M A Glukhova, O I Ornatsky, M G Frid, et al.
Annals of Hematology
|
May 15, 2015
Plasma clot properties in patients with a mild-to-moderate bleeding tendency of unknown cause
J Gebhart, C Laczkovics, F Posch, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 15, 2013
Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations
É Katona, L Muszbek, K Devreese, et al.
Lupus
|
August 6, 2010
Clinical and immunoserological characteristics of the transition from primary to overlap antiphospholipid syndrome
K Veres, P Szodoray, Z Szekanecz, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 11, 2016
Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort
R Gindele, Z Oláh, P Ilonczai, et al.
Page
of 12
Search research articles
Search
Showing results (111-120 of 120) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 120 results.
Haemostasis
|
January 1, 1989
Congenital factor XIII deficiency with multiple benign breast tumours and successful pregnancy with substitutive therapy. A case report
Z Boda, G Pfliegler, L Muszbek, et al.
Clinical Chemistry
|
August 14, 1998
A microassay to assess the oxidative resistance of low-density lipoproteins
L Ujhelyi, J Balla, L Muszbek, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 28, 2017
Severe bleeding diatheses in an elderly patient with combined type autoantibody against factor XIII A subunit; novel approach to the diagnosis and classification of anti-factor XIII antibodies
M Kun, N Szuber, É Katona, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 29, 2007
A collaborative study to establish the 1st International Standard for factor XIII plasma
S Raut, R E Merton, P Rigsby, et al.
Blood
|
September 26, 2000
Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia
I Balogh, G Szôke, L Kárpáti, et al.
Tissue & Cell
|
January 1, 1987
Identification of smooth muscle-derived foam cells in the atherosclerotic plaque of human aorta with monoclonal antibody IIG10
M A Glukhova, O I Ornatsky, M G Frid, et al.
Annals of Hematology
|
May 15, 2015
Plasma clot properties in patients with a mild-to-moderate bleeding tendency of unknown cause
J Gebhart, C Laczkovics, F Posch, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
October 15, 2013
Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations
É Katona, L Muszbek, K Devreese, et al.
Lupus
|
August 6, 2010
Clinical and immunoserological characteristics of the transition from primary to overlap antiphospholipid syndrome
K Veres, P Szodoray, Z Szekanecz, et al.
Journal of Thrombosis and Haemostasis : JTH
|
January 11, 2016
Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort
R Gindele, Z Oláh, P Ilonczai, et al.
Page
of 12