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Items: 1 to 50 of 198

1.

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation.

Santori M, Gil R, Blanco-Verea A, Riuró H, Díaz-Castro Ó, López-Abel B, Brugada R, Carracedo Á, Pérez GJ, Scornik FS, Brion M.

Forensic Sci Int Genet. 2019 Nov;43:102159. doi: 10.1016/j.fsigen.2019.102159. Epub 2019 Aug 31.

PMID:
31522018
2.

Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths.

Martinez-Matilla M, Blanco-Verea A, Santori M, Ansede-Bermejo J, Ramos-Luis E, Gil R, Bermejo AM, Lotufo-Neto F, Hirata MH, Brisighelli F, Paramo M, Carracedo A, Brion M.

Forensic Sci Int Genet. 2019 Sep;42:203-212. doi: 10.1016/j.fsigen.2019.07.010. Epub 2019 Jul 18.

PMID:
31376648
3.

A Patient-Tailored Evidence-Based Approach for Developing Early Neuropsychological Training Programs in Addiction Settings.

Rolland B, D'Hondt F, Montègue S, Brion M, Peyron E, D'Aviau de Ternay J, de Timary P, Nourredine M, Maurage P.

Neuropsychol Rev. 2019 Mar;29(1):103-115. doi: 10.1007/s11065-018-9395-3. Epub 2019 Jan 3. Review.

PMID:
30607658
4.

Innovative Strategies in Heart Failure: Present and Future.

Rodríguez-Mañero M, Grigorian-Shamagian L, Rábago G, Abou-Jokh C, Álvarez B, Brion M, González-Juanatey JR.

Arch Med Res. 2018 Nov;49(8):558-567. doi: 10.1016/j.arcmed.2018.12.011. Epub 2018 Dec 31. Review.

PMID:
30606503
5.

Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analyses.

Scheiper S, Ramos-Luis E, Blanco-Verea A, Niess C, Beckmann BM, Schmidt U, Kettner M, Geisen C, Verhoff MA, Brion M, Kauferstein S.

Forensic Sci Int. 2018 Dec;293:70-76. doi: 10.1016/j.forsciint.2018.09.034. Epub 2018 Oct 26.

PMID:
30415094
6.

A dual-process exploration of binge drinking: Evidence through behavioral and electrophysiological findings.

Lannoy S, Dormal V, Billieux J, Brion M, D'Hondt F, Maurage P.

Addict Biol. 2018 Oct 29. doi: 10.1111/adb.12685. [Epub ahead of print]

PMID:
30370964
7.

The Medical Genome Reference Bank: a whole-genome data resource of 4000 healthy elderly individuals. Rationale and cohort design.

Lacaze P, Pinese M, Kaplan W, Stone A, Brion MJ, Woods RL, McNamara M, McNeil JJ, Dinger ME, Thomas DM.

Eur J Hum Genet. 2019 Feb;27(2):308-316. doi: 10.1038/s41431-018-0279-z. Epub 2018 Oct 24.

8.

A Novel Calsequestrin 2 Deletion Causing Catecholaminergic Polymorphic Ventricular Tachycardia and Sudden Cardiac Death.

Blanco-Verea A, Ramos-Luis E, García-Seara J, Carracedo Á, González-Juanatey JR, Brion M.

Rev Esp Cardiol (Engl Ed). 2019 Aug;72(8):681-683. doi: 10.1016/j.rec.2018.07.005. Epub 2018 Aug 20. English, Spanish. No abstract available.

PMID:
30139651
9.

Research update for articles published in EJCI in 2016.

Adlbrecht C, Blanco-Verea A, Bouzas-Mosquera MC, Brion M, Burtscher M, Carbone F, Chang TT, Charmandari E, Chen JW, Correia-Costa L, Dullaart RPF, Eleftheriades M, Fernandez-Fernandez B, Goliasch G, Gremmel T, Groeneveld ME, Henrique A, Huelsmann M, Jung C, Lichtenauer M, Montecucco F, Nicolaides NC, Niessner A, Palmeira C, Pirklbauer M, Sanchez-Niño MD, Sotiriadis A, Sousa T, Sulzgruber P, van Beek AP, Veronese N, Winter MP, Yeung KK, Bouzas-Mosquera A.

Eur J Clin Invest. 2018 Oct;48(10):e13016. doi: 10.1111/eci.13016. Epub 2018 Sep 16. Review. No abstract available.

PMID:
30099749
10.

Electrophysiological correlates of emotional crossmodal processing in binge drinking.

Lannoy S, D'Hondt F, Dormal V, Blanco M, Brion M, Billieux J, Campanella S, Maurage P.

Cogn Affect Behav Neurosci. 2018 Dec;18(6):1076-1088. doi: 10.3758/s13415-018-0623-3.

PMID:
30094563
11.

Impaired affective prosody decoding in severe alcohol use disorder and Korsakoff syndrome.

Brion M, de Timary P, Mertens de Wilmars S, Maurage P.

Psychiatry Res. 2018 Jun;264:404-406. doi: 10.1016/j.psychres.2018.04.001. Epub 2018 Apr 3.

PMID:
29679843
12.

Affective impairments in binge drinking: Investigation through emotional facial expression decoding.

Lannoy S, Dormal V, Brion M, Gaudelus B, Billieux J, Maurage P.

Compr Psychiatry. 2018 May;83:59-63. doi: 10.1016/j.comppsych.2018.03.004. Epub 2018 Mar 16.

PMID:
29587205
13.

Imbalance between cognitive systems in alcohol-dependence and Korsakoff syndrome: An exploration using the Alcohol Flanker Task.

Brion M, Dormal V, Lannoy S, Mertens S, de Timary P, Maurage P.

J Clin Exp Neuropsychol. 2018 Oct;40(8):820-831. doi: 10.1080/13803395.2018.1438371. Epub 2018 Mar 6.

PMID:
29509075
14.

Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy.

Huin V, Strubi-Vuillaume I, Dujardin K, Brion M, Delliaux M, Dellacherie D, Cuvellier JC, Cuisset JM, Riquet A, Moreau C, Defebvre L, Sablonnière B, Devos D.

Parkinsonism Relat Disord. 2017 Dec;45:85-89. doi: 10.1016/j.parkreldis.2017.09.014. Epub 2017 Sep 19.

PMID:
28947073
15.

Crossmodal processing of emotions in alcohol-dependence and Korsakoff syndrome.

Brion M, D'Hondt F, Lannoy S, Pitel AL, Davidoff DA, Maurage P.

Cogn Neuropsychiatry. 2017 Sep;22(5):436-451. doi: 10.1080/13546805.2017.1373639. Epub 2017 Sep 8.

PMID:
28885888
16.

Preserved Crossmodal Integration of Emotional Signals in Binge Drinking.

Lannoy S, Dormal V, Brion M, Billieux J, Maurage P.

Front Psychol. 2017 Jun 15;8:984. doi: 10.3389/fpsyg.2017.00984. eCollection 2017.

17.

Executive functions in alcohol-dependence: A theoretically grounded and integrative exploration.

Brion M, D'Hondt F, Pitel AL, Lecomte B, Ferauge M, de Timary P, Maurage P.

Drug Alcohol Depend. 2017 Aug 1;177:39-47. doi: 10.1016/j.drugalcdep.2017.03.018. Epub 2017 May 19.

PMID:
28554151
18.

Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome.

Franken R, Teixido-Tura G, Brion M, Forteza A, Rodriguez-Palomares J, Gutierrez L, Garcia Dorado D, Pals G, Mulder BJ, Evangelista A.

Heart. 2017 Nov;103(22):1795-1799. doi: 10.1136/heartjnl-2016-310631. Epub 2017 May 3.

PMID:
28468757
19.

Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection.

Gago-Díaz M, Ramos-Luis E, Zoppis S, Zorio E, Molina P, Braza-Boïls A, Giner J, Sobrino B, Amigo J, Blanco-Verea A, Carracedo Á, Brion M.

Int J Legal Med. 2017 Sep;131(5):1211-1219. doi: 10.1007/s00414-017-1583-9. Epub 2017 Apr 8.

PMID:
28391405
20.

Source Memory in Korsakoff Syndrome: Disentangling the Mechanisms of Temporal Confusion.

Brion M, de Timary P, Pitel AL, Maurage P.

Alcohol Clin Exp Res. 2017 Mar;41(3):596-607. doi: 10.1111/acer.13318. Epub 2017 Feb 3.

PMID:
28160301
21.

Calypso: a user-friendly web-server for mining and visualizing microbiome-environment interactions.

Zakrzewski M, Proietti C, Ellis JJ, Hasan S, Brion MJ, Berger B, Krause L.

Bioinformatics. 2017 Mar 1;33(5):782-783. doi: 10.1093/bioinformatics/btw725.

22.

Mining, visualizing and comparing multidimensional biomolecular data using the Genomics Data Miner (GMine) Web-Server.

Proietti C, Zakrzewski M, Watkins TS, Berger B, Hasan S, Ratnatunga CN, Brion MJ, Crompton PD, Miles JJ, Doolan DL, Krause L.

Sci Rep. 2016 Dec 6;6:38178. doi: 10.1038/srep38178.

23.

The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study.

Gago-Díaz M, Brion M, Gallego P, Calvo F, Robledo-Carmona J, Saura D, Sánchez V, Bermejo J, Sevilla T, Newton-Cheh C, Carracedo Á, Muehlschlegel JD, García-Dorado D, Body SC, Evangelista A.

J Mol Cell Cardiol. 2017 Jan;102:3-9. doi: 10.1016/j.yjmcc.2016.11.012. Epub 2016 Nov 25.

PMID:
27894865
24.

ABCC3 Polymorphisms and mRNA Expression Influence the Concentration of a Carboxylic Acid Metabolite in Patients on Clopidogrel and Aspirin Therapy.

Luchessi AD, Concheiro M, Germano JF, Silbiger VN, Bortolin RH, Cruz A, Quintela O, Brion M, Carracedo A, Iñiguez A, Bravo M, López-Rivadulla M, Hirata RD, Sousa AG, Hirata MH.

Basic Clin Pharmacol Toxicol. 2017 May;120(5):466-474. doi: 10.1111/bcpt.12703. Epub 2017 Jan 16.

25.

A functional magnetic resonance imaging investigation of theory of mind impairments in patients with temporal lobe epilepsy.

Hennion S, Delbeuck X, Koelkebeck K, Brion M, Tyvaert L, Plomhause L, Derambure P, Lopes R, Szurhaj W.

Neuropsychologia. 2016 Dec;93(Pt A):271-279. doi: 10.1016/j.neuropsychologia.2016.11.007. Epub 2016 Nov 12.

PMID:
27847305
26.

Medico-legal perspectives on sudden cardiac death in young athletes.

Oliva A, Grassi VM, Campuzano O, Brion M, Arena V, Partemi S, Coll M, Pascali VL, Brugada J, Carracedo A, Brugada R.

Int J Legal Med. 2017 Mar;131(2):393-409. doi: 10.1007/s00414-016-1452-y. Epub 2016 Sep 21. Review.

PMID:
27654714
27.

PRKG1 and genetic diagnosis of early-onset thoracic aortic disease.

Gago-Díaz M, Blanco-Verea A, Teixidó G, Huguet F, Gut M, Laurie S, Gut I, Carracedo Á, Evangelista A, Brion M.

Eur J Clin Invest. 2016 Sep;46(9):787-94. doi: 10.1111/eci.12662. Epub 2016 Aug 18.

PMID:
27442293
28.

Prospective and Retrospective Diagnosis of Barth Syndrome Aided by Next-Generation Sequencing.

Brión M, de Castro López MJ, Santori M, Pérez Muñuzuri A, López Abel B, Baña Souto AM, Martínez Soto MI, Couce ML.

Am J Clin Pathol. 2016 Apr;145(4):507-13. doi: 10.1093/ajcp/aqw025. Epub 2016 Apr 22. Erratum in: Am J Clin Pathol. 2016 Jun;145(6):879.

PMID:
27124939
29.

New Perspectives in the Exploration of Korsakoff's Syndrome: The Usefulness of Neurophysiological Markers.

Brion M, Pitel AL, D'Hondt F.

Front Psychol. 2016 Feb 16;7:168. doi: 10.3389/fpsyg.2016.00168. eCollection 2016.

30.

Chemosensory Dysfunction in Alcohol-Related Disorders: A Joint Exploration of Olfaction and Taste.

Brion M, de Timary P, Vander Stappen C, Guettat L, Lecomte B, Rombaux P, Maurage P.

Chem Senses. 2015 Nov;40(9):605-8. doi: 10.1093/chemse/bjv047. Epub 2015 Sep 9.

PMID:
26354933
31.

Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood.

Santori M, Blanco-Verea A, Gil R, Cortis J, Becker K, Schneider PM, Carracedo A, Brion M.

Arch Dis Child. 2015 Oct;100(10):952-6. doi: 10.1136/archdischild-2015-308200. Epub 2015 Aug 13.

PMID:
26272908
32.

Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young.

Brion M, Sobrino B, Martinez M, Blanco-Verea A, Carracedo A.

Forensic Sci Int Genet. 2015 Sep;18:160-70. doi: 10.1016/j.fsigen.2015.07.010. Epub 2015 Jul 23. Review.

PMID:
26243589
33.

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.

Allegue C, Coll M, Mates J, Campuzano O, Iglesias A, Sobrino B, Brion M, Amigo J, Carracedo A, Brugada P, Brugada J, Brugada R.

PLoS One. 2015 Jul 31;10(7):e0133037. doi: 10.1371/journal.pone.0133037. eCollection 2015.

34.

Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.

Suárez-Rama JJ, Arrojo M, Sobrino B, Amigo J, Brenlla J, Agra S, Paz E, Brión M, Carracedo Á, Páramo M, Costas J.

J Psychiatr Res. 2015 Jul-Aug;66-67:38-44. doi: 10.1016/j.jpsychires.2015.04.013. Epub 2015 Apr 22.

PMID:
25943950
35.

The relationship between surname frequency and Y chromosome variation in Spain.

Martinez-Cadenas C, Blanco-Verea A, Hernando B, Busby GB, Brion M, Carracedo A, Salas A, Capelli C.

Eur J Hum Genet. 2016 Jan;24(1):120-8. doi: 10.1038/ejhg.2015.75. Epub 2015 Apr 22.

36.

Association between SNPs of Metalloproteinases and Prostaglandin F2α Receptor Genes and Latanoprost Response in Open-Angle Glaucoma.

Ussa F, Fernandez I, Brion M, Carracedo A, Blazquez F, Garcia MT, Sanchez-Jara A, De Juan-Marcos L, Jimenez-Carmona S, Juberias JR, Martinez-de-la-Casa JM, Pastor JC.

Ophthalmology. 2015 May;122(5):1040-8.e4. doi: 10.1016/j.ophtha.2014.12.038. Epub 2015 Feb 19.

PMID:
25704319
37.

Behavioural early-life exposures and body composition at age 15 years.

Leary SD, Lawlor DA, Davey Smith G, Brion MJ, Ness AR.

Nutr Diabetes. 2015 Feb 9;5:e150. doi: 10.1038/nutd.2014.47.

38.

Predicting proliferative vitreoretinopathy: temporal and external validation of models based on genetic and clinical variables.

Rojas J, Fernandez I, Pastor JC, MacLaren RE, Ramkissoon Y, Harsum S, Charteris DG, Van Meurs JC, Amarakoon S, Garcia-Arumi J, Ruiz-Moreno JM, Rocha-Sousa A, Brion M, Carracedo A; Genetics on PVR Study Group (web file).

Br J Ophthalmol. 2015 Jan;99(1):41-8. doi: 10.1136/bjophthalmol-2014-305263. Epub 2014 Jul 29.

PMID:
25075124
39.

Revisiting the continuum hypothesis: toward an in-depth exploration of executive functions in korsakoff syndrome.

Brion M, Pitel AL, Beaunieux H, Maurage P.

Front Hum Neurosci. 2014 Jul 4;8:498. doi: 10.3389/fnhum.2014.00498. eCollection 2014. Review.

40.

Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease.

Gago-Díaz M, Blanco-Verea A, Teixidó-Turà G, Valenzuela I, Del Campo M, Borregan M, Sobrino B, Amigo J, García-Dorado D, Evangelista A, Carracedo A, Brion M.

Clin Chim Acta. 2014 Nov 1;437:88-92. doi: 10.1016/j.cca.2014.07.016. Epub 2014 Jul 19.

PMID:
25046559
41.

Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders.

Brion M, Blanco-Verea A, Sobrino B, Santori M, Gil R, Ramos-Luis E, Martinez M, Amigo J, Carracedo A.

Electrophoresis. 2014 Nov;35(21-22):3111-6. doi: 10.1002/elps.201400148. Epub 2014 Aug 6.

PMID:
24981977
42.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

Arking DE, Pulit SL, Crotti L, van der Harst P, Munroe PB, Koopmann TT, Sotoodehnia N, Rossin EJ, Morley M, Wang X, Johnson AD, Lundby A, Gudbjartsson DF, Noseworthy PA, Eijgelsheim M, Bradford Y, Tarasov KV, Dörr M, Müller-Nurasyid M, Lahtinen AM, Nolte IM, Smith AV, Bis JC, Isaacs A, Newhouse SJ, Evans DS, Post WS, Waggott D, Lyytikäinen LP, Hicks AA, Eisele L, Ellinghaus D, Hayward C, Navarro P, Ulivi S, Tanaka T, Tester DJ, Chatel S, Gustafsson S, Kumari M, Morris RW, Naluai ÅT, Padmanabhan S, Kluttig A, Strohmer B, Panayiotou AG, Torres M, Knoflach M, Hubacek JA, Slowikowski K, Raychaudhuri S, Kumar RD, Harris TB, Launer LJ, Shuldiner AR, Alonso A, Bader JS, Ehret G, Huang H, Kao WH, Strait JB, Macfarlane PW, Brown M, Caulfield MJ, Samani NJ, Kronenberg F, Willeit J; CARe Consortium; COGENT Consortium, Smith JG, Greiser KH, Meyer Zu Schwabedissen H, Werdan K, Carella M, Zelante L, Heckbert SR, Psaty BM, Rotter JI, Kolcic I, Polašek O, Wright AF, Griffin M, Daly MJ; DCCT/EDIC, Arnar DO, Hólm H, Thorsteinsdottir U; eMERGE Consortium, Denny JC, Roden DM, Zuvich RL, Emilsson V, Plump AS, Larson MG, O'Donnell CJ, Yin X, Bobbo M, D'Adamo AP, Iorio A, Sinagra G, Carracedo A, Cummings SR, Nalls MA, Jula A, Kontula KK, Marjamaa A, Oikarinen L, Perola M, Porthan K, Erbel R, Hoffmann P, Jöckel KH, Kälsch H, Nöthen MM; HRGEN Consortium, den Hoed M, Loos RJ, Thelle DS, Gieger C, Meitinger T, Perz S, Peters A, Prucha H, Sinner MF, Waldenberger M, de Boer RA, Franke L, van der Vleuten PA, Beckmann BM, Martens E, Bardai A, Hofman N, Wilde AA, Behr ER, Dalageorgou C, Giudicessi JR, Medeiros-Domingo A, Barc J, Kyndt F, Probst V, Ghidoni A, Insolia R, Hamilton RM, Scherer SW, Brandimarto J, Margulies K, Moravec CE, del Greco M F, Fuchsberger C, O'Connell JR, Lee WK, Watt GC, Campbell H, Wild SH, El Mokhtari NE, Frey N, Asselbergs FW, Mateo Leach I, Navis G, van den Berg MP, van Veldhuisen DJ, Kellis M, Krijthe BP, Franco OH, Hofman A, Kors JA, Uitterlinden AG, Witteman JC, Kedenko L, Lamina C, Oostra BA, Abecasis GR, Lakatta EG, Mulas A, Orrú M, Schlessinger D, Uda M, Markus MR, Völker U, Snieder H, Spector TD, Ärnlöv J, Lind L, Sundström J, Syvänen AC, Kivimaki M, Kähönen M, Mononen N, Raitakari OT, Viikari JS, Adamkova V, Kiechl S, Brion M, Nicolaides AN, Paulweber B, Haerting J, Dominiczak AF, Nyberg F, Whincup PH, Hingorani AD, Schott JJ, Bezzina CR, Ingelsson E, Ferrucci L, Gasparini P, Wilson JF, Rudan I, Franke A, Mühleisen TW, Pramstaller PP, Lehtimäki TJ, Paterson AD, Parsa A, Liu Y, van Duijn CM, Siscovick DS, Gudnason V, Jamshidi Y, Salomaa V, Felix SB, Sanna S, Ritchie MD, Stricker BH, Stefansson K, Boyer LA, Cappola TP, Olsen JV, Lage K, Schwartz PJ, Kääb S, Chakravarti A, Ackerman MJ, Pfeufer A, de Bakker PI, Newton-Cheh C.

Nat Genet. 2014 Aug;46(8):826-36. doi: 10.1038/ng.3014. Epub 2014 Jun 22.

43.

Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data.

Chen GB, Lee SH, Brion MJ, Montgomery GW, Wray NR, Radford-Smith GL, Visscher PM; International IBD Genetics Consortium.

Hum Mol Genet. 2014 Sep 1;23(17):4710-20. doi: 10.1093/hmg/ddu174. Epub 2014 Apr 11.

44.

Y-chromosomal DNA analysis in French male lineages.

Ramos-Luis E, Blanco-Verea A, Brión M, Van Huffel V, Sánchez-Diz P, Carracedo A.

Forensic Sci Int Genet. 2014 Mar;9:162-8. doi: 10.1016/j.fsigen.2013.12.008. Epub 2013 Dec 29.

PMID:
24528594
45.

Maternal iron levels early in pregnancy are not associated with offspring IQ score at age 8, findings from a Mendelian randomization study.

Lewis SJ, Bonilla C, Brion MJ, Lawlor DA, Gunnell D, Ben-Shlomo Y, Ness A, Smith GD.

Eur J Clin Nutr. 2014 Apr;68(4):496-502. doi: 10.1038/ejcn.2013.265. Epub 2014 Jan 8.

46.

Mining the human phenome using allelic scores that index biological intermediates.

Evans DM, Brion MJ, Paternoster L, Kemp JP, McMahon G, Munafò M, Whitfield JB, Medland SE, Montgomery GW; GIANT Consortium; CRP Consortium; TAG Consortium, Timpson NJ, St Pourcain B, Lawlor DA, Martin NG, Dehghan A, Hirschhorn J, Smith GD.

PLoS Genet. 2013 Oct;9(10):e1003919. doi: 10.1371/journal.pgen.1003919. Epub 2013 Oct 31.

47.

Calculating statistical power in Mendelian randomization studies.

Brion MJ, Shakhbazov K, Visscher PM.

Int J Epidemiol. 2013 Oct;42(5):1497-501. doi: 10.1093/ije/dyt179.

48.

Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population.

Corton M, Avila-Fernandez A, Vallespín E, López-Molina MI, Almoguera B, Martín-Garrido E, Tatu SD, Khan MI, Blanco-Kelly F, Riveiro-Alvarez R, Brión M, García-Sandoval B, Cremers FPM, Carracedo A, Ayuso C.

Ophthalmology. 2014 Jan;121(1):399-407. doi: 10.1016/j.ophtha.2013.08.028. Epub 2013 Oct 18.

PMID:
24144451
49.

Pharmacogenomics of anti-platelet therapy focused on peripheral blood cells of coronary arterial disease patients.

Luchessi AD, Silbiger VN, Hirata RD, Lima-Neto LG, Cavichioli D, Iñiguez A, Bravo M, Bastos G, Sousa AG, Brión M, Carracedo A, Hirata MH.

Clin Chim Acta. 2013 Oct 21;425:9-17. doi: 10.1016/j.cca.2013.06.021. Epub 2013 Jul 4.

50.

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