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Year Number of Results
1983 1
1986 1
1988 1
1990 2
1992 3
1993 2
1996 1
2000 2
2003 1
2005 1
2007 2
2008 1
2009 1
2010 1
2013 1
2014 5
2015 2
2016 1
2017 4
2018 3
2019 1
2020 3
2021 2
2022 2
2024 2
2025 0

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38 results

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Page 1
Dystrophinopathies.
Darras BT, Urion DK, Ghosh PS. Darras BT, et al. Among authors: urion dk. 2000 Sep 5 [updated 2022 Jan 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2000 Sep 5 [updated 2022 Jan 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301298 Free Books & Documents. Review.
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: urion dk. 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.
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay.
Tan S, Zhang Q, Zhan R, Luo S, Han Y, Yu B, Muss C, Pingault V, Marlin S, Delahaye A, Peters S, Perne C, Kreiß M, Spataro N, Trujillo-Quintero JP, Racine C, Tran-Mau-Them F, Phornphutkul C, Besterman AD, Martinez J, Wang X, Tian X, Srivastava S, Urion DK, Madden JA, Saif HA, Morrow MM, Begtrup A, Li X, Jurgensmeyer S, Leahy P, Zhou S, Li F, Hu Z, Tan J, Xia K, Guo H. Tan S, et al. Among authors: urion dk. Mol Psychiatry. 2024 Oct 29. doi: 10.1038/s41380-024-02806-z. Online ahead of print. Mol Psychiatry. 2024. PMID: 39472663
Neurologic Evaluation in Children With Laryngeal Cleft.
Walker RD, Irace AL, Kenna MA, Urion DK, Rahbar R. Walker RD, et al. Among authors: urion dk. JAMA Otolaryngol Head Neck Surg. 2017 Jul 1;143(7):651-655. doi: 10.1001/jamaoto.2016.4735. JAMA Otolaryngol Head Neck Surg. 2017. PMID: 28384788 Free PMC article.
Developing a New Set of ACGME Milestones for Child Neurology Residency.
Albert DVF, Bass N, Bodensteiner J, Draconi C, Duke ES, Felker M, Gropman A, Lotze T, Mink JW, Reese JJ Jr, Spiciarich M, Urion DK, Edgar L. Albert DVF, et al. Among authors: urion dk. Pediatr Neurol. 2021 Jan;114:47-52. doi: 10.1016/j.pediatrneurol.2020.10.008. Epub 2020 Oct 24. Pediatr Neurol. 2021. PMID: 33212335
Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective.
Dy ME, Waugh JL, Sharma N, O'Leary H, Kapur K, D'Gama AM, Sahin M, Urion DK, Kaufmann WE. Dy ME, et al. Among authors: urion dk. Pediatr Neurol. 2017 Oct;75:91-95. doi: 10.1016/j.pediatrneurol.2017.05.025. Epub 2017 Jun 2. Pediatr Neurol. 2017. PMID: 28838622 Free PMC article. Clinical Trial.
38 results