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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 1
2011 4
2012 3
2013 7
2014 7
2015 6
2016 5
2017 4
2018 1
2019 3
2020 5
2021 8
2022 1
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46 results
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Page 1
Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease.
Kim J, Hu C, Moufawad El Achkar C, Black LE, Douville J, Larson A, Pendergast MK, Goldkind SF, Lee EA, Kuniholm A, Soucy A, Vaze J, Belur NR, Fredriksen K, Stojkovska I, Tsytsykova A, Armant M, DiDonato RL, Choi J, Cornelissen L, Pereira LM, Augustine EF, Genetti CA, Dies K, Barton B, Williams L, Goodlett BD, Riley BL, Pasternak A, Berry ER, Pflock KA, Chu S, Reed C, Tyndall K, Agrawal PB, Beggs AH, Grant PE, Urion DK, Snyder RO, Waisbren SE, Poduri A, Park PJ, Patterson A, Biffi A, Mazzulli JR, Bodamer O, Berde CB, Yu TW. Kim J, et al. Among authors: augustine ef. N Engl J Med. 2019 Oct 24;381(17):1644-1652. doi: 10.1056/NEJMoa1813279. Epub 2019 Oct 9. N Engl J Med. 2019. PMID: 31597037 Free PMC article.
Deep Phenotyping of Parkinson's Disease.
Dorsey ER, Omberg L, Waddell E, Adams JL, Adams R, Ali MR, Amodeo K, Arky A, Augustine EF, Dinesh K, Hoque ME, Glidden AM, Jensen-Roberts S, Kabelac Z, Katabi D, Kieburtz K, Kinel DR, Little MA, Lizarraga KJ, Myers T, Riggare S, Rosero SZ, Saria S, Schifitto G, Schneider RB, Sharma G, Shoulson I, Stevenson EA, Tarolli CG, Luo J, McDermott MP. Dorsey ER, et al. Among authors: augustine ef. J Parkinsons Dis. 2020;10(3):855-873. doi: 10.3233/JPD-202006. J Parkinsons Dis. 2020. PMID: 32444562 Free PMC article. Review.
Batten disease: an expert update on agents in preclinical and clinical trials.
Masten MC, Mink JW, Augustine EF. Masten MC, et al. Among authors: augustine ef. Expert Opin Investig Drugs. 2020 Dec;29(12):1317-1322. doi: 10.1080/13543784.2020.1837110. Epub 2020 Nov 1. Expert Opin Investig Drugs. 2020. PMID: 33135495 Free PMC article. No abstract available.
Anxiety Symptoms Differ in Youth With and Without Tic Disorders.
Vermilion J, Pedraza C, Augustine EF, Adams HR, Vierhile A, Lewin AB, Collins AT, McDermott MP, O'Connor T, Kurlan R, van Wijngaarden E, Murphy TK, Mink JW. Vermilion J, et al. Among authors: augustine ef. Child Psychiatry Hum Dev. 2021 Apr;52(2):301-310. doi: 10.1007/s10578-020-01012-6. Child Psychiatry Hum Dev. 2021. PMID: 32519083
Challenges of Phenotype-Genotype Correlations in Rare Diseases.
Masten MC, Augustine EF, Mink JW. Masten MC, et al. Among authors: augustine ef. JAMA Ophthalmol. 2021 Dec 1;139(12):1323. doi: 10.1001/jamaophthalmol.2021.4372. JAMA Ophthalmol. 2021. PMID: 34709366 No abstract available.
A diagnostic confidence scheme for CLN3 disease.
Masten MC, Corre C, Paciorkowski AR, Vierhile A, Adams HR, Vermilion J, Zimmerman GA, Augustine EF, Mink JW. Masten MC, et al. Among authors: augustine ef. J Inherit Metab Dis. 2021 Nov;44(6):1453-1462. doi: 10.1002/jimd.12429. Epub 2021 Sep 7. J Inherit Metab Dis. 2021. PMID: 34453334
46 results