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A Toddler With Bilateral Facial Weakness.
Guess KE, Harada Y, Hill A, Ferry J, Veerapandiyan A. Guess KE, et al. Among authors: veerapandiyan a. Clin Pediatr (Phila). 2020 May;59(4-5):529-531. doi: 10.1177/0009922819901007. Epub 2020 Jan 16. Clin Pediatr (Phila). 2020. PMID: 31948285 No abstract available.
Spinal muscular atrophy care in the COVID-19 pandemic era.
Veerapandiyan A, Connolly AM, Finkel RS, Arya K, Mathews KD, Smith EC, Castro D, Butterfield RJ, Parsons JA, Servais L, Kuntz N, Rao VK, Brandsema JF, Mercuri E, Ciafaloni E. Veerapandiyan A, et al. Muscle Nerve. 2020 Jul;62(1):46-49. doi: 10.1002/mus.26903. Epub 2020 May 3. Muscle Nerve. 2020. PMID: 32329921 Free PMC article. Review.
Combination molecular therapies for type 1 spinal muscular atrophy.
Harada Y, Rao VK, Arya K, Kuntz NL, DiDonato CJ, Napchan-Pomerantz G, Agarwal A, Stefans V, Katsuno M, Veerapandiyan A. Harada Y, et al. Among authors: veerapandiyan a. Muscle Nerve. 2020 Oct;62(4):550-554. doi: 10.1002/mus.27034. Epub 2020 Aug 10. Muscle Nerve. 2020. PMID: 32710634
An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy.
Kwon JM, Arya K, Kuntz N, Phan HC, Sieburg C, Swoboda KJ, Veerapandiyan A, Assman B, Bader-Weder S, Dickendesher TL, Hansen J, Lin H, Yan Y, Rao VK; US Expanded Access Program Working Group. Kwon JM, et al. Among authors: veerapandiyan a. Ann Clin Transl Neurol. 2022 Jun;9(6):810-818. doi: 10.1002/acn3.51560. Epub 2022 May 14. Ann Clin Transl Neurol. 2022. PMID: 35567422 Free PMC article.
Miyoshi Muscular Dystrophy Due to Novel Splice Site Variants in DYSF Gene.
Bryant G, Moore SA, Nix JS, Rice G, Gokden M, Veerapandiyan A. Bryant G, et al. Among authors: veerapandiyan a. Child Neurol Open. 2022 Nov 16;9:2329048X221140298. doi: 10.1177/2329048X221140298. eCollection 2022 Jan-Dec. Child Neurol Open. 2022. PMID: 36419651 Free PMC article.
59 results