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

Year Number of Results
1993 1
2004 1
2010 3
2011 8
2012 4
2013 1
2016 1
2017 3
2018 9
2019 5
2020 12
2021 7
2022 6
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51 results
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Page 1
Andersen-Tawil Syndrome.
Veerapandiyan A, Statland JM, Tawil R. Veerapandiyan A, et al. 2004 Nov 22 [updated 2018 Jun 7]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2004 Nov 22 [updated 2018 Jun 7]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301441 Free Books & Documents. Review.
Molecular Dysregulation in Autism Spectrum Disorder.
Gill PS, Clothier JL, Veerapandiyan A, Dweep H, Porter-Gill PA, Schaefer GB. Gill PS, et al. Among authors: veerapandiyan a. J Pers Med. 2021 Aug 27;11(9):848. doi: 10.3390/jpm11090848. J Pers Med. 2021. PMID: 34575625 Free PMC article. Review.
Spectrum of COVID-19 in children.
Ranabothu S, Onteddu S, Nalleballe K, Dandu V, Veerapaneni K, Veerapandiyan A. Ranabothu S, et al. Among authors: veerapandiyan a. Acta Paediatr. 2020 Sep;109(9):1899-1900. doi: 10.1111/apa.15412. Epub 2020 Jul 30. Acta Paediatr. 2020. PMID: 32538518 Free PMC article. No abstract available.
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.
Clinical Reasoning: A 6-Year-Old Boy With Muscle Twitching.
Lewis HS, Srinivasa Sekaran BS, Stefans V, Veerapandiyan A. Lewis HS, et al. Among authors: veerapandiyan a. Neurology. 2021 Jan 12;96(2):e301-e304. doi: 10.1212/WNL.0000000000010746. Epub 2020 Sep 11. Neurology. 2021. PMID: 32917800 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.
Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene.
Dhasakeerthi T, Aravindhan A, Woodall A, Mills W, Veerapandiyan A. Dhasakeerthi T, et al. Among authors: veerapandiyan a. J Clin Neuromuscul Dis. 2021 Sep 1;23(1):54-55. doi: 10.1097/CND.0000000000000336. J Clin Neuromuscul Dis. 2021. PMID: 34431804 No abstract available.
51 results