Detalhe da pesquisa
1.
Variable Penetrance and Expressivity of a Rare Pore Loss-of-Function Mutation (p.L889V) of Nav1.5 Channels in Three Spanish Families.
Int J Mol Sci
; 25(9)2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38731905
2.
Characterization of a complex CYP2D6 genotype that caused an AmpliChip CYP450 Test no-call in the clinical setting.
Clin Chem Lab Med
; 52(6): 799-807, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24445243
3.
Could Online Education Replace Face-to-Face Education in Diabetes? A Systematic Review.
Diabetes Ther
; 2024 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38743305
4.
Importance of genetic study in elderly patients with transthyretin cardiac amyloidosis. / Relevancia del estudio genético de la amiloidosis cardíaca por transtiretina en el anciano.
Med Clin (Barc)
; 2023 Jul 31.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-37532616
5.
Ten Years of Experience Support Pharmacogenetic Testing to Guide Individualized Drug Therapy.
Pharmaceutics
; 14(1)2022 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35057056
6.
Case Report: Pharmacogenetics Applied to Precision Psychiatry Could Explain the Outcome of a Patient With a New CYP2D6 Genotype.
Front Psychiatry
; 12: 830608, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35281207
7.
Economic Impact of the Application of a Precision Medicine Model (5SPM) on Psychotic Patients.
Pharmgenomics Pers Med
; 14: 1015-1025, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34429634
8.
A rare HCN4 variant with combined sinus bradycardia, left atrial dilatation, and hypertrabeculation/left ventricular noncompaction phenotype.
Rev Esp Cardiol (Engl Ed)
; 74(9): 781-789, 2021 Sep.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-33008772
9.
Usefulness of Pharmacogenetic Analysis in Psychiatric Clinical Practice: A Case Report.
Clin Psychopharmacol Neurosci
; 16(3): 349-357, 2018 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-30121988
10.
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients.
BMC Med Genomics
; 11(1): 58, 2018 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29986705
11.
Pharmacogenetics and the treatment of asthma.
Pharmacogenomics
; 18(13): 1271-1280, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28776467
12.
Assessment and Validation of New Genetic Variants: A Systematic In Silico Approach.
Methods Mol Biol
; 1434: 15-27, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27300528
13.
Role of Pharmacogenetics in Improving the Safety of Psychiatric Care by Predicting the Potential Risks of Mania in CYP2D6 Poor Metabolizers Diagnosed With Bipolar Disorder.
Medicine (Baltimore)
; 95(6): e2473, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26871771
14.
Clinical evaluation of a microsphere bead-based flow cytometry assay for the simultaneous determination of anti-thyroid peroxidase and anti-thyroglobulin antibodies.
Clin Biochem
; 38(11): 966-72, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16168980
15.
Laboratory screening of connective tissue diseases by a new automated ENA screening assay (EliA Symphony) in clinically defined patients.
Clin Chim Acta
; 359(1-2): 109-14, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-15894301
16.
Anti-cyclic citrullinated peptide autoantibodies in IgM rheumatoid factor-positive patients.
Clin Chim Acta
; 354(1-2): 123-30, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15748608
17.
Dose reduction of efavirenz: an observational study describing cost-effectiveness, pharmacokinetics and pharmacogenetics.
Pharmacogenomics
; 15(7): 997-1006, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24956253
18.
Pharmacogenetics to prevent maniac affective switching with treatment for bipolar disorder: CYP2D6.
Pharmacogenomics
; 17(12): 1291-3, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27469479
19.
Primun non nocere, polypharmacy and pharmacogenetics.
Pharmacogenomics
; 16(17): 1903-5, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26554320
20.
Clinical evaluation of cobas core anti-dsDNA EIA quant.
J Clin Lab Anal
; 18(3): 200-5, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15103686