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Artur Oliver

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Articles 10
Citations 105
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Recent Articles
1.
Llobet D, Vallve C, Tirado I, Vilalta N, Carrasco M, Oliver A, et al.
Blood Coagul Fibrinolysis . 2020 Dec; 32(2):122-131. PMID: 33337623
The aim of the study was to determine whether platelet hyperaggregability correlates with short closure times (PFA-100) and if hyperaggregability is associated with the risk of venous thrombosis in a...
2.
Llobet D, Vallve C, Tirado I, Vilalta N, Murillo J, Cuevas B, et al.
Thromb Res . 2019 Aug; 181:99-105. PMID: 31382081
Introduction: Platelet hyper-reactivity has been associated with thrombosis and high levels of human vesicle-associated membrane protein 8 (VAMP8) and serotonin transporter (SERT). Two polymorphisms (rs1010 of VAMP8 gene and in...
3.
Olivera P, Gabilondo M, Constans M, Tassies D, Plensa E, Pons V, et al.
Med Clin (Barc) . 2018 Apr; 151(5):210.e1-210.e13. PMID: 29602444
Background And Objectives: In recent years, direct oral anticoagulants (DOACs) have become an alternative to vitamin K antagonists (VKA) for the prevention of stroke and systemic embolism in patients with...
4.
Bullich G, Ballarin J, Oliver A, Ayasreh N, Silva I, Santin S, et al.
Clin J Am Soc Nephrol . 2013 Nov; 9(2):335-43. PMID: 24262501
Background And Objectives: Single nucleotide polymorphisms (SNPs) within HLA complex class II HLA-DQ α-chain 1 (HLA-DQA1) and M-type phospholipase A2 receptor (PLA2R1) genes were identified as strong risk factors for...
5.
Krall P, Pineda C, Ruiz P, Ejarque L, Vendrell T, Camacho J, et al.
Pediatr Nephrol . 2013 Oct; 29(2):223-34. PMID: 24162162
Background: Genetic diagnosis of autosomal recessive polycystic kidney disease (ARPKD) is challenging due to the length and allelic heterogeneity of the PKHD1 gene. Mutations appear to be clustered at specific...
6.
Borrell M, Tirado I, Mateo J, Oliver A, Santamaria A, Fontcuberta J
Haematologica . 2008 May; 93(7):1115-7. PMID: 18508792
No abstract available.
7.
Marin-Aguilera M, Mengual L, Burset M, Oliver A, Ars E, Ribal M, et al.
Eur Urol . 2008 May; 54(6):1363-72. PMID: 18486306
Background: Routine histologic analysis of lymph nodes (LN) for detecting disseminated bladder urothelial carcinoma (BUC) lacks sensitivity. Objective: To identify and test potential mRNA markers of BUC dissemination in LN...
8.
Mengual L, Marin-Aguilera M, Ribal M, Burset M, Villavicencio H, Oliver A, et al.
Eur Urol . 2007 Mar; 52(3):752-9. PMID: 17379395
Objective: To evaluate the use of a multiprobe fluorescent in situ hybridization (FISH) assay for determining the response of patients with high-risk superficial bladder tumour (HRSBT) to bacillus Calmette-Guérin (BCG)...
9.
Marin-Aguilera M, Mengual L, Ribal M, Burset M, Arce Y, Ars E, et al.
Cancer Genet Cytogenet . 2007 Feb; 173(2):131-5. PMID: 17321328
We evaluated the performance of a multiprobe FISH (fluorescence in situ hybridization) assay for noninvasive detection of superficial urothelial carcinoma (UC) in the bladder, in comparison to urinary cytology. Voided...
10.
Tirado I, Soria J, Mateo J, Oliver A, Souto J, Santamaria A, et al.
Thromb Haemost . 2004 Apr; 91(5):899-904. PMID: 15116249
In a family-based study called GAIT (Genetic Analysis of Idiopathic Thrombophilia) that included a genome-wide scan we demonstrated that a polymorphism (46C-->T) in the F12 locus jointly influences variability of...