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Temporal changes in atmospheric mercury concentrations at a background mountain site downwind of the East Asia continent in 2006-2016.

Nguyen LSP, Sheu GR, Lin DW, Lin NH.

Sci Total Environ. 2019 May 31;686:1049-1056. doi: 10.1016/j.scitotenv.2019.05.425. [Epub ahead of print]


Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disorders.

Fayssoil A, Nguyen LS, Ogna A, Stojkovic T, Meng P, Mompoint D, Carlier R, Prigent H, Clair B, Behin A, Laforet P, Bassez G, Crenn P, Orlikowski D, Annane D, Eymard B, Lofaso F.

PLoS One. 2019 Apr 24;14(4):e0214288. doi: 10.1371/journal.pone.0214288. eCollection 2019.


Sirolimus and mTOR Inhibitors: A Review of Side Effects and Specific Management in Solid Organ Transplantation.

Nguyen LS, Vautier M, Allenbach Y, Zahr N, Benveniste O, Funck-Brentano C, Salem JE.

Drug Saf. 2019 Mar 13. doi: 10.1007/s40264-019-00810-9. [Epub ahead of print] Review.


Cardiac arrhythmia considerations of hormone cancer therapies.

Barber M, Nguyen LS, Wassermann J, Spano JP, Funck-Brentano C, Salem JE.

Cardiovasc Res. 2019 Apr 15;115(5):878-894. doi: 10.1093/cvr/cvz020.


Accuracy of B-natriuretic peptide for the diagnosis of decompensated heart failure in muscular dystrophies patients with chronic respiratory failure.

Meng P, Nguyen LS, Jabbour F, Ogna A, Clair B, Orlikowski D, Annane D, Lofaso F, Fayssoil A.

Neurol Int. 2018 Dec 20;10(4):7917. doi: 10.4081/ni.2018.7917. eCollection 2018 Dec 5.


Relation between baseline LDL-cholesterol and cardiovascular outcomes in high cardiovascular risk hypertensive patients: A post-hoc SPRINT data analysis.

Nguyen LS, Procopi N, Salem JE, Squara P, Funck-Brentano C.

Int J Cardiol. 2019 Jul 1;286:159-161. doi: 10.1016/j.ijcard.2019.01.048. Epub 2019 Jan 15.


Respiratory Variability of Pulmonary Velocity-Time Integral As a New Gauge of Fluid Responsiveness For Mechanically Ventilated Patients in the ICU.

Gavaud A, Nguyen LS, Caubel A, Grillet G, Donal E, Belliard G.

Crit Care Med. 2019 Apr;47(4):e310-e316. doi: 10.1097/CCM.0000000000003642.


Evaluation of neutrophil gelatinase-associated lipocalin and cystatin C as biomarkers of acute kidney injury after ST-segment elevation myocardial infarction treated by percutaneous coronary intervention.

Nguyen LS, Spagnoli V, Kerneis M, Hauguel-Moreau M, Barthélémy O, Collet JP, Montalescot G, Silvain J.

Arch Cardiovasc Dis. 2019 Mar;112(3):180-186. doi: 10.1016/j.acvd.2018.11.006. Epub 2019 Jan 9.


Percutaneous versus surgical femoro-femoral veno-arterial ECMO: a propensity score matched study.

Danial P, Hajage D, Nguyen LS, Mastroianni C, Demondion P, Schmidt M, Bouglé A, Amour J, Leprince P, Combes A, Lebreton G.

Intensive Care Med. 2018 Dec;44(12):2153-2161. doi: 10.1007/s00134-018-5442-z. Epub 2018 Nov 14.


High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect.

Medina-Cano D, Ucuncu E, Nguyen LS, Nicouleau M, Lipecka J, Bizot JC, Thiel C, Foulquier F, Lefort N, Faivre-Sarrailh C, Colleaux L, Guerrera IC, Cantagrel V.

Elife. 2018 Oct 12;7. pii: e38309. doi: 10.7554/eLife.38309.


Effect of recipient gender and donor-specific antibodies on antibody-mediated rejection after heart transplantation.

Nguyen LS, Coutance G, Salem JE, Ouldamar S, Lebreton G, Combes A, Amour J, Laali M, Leprince P, Varnous S.

Am J Transplant. 2019 Apr;19(4):1160-1167. doi: 10.1111/ajt.15133. Epub 2018 Oct 29.


Copeptin as a prognostic biomarker in acute myocardial infarction.

Lattuca B, Sy V, Nguyen LS, Bernard M, Zeitouni M, Overtchouk P, Yan Y, Hammoudi N, Ceccaldi A, Collet JP, Kerneis M, Diallo A, Montalescot G, Silvain J.

Int J Cardiol. 2019 Jan 1;274:337-341. doi: 10.1016/j.ijcard.2018.09.022. Epub 2018 Sep 6.


Distal duplication of chromosome 16q22.1q23.1 in a Vietnamese patient with midface hypoplasia and intellectual disability.

Nguyen HH, Pham VA, Barcia G, Malan V, Nguyen KLT, Ngo DN, Nguyen TH, Landrieu P, Colleaux L, Nong VH, Nguyen LS.

Am J Med Genet A. 2018 Sep;176(9):1981-1984. doi: 10.1002/ajmg.a.40375. Epub 2018 Sep 4.


Intravenous ivabradine versus placebo in patients with low cardiac output syndrome treated by dobutamine after elective coronary artery bypass surgery: a phase 2 exploratory randomized controlled trial.

Nguyen LS, Squara P, Amour J, Carbognani D, Bouabdallah K, Thierry S, Apert-Verneuil C, Moyne A, Cholley B.

Crit Care. 2018 Aug 17;22(1):193. doi: 10.1186/s13054-018-2124-8.


Nonselective Chemical Inhibition of Sec7 Domain-Containing ARF GTPase Exchange Factors.

Mishev K, Lu Q, Denoo B, Peurois F, Dejonghe W, Hullaert J, De Rycke R, Boeren S, Bretou M, De Munck S, Sharma I, Goodman K, Kalinowska K, Storme V, Nguyen LSL, Drozdzecki A, Martins S, Nerinckx W, Audenaert D, Vert G, Madder A, Otegui MS, Isono E, Savvides SN, Annaert W, De Vries S, Cherfils J, Winne J, Russinova E.

Plant Cell. 2018 Oct;30(10):2573-2593. doi: 10.1105/tpc.18.00145. Epub 2018 Jul 17.


Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders.

Nguyen LS, Fregeac J, Bole-Feysot C, Cagnard N, Iyer A, Anink J, Aronica E, Alibeu O, Nitschke P, Colleaux L.

Mol Autism. 2018 Jun 19;9:38. doi: 10.1186/s13229-018-0219-3. eCollection 2018.


Effects of Home Mechanical Ventilation on Left Ventricular Function in Sarcoglycanopathies (Limb Girdle Muscular Dystrophies).

Fayssoil A, Nguyen LS, Ogna A, Meng P, Nardi O, Laforet P, Clair B, Prigent H, Lofaso F, Leturcq F, Yaou RB, Annane D, Orlikowski D.

Am J Cardiol. 2018 Jul 15;122(2):353-355. doi: 10.1016/j.amjcard.2018.04.001. Epub 2018 Apr 16.


Effect of additional antihypertensive medications in patients with high-risk hypertension: a post hoc analysis of the SPRINT (Systolic Blood Pressure Intervention Trial) database.

Nguyen LS.

J Clin Hypertens (Greenwich). 2018 Apr;20(4):814-815. doi: 10.1111/jch.13258. Epub 2018 Mar 15. No abstract available.


Heart failure with preserved ejection fraction as an independent risk factor of mortality after cardiothoracic surgery.

Nguyen LS, Baudinaud P, Brusset A, Nicot F, Pechmajou L, Salem JE, Estagnasie P, Squara P.

J Thorac Cardiovasc Surg. 2018 Jul;156(1):188-193.e2. doi: 10.1016/j.jtcvs.2018.02.011. Epub 2018 Feb 13.


Whole-exome sequence analysis highlights the role of unmasked recessive mutations in copy number variants with incomplete penetrance.

Egloff M, Nguyen LS, Siquier-Pernet K, Cormier-Daire V, Baujat G, Attié-Bitach T, Bole-Feysot C, Nitschke P, Vekemans M, Colleaux L, Malan V.

Eur J Hum Genet. 2018 Jun;26(6):912-918. doi: 10.1038/s41431-018-0124-4. Epub 2018 Feb 26.


Intravenous amiodarone-induced acute liver failure in cardiac surgery intensive care unit.

Nicot F, Procopi N, Nguyen LS.

Therapie. 2018 Sep;73(4):355-357. doi: 10.1016/j.therap.2017.12.007. Epub 2017 Dec 30. No abstract available.


Performance of existing risk scores around heart transplantation: validation study in a 4-year cohort.

Nguyen LS, Coutance G, Ouldamar S, Zahr N, Brechot N, Galeone A, Bougle A, Lebreton G, Leprince P, Varnous S.

Transpl Int. 2018 May;31(5):520-530. doi: 10.1111/tri.13122. Epub 2018 Feb 21.


Sickle-cell and alpha-thalassemia traits resulting in non-atherosclerotic myocardial infarction: Beyond coincidence?

Nguyen LS, Redheuil A, Mangin O, Salem JE.

World J Clin Cases. 2017 Dec 16;5(12):428-431. doi: 10.12998/wjcc.v5.i12.428.


Complex Association of Sex Hormones on Left Ventricular Systolic Function: Insight into Sexual Dimorphism.

Salem JE, Nguyen LS, Hammoudi N, Preud'homme G, Hulot JS, Leban M, Funck-Brentano C, Touraine P, Isnard R, Bachelot A; CARDIOHCS Study Group.

J Am Soc Echocardiogr. 2018 Feb;31(2):231-240.e1. doi: 10.1016/j.echo.2017.10.017. Epub 2017 Dec 13.


Non-Invasive Monitoring of Cardiac Output in Critical Care Medicine.

Nguyen LS, Squara P.

Front Med (Lausanne). 2017 Nov 20;4:200. doi: 10.3389/fmed.2017.00200. eCollection 2017. Review.


Low tidal volume mechanical ventilation against no ventilation during cardiopulmonary bypass heart surgery (MECANO): study protocol for a randomized controlled trial.

Nguyen LS, Merzoug M, Estagnasie P, Brusset A, Law Koune JD, Aubert S, Waldmann T, Grinda JM, Gibert H, Squara P.

Trials. 2017 Dec 2;18(1):582. doi: 10.1186/s13063-017-2321-9.


Contrast-induced acute kidney injury and mortality in ST elevation myocardial infarction treated with primary percutaneous coronary intervention.

Silvain J, Nguyen LS, Spagnoli V, Kerneis M, Guedeney P, Vignolles N, Cosker K, Barthelemy O, Le Feuvre C, Helft G, Collet JP, Montalescot G.

Heart. 2018 May;104(9):767-772. doi: 10.1136/heartjnl-2017-311975. Epub 2017 Nov 1.


Frequency of Recovery from Complete Atrioventricular Block After Cardiac Surgery.

Socie P, Nicot F, Baudinaud P, Estagnasie P, Brusset A, Squara P, Nguyen LS.

Am J Cardiol. 2017 Nov 15;120(10):1841-1846. doi: 10.1016/j.amjcard.2017.07.090. Epub 2017 Aug 8.


The emerging roles of MicroRNAs in autism spectrum disorders.

Fregeac J, Colleaux L, Nguyen LS.

Neurosci Biobehav Rev. 2016 Dec;71:729-738. doi: 10.1016/j.neubiorev.2016.10.018. Epub 2016 Oct 25. Review.


Sensitivity of a tropical micro-crustacean (Daphnia lumholtzi) to trace metals tested in natural water of the Mekong River.

Dao TS, Le VN, Bui BT, Dinh KV, Wiegand C, Nguyen TS, Dao CT, Nguyen VD, To TH, Nguyen LS, Vo TG, Vo TM.

Sci Total Environ. 2017 Jan 1;574:1360-1370. doi: 10.1016/j.scitotenv.2016.08.049. Epub 2016 Aug 12.


Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology.

Nguyen LS, Lepleux M, Makhlouf M, Martin C, Fregeac J, Siquier-Pernet K, Philippe A, Feron F, Gepner B, Rougeulle C, Humeau Y, Colleaux L.

Mol Autism. 2016 Jan 8;7:1. doi: 10.1186/s13229-015-0064-6. eCollection 2016.


A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy.

Nguyen LS, Schneider T, Rio M, Moutton S, Siquier-Pernet K, Verny F, Boddaert N, Desguerre I, Munich A, Rosa JL, Cormier-Daire V, Colleaux L.

Eur J Hum Genet. 2016 Mar;24(3):455-8. doi: 10.1038/ejhg.2015.140. Epub 2015 Jul 8.


Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.

Tan C, Shard C, Ranieri E, Hynes K, Pham DH, Leach D, Buchanan G, Corbett M, Shoubridge C, Kumar R, Douglas E, Nguyen LS, Mcmahon J, Sadleir L, Specchio N, Marini C, Guerrini R, Moller RS, Depienne C, Haan E, Thomas PQ, Berkovic SF, Scheffer IE, Gecz J.

Hum Mol Genet. 2015 Sep 15;24(18):5250-9. doi: 10.1093/hmg/ddv245. Epub 2015 Jun 29.


HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.

Jolly LA, Nguyen LS, Domingo D, Sun Y, Barry S, Hancarova M, Plevova P, Vlckova M, Havlovicova M, Kalscheuer VM, Graziano C, Pippucci T, Bonora E, Sedlacek Z, Gecz J.

Hum Mol Genet. 2015 Jun 15;24(12):3335-47. doi: 10.1093/hmg/ddv083. Epub 2015 Mar 3.


Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.

McMichael G, Bainbridge MN, Haan E, Corbett M, Gardner A, Thompson S, van Bon BW, van Eyk CL, Broadbent J, Reynolds C, O'Callaghan ME, Nguyen LS, Adelson DL, Russo R, Jhangiani S, Doddapaneni H, Muzny DM, Gibbs RA, Gecz J, MacLennan AH.

Mol Psychiatry. 2015 Feb;20(2):176-82. doi: 10.1038/mp.2014.189. Epub 2015 Feb 10.


Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.

Homan CC, Kumar R, Nguyen LS, Haan E, Raymond FL, Abidi F, Raynaud M, Schwartz CE, Wood SA, Gecz J, Jolly LA.

Am J Hum Genet. 2014 Mar 6;94(3):470-8. doi: 10.1016/j.ajhg.2014.02.004.


Nonsense-mediated mRNA decay: inter-individual variability and human disease.

Nguyen LS, Wilkinson MF, Gecz J.

Neurosci Biobehav Rev. 2014 Oct;46 Pt 2:175-86. doi: 10.1016/j.neubiorev.2013.10.016. Epub 2013 Nov 14. Review.


Rare copy number variation in cerebral palsy.

McMichael G, Girirajan S, Moreno-De-Luca A, Gecz J, Shard C, Nguyen LS, Nicholl J, Gibson C, Haan E, Eichler E, Martin CL, MacLennan A.

Eur J Hum Genet. 2014 Jan;22(1):40-5. doi: 10.1038/ejhg.2013.93. Epub 2013 May 22.


ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.

Hirata H, Nanda I, van Riesen A, McMichael G, Hu H, Hambrock M, Papon MA, Fischer U, Marouillat S, Ding C, Alirol S, Bienek M, Preisler-Adams S, Grimme A, Seelow D, Webster R, Haan E, MacLennan A, Stenzel W, Yap TY, Gardner A, Nguyen LS, Shaw M, Lebrun N, Haas SA, Kress W, Haaf T, Schellenberger E, Chelly J, Viot G, Shaffer LG, Rosenfeld JA, Kramer N, Falk R, El-Khechen D, Escobar LF, Hennekam R, Wieacker P, Hübner C, Ropers HH, Gecz J, Schuelke M, Laumonnier F, Kalscheuer VM.

Am J Hum Genet. 2013 May 2;92(5):681-95. doi: 10.1016/j.ajhg.2013.03.021. Epub 2013 Apr 25.


Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disability.

Melko M, Nguyen LS, Shaw M, Jolly L, Bardoni B, Gecz J.

Hum Mol Genet. 2013 Aug 1;22(15):2984-91. doi: 10.1093/hmg/ddt155. Epub 2013 Apr 5.


Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.

Nguyen LS, Kim HG, Rosenfeld JA, Shen Y, Gusella JF, Lacassie Y, Layman LC, Shaffer LG, Gécz J.

Hum Mol Genet. 2013 May 1;22(9):1816-25. doi: 10.1093/hmg/ddt035. Epub 2013 Jan 31.


Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay.

Lynch SA, Nguyen LS, Ng LY, Waldron M, McDonald D, Gecz J.

Eur J Med Genet. 2012 Aug-Sep;55(8-9):476-9. doi: 10.1016/j.ejmg.2012.03.010. Epub 2012 Apr 25.


Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.

Nguyen LS, Jolly L, Shoubridge C, Chan WK, Huang L, Laumonnier F, Raynaud M, Hackett A, Field M, Rodriguez J, Srivastava AK, Lee Y, Long R, Addington AM, Rapoport JL, Suren S, Hahn CN, Gamble J, Wilkinson MF, Corbett MA, Gecz J.

Mol Psychiatry. 2012 Nov;17(11):1103-15. doi: 10.1038/mp.2011.163. Epub 2011 Dec 20.


CCDC22: a novel candidate gene for syndromic X-linked intellectual disability.

Voineagu I, Huang L, Winden K, Lazaro M, Haan E, Nelson J, McGaughran J, Nguyen LS, Friend K, Hackett A, Field M, Gecz J, Geschwind D.

Mol Psychiatry. 2012 Jan;17(1):4-7. doi: 10.1038/mp.2011.95. Epub 2011 Aug 9. No abstract available.


Occupational fatalities, injuries, illnesses, and related economic loss in the wholesale and retail trade sector.

Anderson VP, Schulte PA, Sestito J, Linn H, Nguyen LS.

Am J Ind Med. 2010 Jul;53(7):673-85. doi: 10.1002/ajim.20813. Review.


Vision-based system for the control and measurement of wastewater flow rate in sewer systems.

Nguyen LS, Schaeli B, Sage D, Kayal S, Jeanbourquin D, Barry DA, Rossi L.

Water Sci Technol. 2009;60(9):2281-9. doi: 10.2166/wst.2009.659.


A UPF3-mediated regulatory switch that maintains RNA surveillance.

Chan WK, Bhalla AD, Le Hir H, Nguyen LS, Huang L, Gécz J, Wilkinson MF.

Nat Struct Mol Biol. 2009 Jul;16(7):747-53. doi: 10.1038/nsmb.1612. Epub 2009 Jun 7.


Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism.

Laumonnier F, Shoubridge C, Antar C, Nguyen LS, Van Esch H, Kleefstra T, Briault S, Fryns JP, Hamel B, Chelly J, Ropers HH, Ronce N, Blesson S, Moraine C, Gécz J, Raynaud M.

Mol Psychiatry. 2010 Jul;15(7):767-76. doi: 10.1038/mp.2009.14. Epub 2009 Feb 24.


A randomized trial of the effect of automated ventricular capture on device longevity and threshold measurement in pacemaker patients.

Koplan BA, Gilligan DM, Nguyen LS, Lau TK, Thackeray LM, Berg KC; ULTRA Study Investigators.

Pacing Clin Electrophysiol. 2008 Nov;31(11):1467-74. doi: 10.1111/j.1540-8159.2008.01211.x.


Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.

Tarpey PS, Raymond FL, Nguyen LS, Rodriguez J, Hackett A, Vandeleur L, Smith R, Shoubridge C, Edkins S, Stevens C, O'Meara S, Tofts C, Barthorpe S, Buck G, Cole J, Halliday K, Hills K, Jones D, Mironenko T, Perry J, Varian J, West S, Widaa S, Teague J, Dicks E, Butler A, Menzies A, Richardson D, Jenkinson A, Shepherd R, Raine K, Moon J, Luo Y, Parnau J, Bhat SS, Gardner A, Corbett M, Brooks D, Thomas P, Parkinson-Lawrence E, Porteous ME, Warner JP, Sanderson T, Pearson P, Simensen RJ, Skinner C, Hoganson G, Superneau D, Wooster R, Bobrow M, Turner G, Stevenson RE, Schwartz CE, Futreal PA, Srivastava AK, Stratton MR, Gécz J.

Nat Genet. 2007 Sep;39(9):1127-33. Epub 2007 Aug 19.

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