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Year Number of Results
1990 1
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1998 1
2000 6
2001 3
2002 2
2003 1
2004 2
2005 7
2006 8
2007 7
2008 3
2009 2
2010 4
2011 9
2012 7
2013 11
2014 8
2015 2
2016 9
2017 2
2018 12
2019 18
2020 14
2021 21
2022 15
2023 7
2024 9
2025 15

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187 results

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Page 1
Onasemnogene abeparvovec for presymptomatic infants with three copies of SMN2 at risk for spinal muscular atrophy: the Phase III SPR1NT trial.
Strauss KA, Farrar MA, Muntoni F, Saito K, Mendell JR, Servais L, McMillan HJ, Finkel RS, Swoboda KJ, Kwon JM, Zaidman CM, Chiriboga CA, Iannaccone ST, Krueger JM, Parsons JA, Shieh PB, Kavanagh S, Wigderson M, Tauscher-Wisniewski S, McGill BE, Macek TA. Strauss KA, et al. Among authors: kwon jm. Nat Med. 2022 Jul;28(7):1390-1397. doi: 10.1038/s41591-022-01867-3. Epub 2022 Jun 17. Nat Med. 2022. PMID: 35715567 Free PMC article. Clinical Trial.
Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy in patients with two copies of SMN2 (STR1VE): an open-label, single-arm, multicentre, phase 3 trial.
Day JW, Finkel RS, Chiriboga CA, Connolly AM, Crawford TO, Darras BT, Iannaccone ST, Kuntz NL, Peña LDM, Shieh PB, Smith EC, Kwon JM, Zaidman CM, Schultz M, Feltner DE, Tauscher-Wisniewski S, Ouyang H, Chand DH, Sproule DM, Macek TA, Mendell JR. Day JW, et al. Among authors: kwon jm. Lancet Neurol. 2021 Apr;20(4):284-293. doi: 10.1016/S1474-4422(21)00001-6. Epub 2021 Mar 17. Lancet Neurol. 2021. PMID: 33743238 Clinical Trial.
Newborn screening for Krabbe disease in New York State: the first eight years' experience.
Orsini JJ, Kay DM, Saavedra-Matiz CA, Wenger DA, Duffner PK, Erbe RW, Biski C, Martin M, Krein LM, Nichols M, Kurtzberg J, Escolar ML, Adams DJ, Arnold GL, Iglesias A, Galvin-Parton P, Kronn DF, Kwon JM, Levy PA, Pellegrino JE, Shur N, Wasserstein MP, Caggana M; New York State Krabbe Disease Consortium. Orsini JJ, et al. Among authors: kwon jm. Genet Med. 2016 Mar;18(3):239-48. doi: 10.1038/gim.2015.211. Epub 2016 Jan 21. Genet Med. 2016. PMID: 26795590 Free article.
Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trial.
Strauss KA, Farrar MA, Muntoni F, Saito K, Mendell JR, Servais L, McMillan HJ, Finkel RS, Swoboda KJ, Kwon JM, Zaidman CM, Chiriboga CA, Iannaccone ST, Krueger JM, Parsons JA, Shieh PB, Kavanagh S, Tauscher-Wisniewski S, McGill BE, Macek TA. Strauss KA, et al. Among authors: kwon jm. Nat Med. 2022 Jul;28(7):1381-1389. doi: 10.1038/s41591-022-01866-4. Epub 2022 Jun 17. Nat Med. 2022. PMID: 35715566 Free PMC article. Clinical Trial.
Artificial intelligence applied to electrocardiogram to rule out acute myocardial infarction: the ROMIAE multicentre study.
Lee MS, Shin TG, Lee Y, Kim DH, Choi SH, Cho H, Lee MJ, Jeong KY, Kim WY, Min YG, Han C, Yoon JC, Jung E, Kim WJ, Ahn C, Seo JY, Lim TH, Kim JS, Choi J, Kwon JM, Kim K; ROMIAE study group. Lee MS, et al. Among authors: kwon jm. Eur Heart J. 2025 May 21;46(20):1917-1929. doi: 10.1093/eurheartj/ehaf004. Eur Heart J. 2025. PMID: 39992309 Free PMC article.
Testing for Inborn Errors of Metabolism.
Kwon JM. Kwon JM. Continuum (Minneap Minn). 2018 Feb;24(1, Child Neurology):37-56. doi: 10.1212/CON.0000000000000563. Continuum (Minneap Minn). 2018. PMID: 29432236 Review.
The candidate gene approach.
Kwon JM, Goate AM. Kwon JM, et al. Alcohol Res Health. 2000;24(3):164-8. Alcohol Res Health. 2000. PMID: 11199286 Free PMC article. Review.
187 results