Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

68 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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.
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
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.
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.
Steele JL, Morrow MM, Sarnat HB, Alkhunaizi E, Brandt T, Chitayat DA, DeFilippo CP, Douglas GV, Dubbs HA, Elloumi HZ, Glassford MR, Hannibal MC, Héron B, Kim LE, Marco EJ, Mignot C, Monaghan KG, Myers KA, Parikh S, Quinonez SC, Rajabi F, Shankar SP, Shinawi MS, van de Kamp JJP, Veerapandiyan A, Waldman AT, Graf WD. Steele JL, et al. Among authors: veerapandiyan a. Pediatr Neurol. 2022 Jan;126:65-73. doi: 10.1016/j.pediatrneurol.2021.10.008. Epub 2021 Oct 18. Pediatr Neurol. 2022. PMID: 34740135 Free article.
AAV gene therapy for Duchenne muscular dystrophy: the EMBARK phase 3 randomized trial.
Mendell JR, Muntoni F, McDonald CM, Mercuri EM, Ciafaloni E, Komaki H, Leon-Astudillo C, Nascimento A, Proud C, Schara-Schmidt U, Veerapandiyan A, Zaidman CM, Guridi M, Murphy AP, Reid C, Wandel C, Asher DR, Darton E, Mason S, Potter RA, Singh T, Zhang W, Fontoura P, Elkins JS, Rodino-Klapac LR. Mendell JR, et al. Among authors: veerapandiyan a. Nat Med. 2024 Oct 9. doi: 10.1038/s41591-024-03304-z. Online ahead of print. Nat Med. 2024. PMID: 39385046
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.
68 results