Detalhe da pesquisa
1.
[Congenital thrombotic thrombocytopenic purpura diagnosed in adulthood after repeated thrombocytopenia since neonatal period].
Rinsho Ketsueki;
65(3): 142-146, 2024.
Artigo
em Japonês
| MEDLINE | ID: mdl-38569856
2.
von Willebrand factor Ristocetin co-factor activity to von Willebrand factor antigen level ratio for diagnosis of acquired von Willebrand syndrome caused by aortic stenosis.
Res Pract Thromb Haemost;
8(1): 102284, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38268521
3.
Diagnostic and treatment guidelines for thrombotic thrombocytopenic purpura (TTP) in Japan 2023.
Int J Hematol;
118(5): 529-546, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37689812
4.
Three Cases of Unprovoked Venous Thromboembolism with Prothrombin p.Arg596Gln Variant and a Literature Review of Antithrombin Resistance.
Intern Med;
62(6): 885-888, 2023 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35945029
5.
P2Y12 Reaction Units and Clinical Outcomes in Acute Large Artery Atherosclerotic Stroke: A Multicenter Prospective Study.
J Atheroscler Thromb;
30(1): 39-55, 2023 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35249906
6.
Siglec-5 and Siglec-14 mediate the endocytosis of ADAMTS13.
Thromb Res;
219: 49-59, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36116391
7.
Alpha-HIT assay: A new assay for heparin-induced thrombocytopenia antibody detection using FcγRIIa-coated beads and Alpha technology.
Res Pract Thromb Haemost;
6(7): e12818, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37602359
8.
First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.
Haematologica;
107(1): 330-333, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34647440
9.
V-ATPase V0a1 promotes Weibel-Palade body biogenesis through the regulation of membrane fission.
Elife;
102021 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34904569
10.
Commonly used anti-von Willebrand factor antibody for multimer analysis cross-reacts with fibronectin, which is difficult to distinguish from von Willebrand factor.
Res Pract Thromb Haemost;
5(6): e12598, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34568727
11.
A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder.
Blood Adv;
5(19): 3830-3838, 2021 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34474479
12.
Arf GTPase-activating proteins SMAP1 and AGFG2 regulate the size of Weibel-Palade bodies and exocytosis of von Willebrand factor.
Biol Open;
10(9)2021 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34369554
13.
Current prophylactic plasma infusion protocols do not adequately prevent long-term cumulative organ damage in the Japanese congenital thrombotic thrombocytopenic purpura cohort.
Br J Haematol;
194(2): 444-452, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34046888
14.
Carrier frequencies of antithrombin, protein C, and protein S deficiency variants estimated using a public database and expression experiments.
Res Pract Thromb Haemost;
5(1): 179-186, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33537542
15.
Derlin-3 Is Required for Changes in ERAD Complex Formation under ER Stress.
Int J Mol Sci;
21(17)2020 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32858914
16.
Success and limitations of plasma treatment in pregnant women with congenital thrombotic thrombocytopenic purpura.
J Thromb Haemost;
18(11): 2929-2941, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33433066
17.
Cerebral venous sinus thrombosis associated with protein S deficiency during pregnancy: a case report.
J Obstet Gynaecol;
40(1): 135-136, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31475594
18.
Predictive value of protein S-specific activity and ELISA testing in patients with the protein S K196E mutation.
Thromb Res;
185: 1-4, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31731088
19.
Knock-in mice bearing constitutively active αIIb(R990W) mutation develop macrothrombocytopenia with severe platelet dysfunction.
J Thromb Haemost;
18(2): 497-509, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31691484
20.
Novel CFHR2-CFHR1 Hybrid in C3 Glomerulopathy Identified by Genomic Structural Variation Analysis.
Kidney Int Rep;
4(12): 1759-1762, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31844814