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Year | Number of Results |
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2016 | 2 |
2017 | 3 |
2018 | 2 |
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2024 | 0 |
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Page 1
Venous Thromboembolism in Prader-Willi Syndrome: A Questionnaire Survey.
Genes (Basel). 2019 Jul 19;10(7):550. doi: 10.3390/genes10070550.
Genes (Basel). 2019.
PMID: 31331040
Free PMC article.
Survival trends from the Prader-Willi Syndrome Association (USA) 40-year mortality survey.
Manzardo AM, Loker J, Heinemann J, Loker C, Butler MG.
Manzardo AM, et al. Among authors: loker j.
Genet Med. 2018 Jan;20(1):24-30. doi: 10.1038/gim.2017.92. Epub 2017 Jul 6.
Genet Med. 2018.
PMID: 28682308
Free PMC article.
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Congenital aneurysm of both left ventricle and left atrium.
Halas RF, Schmehil CJ, Ten Eyck GR, Loker JL.
Halas RF, et al. Among authors: loker jl.
Ann Pediatr Cardiol. 2018 Jan-Apr;11(1):97-99. doi: 10.4103/apc.APC_55_17.
Ann Pediatr Cardiol. 2018.
PMID: 29440840
Free PMC article.
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Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey.
Butler MG, Manzardo AM, Heinemann J, Loker C, Loker J.
Butler MG, et al. Among authors: loker j.
Genet Med. 2017 Jun;19(6):635-642. doi: 10.1038/gim.2016.178. Epub 2016 Nov 17.
Genet Med. 2017.
PMID: 27854358
Free PMC article.
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Cardiac fibroma with cardiac arrest: a rare clinical presentation of Gorlin syndrome in an 8-month-old infant.
Baidoun M, Elgendy M, Loker J.
Baidoun M, et al. Among authors: loker j.
BMJ Case Rep. 2021 Jun 23;14(6):e241519. doi: 10.1136/bcr-2020-241519.
BMJ Case Rep. 2021.
PMID: 34162607
Free PMC article.
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Rare Diagnosis in a 4-Year-Old Boy Presenting With Shortness of Breath.
Schmehil CJ, Halas RF, Malhotra D, Loker J.
Schmehil CJ, et al. Among authors: loker j.
Clin Pediatr (Phila). 2017 Nov;56(13):1263-1265. doi: 10.1177/0009922816674525. Epub 2016 Oct 23.
Clin Pediatr (Phila). 2017.
PMID: 27798395
No abstract available.
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