Search details
1.
New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia.
Br J Haematol
; 184(5): 855-858, 2019 03.
Article
in English
| MEDLINE | ID: mdl-29527674
2.
Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations.
Br J Haematol
; 186(4): e100-e103, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31016714
3.
Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA-DRB1*11 and DQB1*03 antigens.
Br J Haematol
; 183(2): 317-319, 2018 10.
Article
in English
| MEDLINE | ID: mdl-29076136
4.
Presence of anti-ADAMTS13 antibodies in obesity.
Eur J Clin Invest
; 42(11): 1197-204, 2012 Nov.
Article
in English
| MEDLINE | ID: mdl-22957496
5.
Thrombopoietin receptor agonists as second-line therapy in splenectomy-eligible persistent immune thrombocytopenia: a case series.
Blood Coagul Fibrinolysis
; 30(6): 295-299, 2019 Sep.
Article
in English
| MEDLINE | ID: mdl-31259778
6.
Activated Platelet-Derived and Leukocyte-Derived Circulating Microparticles and the Risk of Thrombosis in Heparin-Induced Thrombocytopenia: A Role for PF4-Bearing Microparticles?
Cytometry B Clin Cytom
; 94(2): 334-341, 2018 03.
Article
in English
| MEDLINE | ID: mdl-28052584
7.
A family with factor-XI deficiency due to a compound heterozygosis between Gln 47 Pro (new mutation) in exon 3 and Leu 619 Pro in exon 15.
Blood Coagul Fibrinolysis
; 25(2): 191-5, 2014 Mar.
Article
in English
| MEDLINE | ID: mdl-24121361
8.
Occurrence of thrombosis in congenital thrombocytopenic disorders: a critical annotation of the literature.
Blood Coagul Fibrinolysis
; 24(1): 18-22, 2013 Jan.
Article
in English
| MEDLINE | ID: mdl-23037321
Results
1 -
8
de 8
1
Next >
>>