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Items: 1 to 50 of 56

1.

NRF2/ARE pathway negatively regulates BACE1 expression and ameliorates cognitive deficits in mouse Alzheimer's models.

Bahn G, Park JS, Yun UJ, Lee YJ, Choi Y, Park JS, Baek SH, Choi BY, Cho YS, Kim HK, Han J, Sul JH, Baik SH, Lim J, Wakabayashi N, Bae SH, Han JW, Arumugam TV, Mattson MP, Jo DG.

Proc Natl Acad Sci U S A. 2019 Jun 18;116(25):12516-12523. doi: 10.1073/pnas.1819541116. Epub 2019 Jun 4.

PMID:
31164420
2.

Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.

Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, Aschauer H, Stamenkovic M, Schlögelhofer M, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, Hinney A, King RA, Fernandez TV, Barta C, Tarnok Z, Nagy P, Depienne C, Worbe Y, Hartmann A, Budman CL, Rizzo R, Lyon GJ, McMahon WM, Batterson JR, Cath DC, Malaty IA, Okun MS, Berlin C, Woods DW, Lee PC, Jankovic J, Robertson MM, Gilbert DL, Brown LW, Coffey BJ, Dietrich A, Hoekstra PJ, Kuperman S, Zinner SH, Luðvigsson P, Sæmundsen E, Thorarensen Ó, Atzmon G, Barzilai N, Wagner M, Moessner R, Ophoff R, Pato CN, Pato MT, Knowles JA, Roffman JL, Smoller JW, Buckner RL, Willsey AJ, Tischfield JA, Heiman GA, Stefansson H, Stefansson K, Posthuma D, Cox NJ, Pauls DL, Freimer NB, Neale BM, Davis LK, Paschou P, Coppola G, Mathews CA, Scharf JM; Tourette Association of America International Consortium for Genetics, the Gilles de la Tourette GWAS Replication Initiative, the Tourette International Collaborative Genetics Study, and the Psychiatric Genomics Consortium Tourette Syndrome Working Group.

Am J Psychiatry. 2019 Mar 1;176(3):217-227. doi: 10.1176/appi.ajp.2018.18070857.

PMID:
30818990
3.

Population structure in genetic studies: Confounding factors and mixed models.

Sul JH, Martin LS, Eskin E.

PLoS Genet. 2018 Dec 27;14(12):e1007309. doi: 10.1371/journal.pgen.1007309. eCollection 2018 Dec. Review.

4.

Understanding the Hidden Complexity of Latin American Population Isolates.

Mooney JA, Huber CD, Service S, Sul JH, Marsden CD, Zhang Z, Sabatti C, Ruiz-Linares A, Bedoya G; Costa Rica/Colombia Consortium for Genetic Investigation of Bipolar Endophenotypes, Freimer N, Lohmueller KE.

Am J Hum Genet. 2018 Nov 1;103(5):707-726. doi: 10.1016/j.ajhg.2018.09.013. Epub 2018 Oct 25.

5.

Laser-Induced Reduction of Graphene Oxide by Intensity-Modulated Line Beam for Supercapacitor Applications.

Tran TX, Choi H, Che CH, Sul JH, Kim IG, Lee SM, Kim JH, In JB.

ACS Appl Mater Interfaces. 2018 Nov 21;10(46):39777-39784. doi: 10.1021/acsami.8b14678. Epub 2018 Nov 12.

PMID:
30371054
6.

Inhibition of Notch1 induces population and suppressive activity of regulatory T cell in inflammatory arthritis.

Choi BY, Choi Y, Park JS, Kang LJ, Baek SH, Park JS, Bahn G, Cho Y, Kim HK, Han J, Sul JH, Baik SH, Hyun DH, Arumugam TV, Yang S, Han JW, Kang YM, Cho YW, Park JH, Jo DG.

Theranostics. 2018 Sep 9;8(17):4795-4804. doi: 10.7150/thno.26093. eCollection 2018.

7.

Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men.

Chen H, Cade BE, Gleason KJ, Bjonnes AC, Stilp AM, Sofer T, Conomos MP, Ancoli-Israel S, Arens R, Azarbarzin A, Bell GI, Below JE, Chun S, Evans DS, Ewert R, Frazier-Wood AC, Gharib SA, Haba-Rubio J, Hagen EW, Heinzer R, Hillman DR, Johnson WC, Kutalik Z, Lane JM, Larkin EK, Lee SK, Liang J, Loredo JS, Mukherjee S, Palmer LJ, Papanicolaou GJ, Penzel T, Peppard PE, Post WS, Ramos AR, Rice K, Rotter JI, Sands SA, Shah NA, Shin C, Stone KL, Stubbe B, Sul JH, Tafti M, Taylor KD, Teumer A, Thornton TA, Tranah GJ, Wang C, Wang H, Warby SC, Wellman DA, Zee PC, Hanis CL, Laurie CC, Gottlieb DJ, Patel SR, Zhu X, Sunyaev SR, Saxena R, Lin X, Redline S.

Am J Respir Cell Mol Biol. 2018 Mar;58(3):391-401. doi: 10.1165/rcmb.2017-0237OC.

8.

Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes.

Duong D, Gai L, Snir S, Kang EY, Han B, Sul JH, Eskin E.

Bioinformatics. 2017 Jul 15;33(14):i67-i74. doi: 10.1093/bioinformatics/btx227.

9.

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.

Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, King RA, Dion Y, Rouleau G, Budman CL, Depienne C, Worbe Y, Hartmann A, Müller-Vahl KR, Stuhrmann M, Aschauer H, Stamenkovic M, Schloegelhofer M, Konstantinidis A, Lyon GJ, McMahon WM, Barta C, Tarnok Z, Nagy P, Batterson JR, Rizzo R, Cath DC, Wolanczyk T, Berlin C, Malaty IA, Okun MS, Woods DW, Rees E, Pato CN, Pato MT, Knowles JA, Posthuma D, Pauls DL, Cox NJ, Neale BM, Freimer NB, Paschou P, Mathews CA, Scharf JM, Coppola G; Tourette Syndrome Association International Consortium for Genetics (TSAICG); Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI).

Neuron. 2017 Jun 21;94(6):1101-1111.e7. doi: 10.1016/j.neuron.2017.06.010.

10.

Negative selection in humans and fruit flies involves synergistic epistasis.

Sohail M, Vakhrusheva OA, Sul JH, Pulit SL, Francioli LC; Genome of the Netherlands Consortium; Alzheimer’s Disease Neuroimaging Initiative, van den Berg LH, Veldink JH, de Bakker PIW, Bazykin GA, Kondrashov AS, Sunyaev SR.

Science. 2017 May 5;356(6337):539-542. doi: 10.1126/science.aah5238.

11.

Colocalization of GWAS and eQTL Signals Detects Target Genes.

Hormozdiari F, van de Bunt M, Segrè AV, Li X, Joo JWJ, Bilow M, Sul JH, Sankararaman S, Pasaniuc B, Eskin E.

Am J Hum Genet. 2016 Dec 1;99(6):1245-1260. doi: 10.1016/j.ajhg.2016.10.003. Epub 2016 Nov 17.

12.

Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.

Sul JH, Cade BE, Cho MH, Qiao D, Silverman EK, Redline S, Sunyaev S.

Am J Hum Genet. 2016 Oct 6;99(4):846-859. doi: 10.1016/j.ajhg.2016.08.015. Epub 2016 Sep 22.

13.

A genome-wide association analysis of chromosomal aberrations and Hirschsprung disease.

Bae JS, Koh I, Cheong HS, Seo JM, Kim DY, Oh JT, Kim HY, Jung K, Sul JH, Park WY, Kim JH, Shin HD.

Transl Res. 2016 Nov;177:31-40.e6. doi: 10.1016/j.trsl.2016.06.001. Epub 2016 Jun 14.

PMID:
27370899
14.

Using genomic annotations increases statistical power to detect eGenes.

Duong D, Zou J, Hormozdiari F, Sul JH, Ernst J, Han B, Eskin E.

Bioinformatics. 2016 Jun 15;32(12):i156-i163. doi: 10.1093/bioinformatics/btw272.

15.

Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models.

Sul JH, Bilow M, Yang WY, Kostem E, Furlotte N, He D, Eskin E.

PLoS Genet. 2016 Mar 4;12(3):e1005849. doi: 10.1371/journal.pgen.1005849. eCollection 2016 Mar.

16.

A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping.

Han B, Duong D, Sul JH, de Bakker PI, Eskin E, Raychaudhuri S.

Hum Mol Genet. 2016 May 1;25(9):1857-66. doi: 10.1093/hmg/ddw049. Epub 2016 Feb 21.

17.

Accurate and fast multiple-testing correction in eQTL studies.

Sul JH, Raj T, de Jong S, de Bakker PI, Raychaudhuri S, Ophoff RA, Stranger BE, Eskin E, Han B.

Am J Hum Genet. 2015 Jun 4;96(6):857-68. doi: 10.1016/j.ajhg.2015.04.012. Epub 2015 May 28.

18.

Gene-Gene Interactions Detection Using a Two-stage Model.

Wang Z, Sul JH, Snir S, Lozano JA, Eskin E.

J Comput Biol. 2015 Jun;22(6):563-76. doi: 10.1089/cmb.2014.0163. Epub 2015 Apr 14.

19.

Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma.

Luykx JJ, Bakker SC, Visser WF, Verhoeven-Duif N, Buizer-Voskamp JE, den Heijer JM, Boks MP, Sul JH, Eskin E, Ori AP, Cantor RM, Vorstman J, Strengman E, DeYoung J, Kappen TH, Pariama E, van Dongen EP, Borgdorff P, Bruins P, de Koning TJ, Kahn RS, Ophoff RA.

Mol Psychiatry. 2015 Dec;20(12):1557-64. doi: 10.1038/mp.2014.190. Epub 2015 Feb 10.

PMID:
25666758
20.

A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.

Kim JH, Cheong HS, Sul JH, Seo JM, Kim DY, Oh JT, Park KW, Kim HY, Jung SM, Jung K, Cho MJ, Bae JS, Shin HD.

PLoS One. 2014 Oct 13;9(10):e110292. doi: 10.1371/journal.pone.0110292. eCollection 2014.

21.

Characterization of genome-methylome interactions in 22 nuclear pedigrees.

Plongthongkum N, van Eijk KR, de Jong S, Wang T, Sul JH, Boks MP, Kahn RS, Fung HL, Ophoff RA, Zhang K.

PLoS One. 2014 Jul 14;9(7):e99313. doi: 10.1371/journal.pone.0099313. eCollection 2014.

22.

Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies.

Joo JW, Sul JH, Han B, Ye C, Eskin E.

Genome Biol. 2014 Apr 7;15(4):r61. doi: 10.1186/gb-2014-15-4-r61.

23.

Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches.

Sul JH, Han B, Ye C, Choi T, Eskin E.

PLoS Genet. 2013 Jun;9(6):e1003491. doi: 10.1371/journal.pgen.1003491. Epub 2013 Jun 13.

24.

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.

Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Westra HJ, Shakhbazov K, Abdellaoui A, Agrawal A, Albrecht E, Alizadeh BZ, Amin N, Barnard J, Baumeister SE, Benke KS, Bielak LF, Boatman JA, Boyle PA, Davies G, de Leeuw C, Eklund N, Evans DS, Ferhmann R, Fischer K, Gieger C, Gjessing HK, Hägg S, Harris JR, Hayward C, Holzapfel C, Ibrahim-Verbaas CA, Ingelsson E, Jacobsson B, Joshi PK, Jugessur A, Kaakinen M, Kanoni S, Karjalainen J, Kolcic I, Kristiansson K, Kutalik Z, Lahti J, Lee SH, Lin P, Lind PA, Liu Y, Lohman K, Loitfelder M, McMahon G, Vidal PM, Meirelles O, Milani L, Myhre R, Nuotio ML, Oldmeadow CJ, Petrovic KE, Peyrot WJ, Polasek O, Quaye L, Reinmaa E, Rice JP, Rizzi TS, Schmidt H, Schmidt R, Smith AV, Smith JA, Tanaka T, Terracciano A, van der Loos MJ, Vitart V, Völzke H, Wellmann J, Yu L, Zhao W, Allik J, Attia JR, Bandinelli S, Bastardot F, Beauchamp J, Bennett DA, Berger K, Bierut LJ, Boomsma DI, Bültmann U, Campbell H, Chabris CF, Cherkas L, Chung MK, Cucca F, de Andrade M, De Jager PL, De Neve JE, Deary IJ, Dedoussis GV, Deloukas P, Dimitriou M, Eiríksdóttir G, Elderson MF, Eriksson JG, Evans DM, Faul JD, Ferrucci L, Garcia ME, Grönberg H, Guðnason V, Hall P, Harris JM, Harris TB, Hastie ND, Heath AC, Hernandez DG, Hoffmann W, Hofman A, Holle R, Holliday EG, Hottenga JJ, Iacono WG, Illig T, Järvelin MR, Kähönen M, Kaprio J, Kirkpatrick RM, Kowgier M, Latvala A, Launer LJ, Lawlor DA, Lehtimäki T, Li J, Lichtenstein P, Lichtner P, Liewald DC, Madden PA, Magnusson PK, Mäkinen TE, Masala M, McGue M, Metspalu A, Mielck A, Miller MB, Montgomery GW, Mukherjee S, Nyholt DR, Oostra BA, Palmer LJ, Palotie A, Penninx BW, Perola M, Peyser PA, Preisig M, Räikkönen K, Raitakari OT, Realo A, Ring SM, Ripatti S, Rivadeneira F, Rudan I, Rustichini A, Salomaa V, Sarin AP, Schlessinger D, Scott RJ, Snieder H, St Pourcain B, Starr JM, Sul JH, Surakka I, Svento R, Teumer A; LifeLines Cohort Study, Tiemeier H, van Rooij FJ, Van Wagoner DR, Vartiainen E, Viikari J, Vollenweider P, Vonk JM, Waeber G, Weir DR, Wichmann HE, Widen E, Willemsen G, Wilson JF, Wright AF, Conley D, Davey-Smith G, Franke L, Groenen PJ, Hofman A, Johannesson M, Kardia SL, Krueger RF, Laibson D, Martin NG, Meyer MN, Posthuma D, Thurik AR, Timpson NJ, Uitterlinden AG, van Duijn CM, Visscher PM, Benjamin DJ, Cesarini D, Koellinger PD.

Science. 2013 Jun 21;340(6139):1467-71. doi: 10.1126/science.1235488. Epub 2013 May 30.

25.

Rare variant association testing under low-coverage sequencing.

Navon O, Sul JH, Han B, Conde L, Bracci PM, Riby J, Skibola CF, Eskin E, Halperin E.

Genetics. 2013 Jul;194(3):769-79. doi: 10.1534/genetics.113.150169. Epub 2013 May 1.

26.

Mixed models can correct for population structure for genomic regions under selection.

Sul JH, Eskin E.

Nat Rev Genet. 2013 Apr;14(4):300. doi: 10.1038/nrg2813-c1. Epub 2013 Feb 26. No abstract available.

PMID:
23438871
27.

The Minnesota Center for Twin and Family Research genome-wide association study.

Miller MB, Basu S, Cunningham J, Eskin E, Malone SM, Oetting WS, Schork N, Sul JH, Iacono WG, McGue M.

Twin Res Hum Genet. 2012 Dec;15(6):767-74. doi: 10.1017/thg.2012.62.

28.

Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.

Luykx JJ, Bakker SC, Lentjes E, Neeleman M, Strengman E, Mentink L, DeYoung J, de Jong S, Sul JH, Eskin E, van Eijk K, van Setten J, Buizer-Voskamp JE, Cantor RM, Lu A, van Amerongen M, van Dongen EP, Keijzers P, Kappen T, Borgdorff P, Bruins P, Derks EM, Kahn RS, Ophoff RA.

Mol Psychiatry. 2014 Feb;19(2):228-34. doi: 10.1038/mp.2012.183. Epub 2013 Jan 15.

PMID:
23319000
29.

Impact of pressure load caused by right ventricular outflow tract obstruction on right ventricular volume overload in patients with repaired tetralogy of Fallot.

Yoo BW, Kim JO, Kim YJ, Choi JY, Park HK, Park YH, Sul JH.

J Thorac Cardiovasc Surg. 2012 Jun;143(6):1299-304. doi: 10.1016/j.jtcvs.2011.12.033. Epub 2012 Jan 12.

30.

Increasing power of groupwise association test with likelihood ratio test.

Sul JH, Han B, Eskin E.

J Comput Biol. 2011 Nov;18(11):1611-24. doi: 10.1089/cmb.2011.0161. Epub 2011 Sep 15.

31.

Role of rodent secondary motor cortex in value-based action selection.

Sul JH, Jo S, Lee D, Jung MW.

Nat Neurosci. 2011 Aug 14;14(9):1202-8. doi: 10.1038/nn.2881. Erratum in: Nat Neurosci. 2013 Dec;16(12):1906.

32.

Implanted bone marrow-derived mesenchymal stem cells fail to metabolically stabilize or recover electromechanical function in infarcted hearts.

Eun LY, Song H, Choi E, Lee TG, Moon DW, Hwang D, Byun KH, Sul JH, Hwang KC.

Tissue Cell. 2011 Aug;43(4):238-45. doi: 10.1016/j.tice.2011.04.002. Epub 2011 Jun 22.

PMID:
21700305
33.

Traumatic ventricular septal defect in a 4-year-old boy after blunt chest injury.

Kim YM, Yoo BW, Choi JY, Sul JH, Park YH.

Korean J Pediatr. 2011 Feb;54(2):86-9. doi: 10.3345/kjp.2011.54.2.86. Epub 2011 Feb 28.

34.

An optimal weighted aggregated association test for identification of rare variants involved in common diseases.

Sul JH, Han B, He D, Eskin E.

Genetics. 2011 May;188(1):181-8. doi: 10.1534/genetics.110.125070. Epub 2011 Mar 2.

35.

Clinical outcome of transcatheter closure of patent ductus arteriosus in small children weighing 10 kg or less.

Park YA, Kim NK, Park SJ, Yun BS, Choi JY, Sul JH.

Korean J Pediatr. 2010 Dec;53(12):1012-7. doi: 10.3345/kjp.2010.53.12.1012. Epub 2010 Dec 31.

36.

Distinct roles of rodent orbitofrontal and medial prefrontal cortex in decision making.

Sul JH, Kim H, Huh N, Lee D, Jung MW.

Neuron. 2010 May 13;66(3):449-60. doi: 10.1016/j.neuron.2010.03.033.

37.

Morphologic Characteristics and Relating Factors to the Need of Technical Modification in Transcatheter Closure of Large Atrial Septal Defect (>/=25 mm).

Park SJ, Kim NK, Kim JO, Yoo BW, Choi JY, Sul JH.

Korean Circ J. 2010 Apr;40(4):191-6. doi: 10.4070/kcj.2010.40.4.191. Epub 2010 Apr 22.

38.

Variance component model to account for sample structure in genome-wide association studies.

Kang HM, Sul JH, Service SK, Zaitlen NA, Kong SY, Freimer NB, Sabatti C, Eskin E.

Nat Genet. 2010 Apr;42(4):348-54. doi: 10.1038/ng.548. Epub 2010 Mar 7.

39.

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.

Stein JL, Hua X, Morra JH, Lee S, Hibar DP, Ho AJ, Leow AD, Toga AW, Sul JH, Kang HM, Eskin E, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, Allen AN, Corneveaux JJ, Stephan DA, Webster J, DeChairo BM, Potkin SG, Jack CR Jr, Weiner MW, Thompson PM; Alzheimer's Disease Neuroimaging Initiative.

Neuroimage. 2010 Jun;51(2):542-54. doi: 10.1016/j.neuroimage.2010.02.068. Epub 2010 Mar 1.

40.

Role of striatum in updating values of chosen actions.

Kim H, Sul JH, Huh N, Lee D, Jung MW.

J Neurosci. 2009 Nov 25;29(47):14701-12. doi: 10.1523/JNEUROSCI.2728-09.2009.

41.

Model-based reinforcement learning under concurrent schedules of reinforcement in rodents.

Huh N, Jo S, Kim H, Sul JH, Jung MW.

Learn Mem. 2009 Apr 29;16(5):315-23. doi: 10.1101/lm.1295509. Print 2009 May.

PMID:
19403794
42.

Polytetrafluoroethylene-covered stent deployment in the setting of Kawasaki disease.

Kwon HS, Shin JI, Choi JY, Sul JH, Jang YS.

Catheter Cardiovasc Interv. 2007 Jun 1;69(7):1075-6; author reply 1077. No abstract available.

PMID:
17526008
43.

Right ventricular restrictive physiology in repaired tetralogy of Fallot is associated with smaller respiratory variability.

Choi JY, Kwon HS, Yoo BW, Shin JI, Sul JH, Park HK, Park YH.

Int J Cardiol. 2008 Mar 28;125(1):28-35. Epub 2007 Apr 12.

PMID:
17433839
44.

Cardiac manifestations of Henoch-Schoenlein purpura: IgA mediated vasculitis or Rheumatic fever?

Shin JI, Kim JH, Lee JS, Kim DS, Choi JY, Sul JH.

Eur J Pediatr. 2007 Jun;166(6):627. Epub 2006 Sep 19. No abstract available.

PMID:
17047991
45.

Dietary mineral and trace element intake and squamous cell carcinoma of the esophagus in a Chinese population.

Lu H, Cai L, Mu LN, Lu QY, Zhao J, Cui Y, Sul JH, Zhou XF, Ding BG, Elashoff RM, Marshall J, Yu SZ, Jiang QW, Zhang ZF.

Nutr Cancer. 2006;55(1):63-70.

PMID:
16965242
46.

Kawasaki disease and hyponatremia.

Shin JI, Kim JH, Lee JS, Kim DS, Choi JY, Sul JH.

Pediatr Nephrol. 2006 Oct;21(10):1490-1; author reply 1492. Epub 2006 Aug 8. No abstract available.

PMID:
16896998
47.

Rapidly progressive dilatation of coronary artery aneurysm associated with Kawasaki disease.

Shin JI, Choi JY, Sul JH, Kim DS, Park YH.

Eur J Pediatr. 2007 Jan;166(1):87; author reply 89-90; discussion 91. Epub 2006 Jul 22. No abstract available.

PMID:
16862436
48.

The effects of weight load and joint immobilization on reorganization of postural tremor.

Hwang IS, Huang CC, Sul JH, Huang CT, Wang CH, Young MS.

Electromyogr Clin Neurophysiol. 2006 Mar-Apr;46(2):67-77.

PMID:
16795996
49.

Mapping subsets of scholarly information.

Ginsparg P, Houle P, Joachims T, Sul JH.

Proc Natl Acad Sci U S A. 2004 Apr 6;101 Suppl 1:5236-40. Epub 2004 Feb 6.

50.

Using electron beam CT to evaluate conotruncal anomalies in pediatric and adult patients.

Choi BW, Park YH, Choi JY, Choi BI, Kim MJ, Ryu SJ, Lee JK, Sul JH, Lee SK, Cho BK, Choe KO.

AJR Am J Roentgenol. 2001 Nov;177(5):1045-9. No abstract available.

PMID:
11641166

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