Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 112

1.

Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review.

Fatkin D, Huttner IG, Kovacic JC, Seidman JG, Seidman CE.

J Am Coll Cardiol. 2019 Dec 10;74(23):2921-2938. doi: 10.1016/j.jacc.2019.10.011. Review.

PMID:
31806137
2.

Genetics of atrial cardiomyopathy.

Fatkin D, Huttner IG, Johnson R.

Curr Opin Cardiol. 2019 May;34(3):275-281. doi: 10.1097/HCO.0000000000000610.

PMID:
30672791
3.

Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection.

Adlam D, Olson TM, Combaret N, Kovacic JC, Iismaa SE, Al-Hussaini A, O'Byrne MM, Bouajila S, Georges A, Mishra K, Braund PS, d'Escamard V, Huang S, Margaritis M, Nelson CP, de Andrade M, Kadian-Dodov D, Welch CA, Mazurkiewicz S, Jeunemaitre X; DISCO Consortium, Wong CMY, Giannoulatou E, Sweeting M, Muller D, Wood A, McGrath-Cadell L, Fatkin D, Dunwoodie SL, Harvey R, Holloway C, Empana JP, Jouven X; CARDIoGRAMPlusC4D Study Group, Olin JW, Gulati R, Tweet MS, Hayes SN, Samani NJ, Graham RM, Motreff P, Bouatia-Naji N.

J Am Coll Cardiol. 2019 Jan 8;73(1):58-66. doi: 10.1016/j.jacc.2018.09.085.

PMID:
30621952
4.

Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management.

Peters S, Kumar S, Elliott P, Kalman JM, Fatkin D.

Heart Lung Circ. 2019 Jan;28(1):31-38. doi: 10.1016/j.hlc.2018.09.010. Epub 2018 Oct 11. Review.

PMID:
30482687
5.

ETV1: A New Player in Atrial Remodeling.

Fatkin D.

Circ Res. 2018 Aug 17;123(5):515-517. doi: 10.1161/CIRCRESAHA.118.313606. No abstract available.

PMID:
30355145
6.

A-Band Titin Truncation in Zebrafish Causes Dilated Cardiomyopathy and Hemodynamic Stress Intolerance.

Huttner IG, Wang LW, Santiago CF, Horvat C, Johnson R, Cheng D, von Frieling-Salewsky M, Hillcoat K, Bemand TJ, Trivedi G, Braet F, Hesselson D, Alford K, Hayward CS, Seidman JG, Seidman CE, Feneley MP, Linke WA, Fatkin D.

Circ Genom Precis Med. 2018 Aug;11(8):e002135. doi: 10.1161/CIRCGEN.118.002135.

PMID:
30354343
7.

Response to Brodehl et al.

Minoche AE, Horvat C, Johnson R, Gayevskiy V, Morton SU, Drew AP, Woo K, Statham AL, Lundie B, Bagnall RD, Ingles J, Semsarian C, Seidman JG, Seidman CE, Dinger ME, Cowley MJ, Fatkin D.

Genet Med. 2019 May;21(5):1248-1249. doi: 10.1038/s41436-018-0292-1. Epub 2018 Sep 28. No abstract available.

PMID:
30262924
8.

Endocardial TRPC-6 Channels Act as Atrial Mechanosensors and Load-Dependent Modulators of Endocardial/Myocardial Cross-Talk.

Nikolova-Krstevski V, Wagner S, Yu ZY, Cox CD, Cvetkovska J, Hill AP, Huttner IG, Benson V, Werdich AA, MacRae C, Feneley MP, Friedrich O, Martinac B, Fatkin D.

JACC Basic Transl Sci. 2017 Oct 30;2(5):575-590. doi: 10.1016/j.jacbts.2017.05.006. eCollection 2017 Oct.

9.

Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.

Bagnall RD, Ingles J, Dinger ME, Cowley MJ, Ross SB, Minoche AE, Lal S, Turner C, Colley A, Rajagopalan S, Berman Y, Ronan A, Fatkin D, Semsarian C.

J Am Coll Cardiol. 2018 Jul 24;72(4):419-429. doi: 10.1016/j.jacc.2018.04.078.

10.

A Langendorff-like system to quantify cardiac pump function in adult zebrafish.

Zhang H, Dvornikov AV, Huttner IG, Ma X, Santiago CF, Fatkin D, Xu X.

Dis Model Mech. 2018 Sep 10;11(9). pii: dmm034819. doi: 10.1242/dmm.034819.

11.

Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.

Minoche AE, Horvat C, Johnson R, Gayevskiy V, Morton SU, Drew AP, Woo K, Statham AL, Lundie B, Bagnall RD, Ingles J, Semsarian C, Seidman JG, Seidman CE, Dinger ME, Cowley MJ, Fatkin D.

Genet Med. 2019 Mar;21(3):650-662. doi: 10.1038/s41436-018-0084-7. Epub 2018 Jul 2.

PMID:
29961767
12.

A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy.

Horvat C, Johnson R, Lam L, Munro J, Mazzarotto F, Roberts AM, Herman DS, Parfenov M, Haghighi A, McDonough B, DePalma SR, Keogh AM, Macdonald PS, Hayward CS, Roberts A, Barton PJR, Felkin LE, Giannoulatou E, Cook SA, Seidman JG, Seidman CE, Fatkin D.

Genet Med. 2019 Jan;21(1):133-143. doi: 10.1038/s41436-018-0036-2. Epub 2018 Jun 11.

13.

Multi-ethnic genome-wide association study for atrial fibrillation.

Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, Bis JC, Bloom HL, Boerwinkle E, Bottinger EB, Brody JA, Calkins H, Campbell A, Cappola TP, Carlquist J, Chasman DI, Chen LY, Chen YI, Choi EK, Choi SH, Christophersen IE, Chung MK, Cole JW, Conen D, Cook J, Crijns HJ, Cutler MJ, Damrauer SM, Daniels BR, Darbar D, Delgado G, Denny JC, Dichgans M, Dörr M, Dudink EA, Dudley SC, Esa N, Esko T, Eskola M, Fatkin D, Felix SB, Ford I, Franco OH, Geelhoed B, Grewal RP, Gudnason V, Guo X, Gupta N, Gustafsson S, Gutmann R, Hamsten A, Harris TB, Hayward C, Heckbert SR, Hernesniemi J, Hocking LJ, Hofman A, Horimoto ARVR, Huang J, Huang PL, Huffman J, Ingelsson E, Ipek EG, Ito K, Jimenez-Conde J, Johnson R, Jukema JW, Kääb S, Kähönen M, Kamatani Y, Kane JP, Kastrati A, Kathiresan S, Katschnig-Winter P, Kavousi M, Kessler T, Kietselaer BL, Kirchhof P, Kleber ME, Knight S, Krieger JE, Kubo M, Launer LJ, Laurikka J, Lehtimäki T, Leineweber K, Lemaitre RN, Li M, Lim HE, Lin HJ, Lin H, Lind L, Lindgren CM, Lokki ML, London B, Loos RJF, Low SK, Lu Y, Lyytikäinen LP, Macfarlane PW, Magnusson PK, Mahajan A, Malik R, Mansur AJ, Marcus GM, Margolin L, Margulies KB, März W, McManus DD, Melander O, Mohanty S, Montgomery JA, Morley MP, Morris AP, Müller-Nurasyid M, Natale A, Nazarian S, Neumann B, Newton-Cheh C, Niemeijer MN, Nikus K, Nilsson P, Noordam R, Oellers H, Olesen MS, Orho-Melander M, Padmanabhan S, Pak HN, Paré G, Pedersen NL, Pera J, Pereira A, Porteous D, Psaty BM, Pulit SL, Pullinger CR, Rader DJ, Refsgaard L, Ribasés M, Ridker PM, Rienstra M, Risch L, Roden DM, Rosand J, Rosenberg MA, Rost N, Rotter JI, Saba S, Sandhu RK, Schnabel RB, Schramm K, Schunkert H, Schurman C, Scott SA, Seppälä I, Shaffer C, Shah S, Shalaby AA, Shim J, Shoemaker MB, Siland JE, Sinisalo J, Sinner MF, Slowik A, Smith AV, Smith BH, Smith JG, Smith JD, Smith NL, Soliman EZ, Sotoodehnia N, Stricker BH, Sun A, Sun H, Svendsen JH, Tanaka T, Tanriverdi K, Taylor KD, Teder-Laving M, Teumer A, Thériault S, Trompet S, Tucker NR, Tveit A, Uitterlinden AG, Van Der Harst P, Van Gelder IC, Van Wagoner DR, Verweij N, Vlachopoulou E, Völker U, Wang B, Weeke PE, Weijs B, Weiss R, Weiss S, Wells QS, Wiggins KL, Wong JA, Woo D, Worrall BB, Yang PS, Yao J, Yoneda ZT, Zeller T, Zeng L, Lubitz SA, Lunetta KL, Ellinor PT.

Nat Genet. 2018 Jun 11;50(9):1225-1233. doi: 10.1038/s41588-018-0133-9.

14.

Is There a Role for Genes in Exercise-Induced Atrial Cardiomyopathy?

Fatkin D, Cox CD, Huttner IG, Martinac B.

Heart Lung Circ. 2018 Sep;27(9):1093-1098. doi: 10.1016/j.hlc.2018.03.028. Epub 2018 Apr 9. Review.

PMID:
29706494
15.

Left Ventricular Diastolic Dysfunction in Hutchinson-Gilford Progeria Syndrome.

Fatkin D.

JAMA Cardiol. 2018 Apr 1;3(4):334-335. doi: 10.1001/jamacardio.2017.5377. No abstract available.

PMID:
29466548
16.

High-Frequency Echocardiography - Transformative Clinical and Research Applications in Humans, Mice, and Zebrafish.

Wang LW, Kesteven SH, Huttner IG, Feneley MP, Fatkin D.

Circ J. 2018 Feb 23;82(3):620-628. doi: 10.1253/circj.CJ-18-0027. Epub 2018 Feb 6. Review.

17.

Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.

Ito K, Patel PN, Gorham JM, McDonough B, DePalma SR, Adler EE, Lam L, MacRae CA, Mohiuddin SM, Fatkin D, Seidman CE, Seidman JG.

Proc Natl Acad Sci U S A. 2017 Jul 18;114(29):7689-7694. doi: 10.1073/pnas.1707741114. Epub 2017 Jul 5.

18.

Position Statement on the Diagnosis and Management of Familial Dilated Cardiomyopathy.

Fatkin D, Johnson R, McGaughran J, Weintraub RG, Atherton JJ; CSANZ Genetics Council Writing Group.

Heart Lung Circ. 2017 Nov;26(11):1127-1132. doi: 10.1016/j.hlc.2017.04.021. Epub 2017 Jun 7. No abstract available.

PMID:
28655534
19.

Adding dimension to cellular mechanotransduction: Advances in biomedical engineering of multiaxial cell-stretch systems and their application to cardiovascular biomechanics and mechano-signaling.

Friedrich O, Schneidereit D, Nikolaev YA, Nikolova-Krstevski V, Schürmann S, Wirth-Hücking A, Merten AL, Fatkin D, Martinac B.

Prog Biophys Mol Biol. 2017 Nov;130(Pt B):170-191. doi: 10.1016/j.pbiomolbio.2017.06.011. Epub 2017 Jun 21. Review.

PMID:
28647645
20.

Genetics of Atrial Fibrillation: State of the Art in 2017.

Fatkin D, Santiago CF, Huttner IG, Lubitz SA, Ellinor PT.

Heart Lung Circ. 2017 Sep;26(9):894-901. doi: 10.1016/j.hlc.2017.04.008. Epub 2017 May 11. Review.

PMID:
28601532
21.

Are Double Mutations Double Trouble?

Fatkin D, Johnson R.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001749. doi: 10.1161/CIRCGENETICS.117.001749. No abstract available.

PMID:
28420667
22.

Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling.

Furtado MB, Wilmanns JC, Chandran A, Perera J, Hon O, Biben C, Willow TJ, Nim HT, Kaur G, Simonds S, Wu Q, Willians D, Salimova E, Plachta N, Denegre JM, Murray SA, Fatkin D, Cowley M, Pearson JT, Kaye D, Ramialison M, Harvey RP, Rosenthal NA, Costa MW.

JCI Insight. 2017 Mar 23;2(6):e88271. doi: 10.1172/jci.insight.88271.

23.

Titin-truncating mutations in dilated cardiomyopathy: the long and short of it.

Fatkin D, Huttner IG.

Curr Opin Cardiol. 2017 Feb 1. doi: 10.1097/HCO.0000000000000382. [Epub ahead of print]

PMID:
28151760
24.

Standardized echocardiographic assessment of cardiac function in normal adult zebrafish and heart disease models.

Wang LW, Huttner IG, Santiago CF, Kesteven SH, Yu ZY, Feneley MP, Fatkin D.

Dis Model Mech. 2017 Jan 1;10(1):63-76. doi: 10.1242/dmm.026989. Epub 2016 Dec 20.

25.

Bradycardia in Zebrafish Heart Failure: A True Physiological Response or Anesthetic-Induced Red Herring?

Wang LW, Huttner IG, Santiago CF, Fatkin D.

Zebrafish. 2016 Dec;13(6):475-476. Epub 2016 Sep 27. No abstract available.

PMID:
27676282
26.

Contextualizing Genetics for Regional Heart Failure Care.

Iyngkaran P, Thomas MC, Johnson R, French J, Ilton M, McDonald P, Hare DL, Fatkin D.

Curr Cardiol Rev. 2016;12(3):231-42. Review.

27.

The two-pore domain potassium channel, TWIK-1, has a role in the regulation of heart rate and atrial size.

Christensen AH, Chatelain FC, Huttner IG, Olesen MS, Soka M, Feliciangeli S, Horvat C, Santiago CF, Vandenberg JI, Schmitt N, Olesen SP, Lesage F, Fatkin D.

J Mol Cell Cardiol. 2016 Aug;97:24-35. doi: 10.1016/j.yjmcc.2016.04.006. Epub 2016 Apr 19.

PMID:
27103460
28.

Snowflakes in the heart: an ultrasonic marker of severe hypercoagulability.

Wang LW, Grygiel JJ, O'Neill JH, Fatkin D, Feneley MP.

Lancet. 2015 Jan 17;385(9964):302. doi: 10.1016/S0140-6736(14)62221-2. No abstract available.

PMID:
25706710
29.

Irreversible triggers for hypertrophic cardiomyopathy are established in the early postnatal period.

Cannon L, Yu ZY, Marciniec T, Waardenberg AJ, Iismaa SE, Nikolova-Krstevski V, Neist E, Ohanian M, Qiu MR, Rainer S, Harvey RP, Feneley MP, Graham RM, Fatkin D.

J Am Coll Cardiol. 2015 Feb 17;65(6):560-9. doi: 10.1016/j.jacc.2014.10.069.

30.

Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.

Roberts AM, Ware JS, Herman DS, Schafer S, Baksi J, Bick AG, Buchan RJ, Walsh R, John S, Wilkinson S, Mazzarotto F, Felkin LE, Gong S, MacArthur JA, Cunningham F, Flannick J, Gabriel SB, Altshuler DM, Macdonald PS, Heinig M, Keogh AM, Hayward CS, Banner NR, Pennell DJ, O'Regan DP, San TR, de Marvao A, Dawes TJ, Gulati A, Birks EJ, Yacoub MH, Radke M, Gotthardt M, Wilson JG, O'Donnell CJ, Prasad SK, Barton PJ, Fatkin D, Hubner N, Seidman JG, Seidman CE, Cook SA.

Sci Transl Med. 2015 Jan 14;7(270):270ra6. doi: 10.1126/scitranslmed.3010134.

31.

RhoA/ROCK signaling and pleiotropic α1A-adrenergic receptor regulation of cardiac contractility.

Yu ZY, Tan JC, McMahon AC, Iismaa SE, Xiao XH, Kesteven SH, Reichelt ME, Mohl MC, Smith NJ, Fatkin D, Allen D, Head SI, Graham RM, Feneley MP.

PLoS One. 2014 Jun 11;9(6):e99024. doi: 10.1371/journal.pone.0099024. eCollection 2014.

32.

Candidate disease gene prediction using Gentrepid: application to a genome-wide association study on coronary artery disease.

Ballouz S, Liu JY, Oti M, Gaeta B, Fatkin D, Bahlo M, Wouters MA.

Mol Genet Genomic Med. 2014 Jan;2(1):44-57. doi: 10.1002/mgg3.40. Epub 2013 Nov 13.

33.

Genetics and disease of ventricular muscle.

Fatkin D, Seidman CE, Seidman JG.

Cold Spring Harb Perspect Med. 2014 Jan 1;4(1):a021063. doi: 10.1101/cshperspect.a021063. Review.

34.

Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis.

Liang B, Soka M, Christensen AH, Olesen MS, Larsen AP, Knop FK, Wang F, Nielsen JB, Andersen MN, Humphreys D, Mann SA, Huttner IG, Vandenberg JI, Svendsen JH, Haunsø S, Preiss T, Seebohm G, Olesen SP, Schmitt N, Fatkin D.

J Mol Cell Cardiol. 2014 Feb;67:69-76. doi: 10.1016/j.yjmcc.2013.12.014. Epub 2013 Dec 27.

PMID:
24374141
35.

Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.

Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, Blom N, Brugada J, Chiang CE, Huikuri H, Kannankeril P, Krahn A, Leenhardt A, Moss A, Schwartz PJ, Shimizu W, Tomaselli G, Tracy C; Document Reviewers, Ackerman M, Belhassen B, Estes NA 3rd, Fatkin D, Kalman J, Kaufman E, Kirchhof P, Schulze-Bahr E, Wolpert C, Vohra J, Refaat M, Etheridge SP, Campbell RM, Martin ET, Quek SC; Heart Rhythm Society; European Heart Rhythm Association; Asia Pacific Heart Rhythm Society.

Europace. 2013 Oct;15(10):1389-406. doi: 10.1093/europace/eut272. Epub 2013 Aug 30. Review. No abstract available.

PMID:
23994779
36.

Gentrepid V2.0: a web server for candidate disease gene prediction.

Ballouz S, Liu JY, George RA, Bains N, Liu A, Oti M, Gaeta B, Fatkin D, Wouters MA.

BMC Bioinformatics. 2013 Aug 16;14:249. doi: 10.1186/1471-2105-14-249.

37.

Efficacy of carvedilol in pediatric heart failure.

Christensen AH, Fatkin D.

Future Cardiol. 2013 Jul;9(4):475-8. doi: 10.2217/fca.13.36.

PMID:
23834688
38.

A transgenic zebrafish model of a human cardiac sodium channel mutation exhibits bradycardia, conduction-system abnormalities and early death.

Huttner IG, Trivedi G, Jacoby A, Mann SA, Vandenberg JI, Fatkin D.

J Mol Cell Cardiol. 2013 Aug;61:123-32. doi: 10.1016/j.yjmcc.2013.06.005. Epub 2013 Jun 19.

PMID:
23791817
39.

Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy.

Costa MW, Guo G, Wolstein O, Vale M, Castro ML, Wang L, Otway R, Riek P, Cochrane N, Furtado M, Semsarian C, Weintraub RG, Yeoh T, Hayward C, Keogh A, Macdonald P, Feneley M, Graham RM, Seidman JG, Seidman CE, Rosenthal N, Fatkin D, Harvey RP.

Circ Cardiovasc Genet. 2013 Jun;6(3):238-47. doi: 10.1161/CIRCGENETICS.113.000057. Epub 2013 May 9.

40.

A heterozygous variant in the human cardiac miR-133 gene, MIR133A2, alters miRNA duplex processing and strand abundance.

Ohanian M, Humphreys DT, Anderson E, Preiss T, Fatkin D.

BMC Genet. 2013 Mar 6;14:18. doi: 10.1186/1471-2156-14-18.

41.

Atrial cardiomyopathy an orphan disease or common disorder?

Fatkin D, Nikolova-Krstevski V.

Circ Cardiovasc Genet. 2013 Feb;6(1):5-6. doi: 10.1161/CIRCGENETICS.111.000033. No abstract available.

PMID:
23424254
42.

Heuristic methods for finding pathogenic variants in gene coding sequences.

Ohanian M, Otway R, Fatkin D.

J Am Heart Assoc. 2012 Oct;1(5):e002642. doi: 10.1161/JAHA.112.002642. Epub 2012 Oct 25. Review. No abstract available.

43.

R222Q SCN5A mutation is associated with reversible ventricular ectopy and dilated cardiomyopathy.

Mann SA, Castro ML, Ohanian M, Guo G, Zodgekar P, Sheu A, Stockhammer K, Thompson T, Playford D, Subbiah R, Kuchar D, Aggarwal A, Vandenberg JI, Fatkin D.

J Am Coll Cardiol. 2012 Oct 16;60(16):1566-73. doi: 10.1016/j.jacc.2012.05.050. Epub 2012 Sep 19.

44.

Pathways of Ca²⁺ entry and cytoskeletal damage following eccentric contractions in mouse skeletal muscle.

Zhang BT, Whitehead NP, Gervasio OL, Reardon TF, Vale M, Fatkin D, Dietrich A, Yeung EW, Allen DG.

J Appl Physiol (1985). 2012 Jun;112(12):2077-86. doi: 10.1152/japplphysiol.00770.2011. Epub 2012 Mar 29.

45.

Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk.

Mann SA, Otway R, Guo G, Soka M, Karlsdotter L, Trivedi G, Ohanian M, Zodgekar P, Smith RA, Wouters MA, Subbiah R, Walker B, Kuchar D, Sanders P, Griffiths L, Vandenberg JI, Fatkin D.

J Am Coll Cardiol. 2012 Mar 13;59(11):1017-25. doi: 10.1016/j.jacc.2011.11.039.

46.

Complexity of murine cardiomyocyte miRNA biogenesis, sequence variant expression and function.

Humphreys DT, Hynes CJ, Patel HR, Wei GH, Cannon L, Fatkin D, Suter CM, Clancy JL, Preiss T.

PLoS One. 2012;7(2):e30933. doi: 10.1371/journal.pone.0030933. Epub 2012 Feb 3.

47.

Familial dilated cardiomyopathy: Current challenges and future directions.

Fatkin D.

Glob Cardiol Sci Pract. 2012 Aug 27;2012(1):8. doi: 10.5339/gcsp.2012.8. eCollection 2012. Review. No abstract available.

48.

Role of the nuclear envelope in the pathogenesis of age-related bone loss and osteoporosis.

Vidal C, Bermeo S, Fatkin D, Duque G.

Bonekey Rep. 2012 May 2;1:62. doi: 10.1038/bonekey.2012.62. eCollection 2012.

49.

Analysis of genome-wide association study data using the protein knowledge base.

Ballouz S, Liu JY, Oti M, Gaeta B, Fatkin D, Bahlo M, Wouters MA.

BMC Genet. 2011 Nov 13;12:98. doi: 10.1186/1471-2156-12-98.

50.

Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations.

Granados-Riveron JT, Pope M, Bu'lock FA, Thornborough C, Eason J, Setchfield K, Ketley A, Kirk EP, Fatkin D, Feneley MP, Harvey RP, Brook JD.

Congenit Heart Dis. 2012 Mar-Apr;7(2):151-9. doi: 10.1111/j.1747-0803.2011.00573.x. Epub 2011 Oct 20.

Supplemental Content

Loading ...
Support Center