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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.
Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies.
Ramani PK, Fawcett K, Guntrum D, Samuel H, Ciafaloni E, Veerapandiyan A. Ramani PK, et al. Among authors: veerapandiyan a. Child Neurol Open. 2023 Feb 22;10:2329048X231159484. doi: 10.1177/2329048X231159484. eCollection 2023 Jan-Dec. Child Neurol Open. 2023. PMID: 36844469 Free PMC article.
Charcot-Marie-Tooth Disease Type 4J and Multiple Sclerosis.
Lewis HS, Willis E, Veerapandiyan A. Lewis HS, et al. Among authors: veerapandiyan a. J Clin Neuromuscul Dis. 2019 Dec;21(2):117-118. doi: 10.1097/CND.0000000000000258. J Clin Neuromuscul Dis. 2019. PMID: 31743256 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.
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.
59 results