Detalhe da pesquisa
1.
High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.
Haemophilia
; 23(6): e488-e496, 2017 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-28960694
2.
Association of complement receptor 2 polymorphisms with innate resistance to HIV-1 infection.
Genes Immun
; 16(2): 134-41, 2015 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-25569262
3.
Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership.
Br J Dermatol
; 173(5): 1280-3, 2015 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-25996448
4.
Economic Analysis Of Thrombo Incode, A Clinical-Genetic Function For Assessing The Risk Of Venous Thromboembolism.
Value Health
; 17(7): A488, 2014 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-27201446
5.
DNA binding site characterization by means of Rényi entropy measures on nucleotide transitions.
IEEE Trans Nanobioscience
; 7(2): 133-41, 2008 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-18556261
6.
Influence of the substrate's hydrophilicity on the in vitro Schwann cells viability.
J Biomed Mater Res A
; 83(2): 463-70, 2007 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-17477391
7.
Genetic determinants of normal variation in coagulation factor (F) IX levels: genome-wide scan and examination of the FIX structural gene.
J Thromb Haemost
; 4(7): 1537-45, 2006 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-16839351
8.
A locus on chromosome 2 influences levels of tissue factor pathway inhibitor: results from the GAIT study.
Arterioscler Thromb Vasc Biol
; 25(7): 1489-92, 2005 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-15845911
9.
Economic analysis of thrombo inCode, a clinical-genetic function for assessing the risk of venous thromboembolism.
Appl Health Econ Health Policy
; 13(2): 233-42, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25652150
10.
Coagulation factor XII genetic variation, ex vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study.
J Thromb Haemost
; 13(10): 1867-77, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26286125
11.
Different origins and developmental histories of transient neurons in the marginal zone of the fetal and neonatal rat cortex.
J Comp Neurol
; 397(4): 493-518, 1998 Aug 10.
Artigo
Inglês
| MEDLINE | ID: mdl-9699912
12.
Severe type I protein C deficiency in a compound heterozygote for Y124C and Q132X mutations in exon 6 of the PROC gene.
Thromb Haemost
; 74(5): 1215-20, 1995 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-8607097
13.
Severe homozygous protein C deficiency: identification of a splice site missense mutation (184, Q-->H) in exon 7 of the protein C gene.
Thromb Haemost
; 72(1): 65-9, 1994 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-7974377
14.
Ectopic transcript analysis indicates that allelic exclusion is an important cause of type I protein C deficiency in patients with nonsense and frameshift mutations in the PROC gene.
Thromb Haemost
; 75(6): 870-6, 1996 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-8822578
15.
Homozygosity for R87H missense mutation and for a rare intron 7 DNA variant (7054G --> A) in the PROC genes of three siblings initially classified as heterozygotes for protein C deficiency.
Blood Coagul Fibrinolysis
; 7(1): 15-23, 1996 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-8845458
16.
Abnormal polymerization and normal binding of plasminogen and t-PA in three new dysfibrinogenaemias: Barcelona III and IV (gamma Arg 275-->His) and Villajoyosa (gamma Arg 275-->Cys).
Blood Coagul Fibrinolysis
; 6(3): 198-206, 1995 May.
Artigo
Inglês
| MEDLINE | ID: mdl-7654933
17.
Aberrant RNA splicing of the protein C and protein S genes in healthy individuals.
Blood Coagul Fibrinolysis
; 7(6): 625-31, 1996 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-8899152
18.
[Polymorphism MI detected through the enzyme MspI in the study of congenital protein C deficiency]. / Aplicación del polimorfismo MI, reconocido por la enzima MspI, al estudio del déficit congénito de proteína C.
Med Clin (Barc)
; 99(17): 649-52, 1992 Nov 21.
Artigo
Espanhol
| MEDLINE | ID: mdl-1280311
19.
Genetic determinants of plasma ß2-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.
J Thromb Haemost
; 11(3): 521-8, 2013 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-23279374
20.
Neuroprotection of lipoic acid treatment promotes angiogenesis and reduces the glial scar formation after brain injury.
Neuroscience
; 224: 102-15, 2012 Nov 08.
Artigo
Inglês
| MEDLINE | ID: mdl-22917609