Veerapandiyan A - Search Results

1

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. 2025 Jan;31(1):332-341. doi: 10.1038/s41591-024-03304-z. Epub 2024 Oct 9. Nat Med. 2025. PMID: 39385046 Free PMC article. Clinical Trial.

2

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.

3

Pseudometabolic presentation of dystrophinopathy due to a missense mutation.

Veerapandiyan A, Shashi V, Jiang YH, Gallentine WB, Schoch K, Smith EC. Veerapandiyan A, et al. Muscle Nerve. 2010 Dec;42(6):975-9. doi: 10.1002/mus.21823. Muscle Nerve. 2010. PMID: 21104870 Free PMC article.

4

Use of Head Computed Tomography (CT) in the Pediatric Emergency Department in Evaluation of Children With New-Onset Afebrile Seizure.

Veerapandiyan A, Aravindhan A, Takahashi JH, Segal D, Pecor K, Ming X. Veerapandiyan A, et al. J Child Neurol. 2018 Oct;33(11):708-712. doi: 10.1177/0883073818786086. Epub 2018 Jul 10. J Child Neurol. 2018. PMID: 29987971

5

Two patients with an anti-N-methyl-D-aspartate receptor antibody syndrome-like presentation and negative results of testing for autoantibodies.

Shah R, Veerapandiyan A, Winchester S, Gallentine W, Mikati MA. Shah R, et al. Among authors: veerapandiyan a. Pediatr Neurol. 2011 Dec;45(6):412-6. doi: 10.1016/j.pediatrneurol.2011.09.012. Pediatr Neurol. 2011. PMID: 22115008

6

Structural connectivity of the frontal lobe in children with drug-resistant partial epilepsy.

Holt RL, Provenzale JM, Veerapandiyan A, Moon WJ, De Bellis MD, Leonard S, Gallentine WB, Grant GA, Egger H, Song AW, Mikati MA. Holt RL, et al. Among authors: veerapandiyan a. Epilepsy Behav. 2011 May;21(1):65-70. doi: 10.1016/j.yebeh.2011.03.016. Epub 2011 Apr 15. Epilepsy Behav. 2011. PMID: 21497558 Free PMC article.

7

Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study.

Shashi V, Veerapandiyan A, Keshavan MS, Zapadka M, Schoch K, Kwapil TR, Hooper SR, Stanley JA. Shashi V, et al. Among authors: veerapandiyan a. Biol Psychiatry. 2012 Oct 15;72(8):684-91. doi: 10.1016/j.biopsych.2012.04.023. Epub 2012 May 25. Biol Psychiatry. 2012. PMID: 22633947 Free PMC article.

8

Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation.

Deeb R, Veerapandiyan A, Tawil R, Treidler S. Deeb R, et al. Among authors: veerapandiyan a. Neurol Genet. 2018 Oct 25;4(6):e284. doi: 10.1212/NXG.0000000000000284. eCollection 2018 Dec. Neurol Genet. 2018. PMID: 30533530 Free PMC article. No abstract available.

9

Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.

Veerapandiyan A, Abdul-Rahman OA, Adam MP, Lyons MJ, Manning M, Coleman K, Kobrynski L, Taneja D, Schoch K, Zimmerman HH, Shashi V. Veerapandiyan A, et al. Am J Med Genet A. 2011 Sep;155A(9):2186-95. doi: 10.1002/ajmg.a.34226. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834039

10

A Rare Syndrome of GRID2 Deletion in 2 Siblings.

Veerapandiyan A, Enner S, Thulasi V, Ming X. Veerapandiyan A, et al. Child Neurol Open. 2017 Aug 22;4:2329048X17726168. doi: 10.1177/2329048X17726168. eCollection 2017 Jan-Dec. Child Neurol Open. 2017. PMID: 28856174 Free PMC article.

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