A Veyradier
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Explore the profile of A Veyradier including associated specialties, affiliations and a list of published articles.
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Articles
48
Citations
570
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Recent Articles
1.
Prevel R, Roubaud-Baudron C, Tellier E, Le Besnerais M, Kaplanski G, Veyradier A, et al.
Rev Med Interne
. 2021 Jan;
42(3):202-209.
PMID: 33455838
Immune Thrombotic Thrombocytopenic Purpura (iTTP) is a rare but severe disease with a mortality rate of almost 100 % in the absence of adequate treatment. iTTP is caused by a...
2.
Benhamou Y, Sauvetre G, Grange S, Veyradier A, Coppo P
Rev Med Interne
. 2020 Jul;
41(12):809-813.
PMID: 32727695
Introduction: Thrombotic thrombocytopenic purpura (TTP) is a devastating disease characterized by disseminated microvascular thrombosis. Despite pro-thrombotic predisposing conditions, the prevalence of macrovascular venous thrombosis event (VTE) in immune-mediated TTP (iTTP)...
3.
Poullin P, Bornet C, Veyradier A, Coppo P
Drugs Today (Barc)
. 2019 Jun;
55(6):367-376.
PMID: 31250841
Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a rare and life-threatening disease characterized by microangiopathic hemolytic anemia, thrombocytopenia and multiorgan failure, resulting from autoantibody-mediated severe A disintegrin and metalloproteinase with thrombospondin...
4.
Roose E, Schelpe A, Joly B, Peetermans M, Verhamme P, Voorberg J, et al.
J Thromb Haemost
. 2017 Dec;
16(2):378-388.
PMID: 29222940
Summary: Background Acquired thrombotic thrombocytopenic purpura (aTTP) is an autoimmune disorder characterized by absent ADAMTS-13 activity and the presence of anti-ADAMTS-13 autoantibodies. Recently, it was shown that ADAMTS-13 adopts a...
5.
Tersteeg C, Joly B, Gils A, Lijnen R, Deckmyn H, Declerck P, et al.
J Thromb Haemost
. 2017 Oct;
15(12):2432-2442.
PMID: 28981198
Summary: Background Thrombotic thrombocytopenic purpura (TTP) is an acute life-threatening pathology, caused by occlusive von Willebrand factor (VWF)-rich microthrombi that accumulate in the absence of ADAMTS-13. We previously demonstrated that...
6.
Le Besnerais M, Favre J, Denis C, Mulder P, Martinet J, Nicol L, et al.
J Thromb Haemost
. 2016 Aug;
14(10):1917-1930.
PMID: 27501520
Summary: Background Cardiac alterations represent a major cause of mortality in patients with thrombotic thrombocytopenic purpura (TTP). Endothelial injury remains poorly defined, but seems to be a key initiating event...
7.
Coppo P, Corre E, Rondeau E, Benhamou Y, Bachet A, Stepanian A, et al.
Rev Med Interne
. 2015 Dec;
37(8):514-20.
PMID: 26681105
Thrombotic microangiopathies (TMA) represent rare diseases requiring a high skill for their management that deserved in France the identification of a dedicated National reference center. TMA are short-term life-threatening diseases;...
8.
Pepin M, KleinJan A, Hajage D, Buller H, Di Nisio M, Kamphuisen P, et al.
J Thromb Haemost
. 2015 Nov;
14(2):306-15.
PMID: 26589836
Unlabelled: ESSENTIALS: Cancer patients are at high risk of venous thromboembolism (VTE). In this study, cases and controls were cancer patients who did or did not develop VTE. von Willebrand...
9.
Ghariani I, Jmili-Braham N, Azzebi O, Kortas M, Veyradier A, Bakir L
Arch Pediatr
. 2015 Nov;
23(1):78-81.
PMID: 26552625
We report the case of a newborn presenting with hemolytic anemia, thrombocytopenia, hyperbilirubinemia, and renal failure in the first hours of life. An early plasmatherapy was undertaken, with good outcome....
10.
Joly B, dOiron R, Desconclois C, Bendelac L, Rafowicz A, Meyzer C, et al.
Arch Pediatr
. 2015 Sep;
22(11):1167-70.
PMID: 26412326
Henoch-Schönlein purpura is a common form of immunological vasculitis in children. Hemophilia A is a genetic disorder, inherited in a X-linked recessive pattern, and characterized by spontaneous hemorrhage or prolonged...