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Aravindhan Veerapandiyan

TitleAssociate Professor
InstitutionUniversity of Arkansas for Medical Sciences
DepartmentPeds Pediatrics, College of Medicine
DivisionPeds Neurology
Address1900 Maryland Street
Mail Slot # 512-15
Little Rock AR 72202
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    Collapse Research 
    Collapse research activities and funding
    GR039105     (VEERAPANDIYAN, ARAVINDHAN)Jun 1, 2021 - Jun 30, 2023
    UAMS ACHRI Flow Through
    Clinical Neurobehavioral Screening Tool for Duchenne and Becker Muscular Dystrophy
    Role: Principal Investigator
    GR034028     (VEERAPANDIYAN, ARAVINDHAN)Feb 12, 2020 - Aug 31, 2020
    UAMS ACHRI Flow Through
    No FP attached
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions. Don't see publications published under other names? Login to add alternative names.
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    1. Wald ER, Eickhoff J, Flood GE, Heinz MV, Liu D, Agrawal A, Morse RP, Raney VM, Veerapandiyan A, Madan JC. Estimate of the incidence of PANDAS and PANS in 3 primary care populations. Front Pediatr. 2023; 11:1170379. PMID: 37808558.
      View in: PubMed
    2. Schuberth K, Ramani PK, Beemarajan E, Veerapandiyan A. Child Neurology: KMT2B-Related Dystonia in a Young Child With Worsening Gait Abnormality. Neurology. 2023 08 15; 101(7):328-332. PMID: 37041082.
      View in: PubMed
    3. Ramani PK, Fawcett K, Guntrum D, Samuel H, Ciafaloni E, Veerapandiyan A. Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies. Child Neurol Open. 2023 Jan-Dec; 10:2329048X231159484. PMID: 36844469.
      View in: PubMed
    4. Bryant G, Moore SA, Nix JS, Rice G, Gokden M, Veerapandiyan A. Miyoshi Muscular Dystrophy Due to Novel Splice Site Variants in DYSF Gene. Child Neurol Open. 2022 Jan-Dec; 9:2329048X221140298. PMID: 36419651.
      View in: PubMed
    5. ElSheikh RH, Aravindhan A, Boysen S, Veerapandiyan A. Infantile-Onset Complex Hereditary Spastic Paraplegia Due to a Novel Mutation in SPAST Gene. Pediatr Neurol. 2022 09; 134:71. PMID: 35841713.
      View in: PubMed
    6. 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. An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy. Ann Clin Transl Neurol. 2022 06; 9(6):810-818. PMID: 35567422.
      View in: PubMed
    7. Willis E, Moore SA, Cox MO, Stefans V, Aravindhan A, Gokden M, Veerapandiyan A. Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in FKRP Gene. Child Neurol Open. 2022 Jan-Dec; 9:2329048X221097518. PMID: 35557983.
      View in: PubMed
    8. Veerapandiyan A, Rao VK. Palliative care in Duchenne muscular dystrophy: Goals of care discussions and beyond. Muscle Nerve. 2022 06; 65(6):627-629. PMID: 35362613.
      View in: PubMed
    9. Boysen S, Elumalai V, ElSheikh RH, Aravindhan A, Veerapandiyan A. Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene. J Clin Neurosci. 2022 06; 100:212-213. PMID: 35181192.
      View in: PubMed
    10. Sharma R, Aravindhan A, Puente C, Veerapandiyan A. Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay due to Novel Mutations in the SACS Gene. J Investig Med High Impact Case Rep. 2022 Jan-Dec; 10:23247096221139670. PMID: 36458808.
      View in: PubMed
    11. Rubenstein S, Grew E, Clouser K, Kwok A, Veerapandiyan A, Kornitzer J, Pecor K, Ming X. COVID-19 in Pediatric Inpatients: A Multi-Center Observational Study of Factors Associated with Negative Short-Term Outcomes. Children (Basel). 2021 Oct 22; 8(11). PMID: 34828664.
      View in: PubMed
    12. Steele JL, Morrow MM, Sarnat HB, Alkhunaizi E, Brandt T, Chitayat DA, DeFilippo CP, Douglas GV, Dubbs HA, Elloumi HZ, Glassford MR, Hannibal MC, H?ron 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. Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome. Pediatr Neurol. 2022 01; 126:65-73. PMID: 34740135.
      View in: PubMed
    13. Dhasakeerthi T, Aravindhan A, Woodall A, Mills W, Veerapandiyan A. Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene. J Clin Neuromuscul Dis. 2021 Sep 01; 23(1):54-55. PMID: 34431804.
      View in: PubMed
    14. Gill PS, Clothier JL, Veerapandiyan A, Dweep H, Porter-Gill PA, Schaefer GB. Molecular Dysregulation in Autism Spectrum Disorder. J Pers Med. 2021 Aug 27; 11(9). PMID: 34575625.
      View in: PubMed
    15. Samanta D, Veerapandiyan A, Burrow TA, Gokden M. Mitochondrial Ultrastructural Defects in NDUFS3-Related Disorder. J Pediatr Neurosci. 2021 Oct-Dec; 16(4):299-302. PMID: 36531773.
      View in: PubMed
    16. Gill PS, Yu FB, Porter-Gill PA, Boyanton BL, Allen JC, Farrar JE, Veerapandiyan A, Prodhan P, Bielamowicz KJ, Sellars E, Burrow A, Kennedy JL, Clothier JL, Becton DL, Rule D, Schaefer GB. Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children's Hospital. J Pers Med. 2021 May 11; 11(5). PMID: 34064668.
      View in: PubMed
    17. Weerasinghe D, Veerapandiyan A, Stanton M, Herrmann DN, Akmyradov C, Logigian E. Recovery of foot drop in chronic inflammatory demyelinating polyneuropathy (CIDP). Muscle Nerve. 2021 07; 64(1):59-63. PMID: 33876440.
      View in: PubMed
    18. Lewis HS, Srinivasa Sekaran BS, Stefans V, Veerapandiyan A. Clinical Reasoning: A 6-Year-Old Boy With Muscle Twitching. Neurology. 2021 01 12; 96(2):e301-e304. PMID: 32917800.
      View in: PubMed
    19. Harada Y, Rao VK, Arya K, Kuntz NL, DiDonato CJ, Napchan-Pomerantz G, Agarwal A, Stefans V, Katsuno M, Veerapandiyan A. Combination molecular therapies for type 1 spinal muscular atrophy. Muscle Nerve. 2020 10; 62(4):550-554. PMID: 32710634.
      View in: PubMed
    20. Ranabothu S, Onteddu S, Nalleballe K, Dandu V, Veerapaneni K, Veerapandiyan A. Spectrum of COVID-19 in children. Acta Paediatr. 2020 09; 109(9):1899-1900. PMID: 32538518.
      View in: PubMed
    21. Saylam E, Aravindhan A, Stefans V, Veerapandiyan A. Pseudometabolic Presentation of Dystrophinopathy in a Family Due to a Rare Nonsense Mutation. J Clin Neuromuscul Dis. 2020 Jun; 21(4):245-246. PMID: 32453103.
      View in: PubMed
    22. Malatesta L, Arya K, Gokden M, Stefans V, Veerapandiyan A. BAG3 Myopathy Presenting With Prominent Neuropathic Phenotype and No Cardiac or Respiratory Involvement: A Case Report and Literature Review. J Clin Neuromuscul Dis. 2020 Jun; 21(4):230-239. PMID: 32453099.
      View in: PubMed
    23. Feldman AG, Parsons JA, Dutmer CM, Veerapandiyan A, Hafberg E, Maloney N, Mack CL. Subacute Liver Failure Following Gene Replacement Therapy for Spinal Muscular Atrophy Type 1. J Pediatr. 2020 10; 225:252-258.e1. PMID: 32473148.
      View in: PubMed
    24. Veerapandiyan A, Wagner KR, Apkon S, McDonald CM, Mathews KD, Parsons JA, Wong BL, Eichinger K, Shieh PB, Butterfield RJ, Rao VK, Smith EC, Proud CM, Connolly AM, Ciafaloni E. The care of patients with Duchenne, Becker, and other muscular dystrophies in the COVID-19 pandemic. Muscle Nerve. 2020 07; 62(1):41-45. PMID: 32329920.
      View in: PubMed
    25. 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. Spinal muscular atrophy care in the COVID-19 pandemic era. Muscle Nerve. 2020 07; 62(1):46-49. PMID: 32329921.
      View in: PubMed
    26. Harada Y, Zuchner SL, Herrmann DN, Veerapandiyan A. Clinical Reasoning: A case of bilateral foot drop in a 74-year-old man. Neurology. 2020 03 03; 94(9):405-409. PMID: 32041727.
      View in: PubMed
    27. Guess KE, Harada Y, Hill A, Ferry J, Veerapandiyan A. A Toddler With Bilateral Facial Weakness. Clin Pediatr (Phila). 2020 05; 59(4-5):529-531. PMID: 31948285.
      View in: PubMed
    28. Saylam E, Moore SA, Aravindhan A, Marton H, Nagy PL, Gokden M, Cox MO, Stefans V, Veerapandiyan A. A novel noncoding FKRP mutation in early onset limb-girdle muscular dystrophy. Neurol Genet. 2020 Feb; 6(1):e388. PMID: 32042916.
      View in: PubMed
    29. Veerapandiyan A, Eichinger K, Guntrum D, Kwon J, Baker L, Collins E, Ciafaloni E. Nusinersen for older patients with spinal muscular atrophy: A real-world clinical setting experience. Muscle Nerve. 2020 02; 61(2):222-226. PMID: 31773738.
      View in: PubMed
    30. Lewis HS, Willis E, Veerapandiyan A. Charcot-Marie-Tooth Disease Type 4J and Multiple Sclerosis. J Clin Neuromuscul Dis. 2019 Dec; 21(2):117-118. PMID: 31743256.
      View in: PubMed
    31. Mulvey MA, Veerapandiyan A, Marks DA, Ming X. Electronic health record cue identifies epilepsy patients at risk for obstructive sleep apnea. Neurol Clin Pract. 2018 Dec; 8(6):468-471. PMID: 30588375.
      View in: PubMed
    32. Deeb R, Veerapandiyan A, Tawil R, Treidler S. Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation. Neurol Genet. 2018 Dec; 4(6):e284. PMID: 30533530.
      View in: PubMed
    33. Silverstein S, Veerapandiyan A, Hayes-Rosen C, Ming X, Kornitzer J. A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia. Metab Brain Dis. 2019 02; 34(1):373-376. PMID: 30350008.
      View in: PubMed
    34. Veerapandiyan A, Oh D, Kornitzer J. Distal 1q21.1 and proximal 1q21.2 microduplication in a child with attention-deficit hyperactivity disorder. Acta Neurol Belg. 2019 Jun; 119(2):289-290. PMID: 30120686.
      View in: PubMed
    35. Veerapandiyan A, Pal R, D'Ambrosio S, Young I, Eichinger K, Collins E, Westesson PL, Kwon J, Ciafaloni E. Cervical puncture to deliver nusinersen in patients with spinal muscular atrophy. Neurology. 2018 08 14; 91(7):e620-e624. PMID: 30006410.
      View in: PubMed
    36. Veerapandiyan A, Aravindhan A, Takahashi JH, Segal D, Pecor K, Ming X. Use of Head Computed Tomography (CT) in the Pediatric Emergency Department in Evaluation of Children With New-Onset Afebrile Seizure. J Child Neurol. 2018 10; 33(11):708-712. PMID: 29987971.
      View in: PubMed
    37. Aravindhan A, Shah K, Pak J, Veerapandiyan A. Early-onset epileptic encephalopathy with myoclonic seizures related to 9q33.3-q34.11 deletion involving STXBP1 and SPTAN1 genes. Epileptic Disord. 2018 Jun 01; 20(3):214-218. PMID: 29897043.
      View in: PubMed
    38. Aravindhan A, Veerapandiyan A, Earley C, Thulasi V, Kresge C, Kornitzer J. Child Neurology: Type 1 sialidosis due to a novel mutation in NEU1 gene. Neurology. 2018 03 27; 90(13):622-624. PMID: 29581327.
      View in: PubMed
    39. Veerapandiyan A, Enner S, Thulasi V, Ming X. A Rare Syndrome of GRID2 Deletion in 2 Siblings. Child Neurol Open. 2017 Jan-Dec; 4:2329048X17726168. PMID: 28856174.
      View in: PubMed
    40. Thulasi V, Veerapandiyan A, Pletcher BA, Tong CM, Ming X. A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin. Child Neurol Open. 2017 Jan-Dec; 4:2329048X17725610. PMID: 28856173.
      View in: PubMed
    41. Veerapandiyan A, Chaudhari A, Deo P, Ming X. Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS): A pediatric case report with six year follow-up. Mult Scler Relat Disord. 2017 Oct; 17:95-98. PMID: 29055484.
      View in: PubMed
    42. Veerapandiyan A, Chaudhari A, Traba CM, Ming X. Novel mutation in mitochondrial DNA in 2 siblings with Leigh syndrome. Neurol Genet. 2016 Oct; 2(5):e99. PMID: 27574709.
      View in: PubMed
    43. Leonard AS, Hyder SN, Kolls BJ, Arehart E, Ng KC, Veerapandiyan A, Mikati MA. Seizure predisposition after perinatal hypoxia: effects of subsequent age and of an epilepsy predisposing gene mutation. Epilepsia. 2013 Oct; 54(10):1789-800. PMID: 24032507.
      View in: PubMed
    44. Steele SU, Cheah SM, Veerapandiyan A, Gallentine W, Smith EC, Mikati MA. Electroencephalographic and seizure manifestations in two patients with folate receptor autoimmune antibody-mediated primary cerebral folate deficiency. Epilepsy Behav. 2012 Aug; 24(4):507-12. PMID: 22749608.
      View in: PubMed
    45. Shashi V, Veerapandiyan A, Keshavan MS, Zapadka M, Schoch K, Kwapil TR, Hooper SR, Stanley JA. Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study. Biol Psychiatry. 2012 Oct 15; 72(8):684-91. PMID: 22633947.
      View in: PubMed
    46. Veerapandiyan A, Singh P, Mikati MA. Possible induction of West syndrome by oxcarbazepine therapy in a patient with complex partial seizures. Epileptic Disord. 2012 Mar; 14(1):99-103. PMID: 22425652.
      View in: PubMed
    47. Shah R, Veerapandiyan A, Winchester S, Gallentine W, Mikati MA. Two patients with an anti-N-methyl-D-aspartate receptor antibody syndrome-like presentation and negative results of testing for autoantibodies. Pediatr Neurol. 2011 Dec; 45(6):412-6. PMID: 22115008.
      View in: PubMed
    48. Shashi V, Veerapandiyan A, Schoch K, Kwapil T, Keshavan M, Ip E, Hooper S. Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions. J Intellect Disabil Res. 2012 Sep; 56(9):865-78. PMID: 21883601.
      View in: PubMed
    49. Veerapandiyan A, Abdul-Rahman OA, Adam MP, Lyons MJ, Manning M, Coleman K, Kobrynski L, Taneja D, Schoch K, Zimmerman HH, Shashi V. Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge. Am J Med Genet A. 2011 Sep; 155A(9):2186-95. PMID: 21834039.
      View in: PubMed
    50. Holt RL, Provenzale JM, Veerapandiyan A, Moon WJ, De Bellis MD, Leonard S, Gallentine WB, Grant GA, Egger H, Song AW, Mikati MA. Structural connectivity of the frontal lobe in children with drug-resistant partial epilepsy. Epilepsy Behav. 2011 May; 21(1):65-70. PMID: 21497558.
      View in: PubMed
    51. Veerapandiyan A, Gallentine WB, Winchester SA, Baker J, Kansagra SM, Mikati MA. Oculogyric crises secondary to lamotrigine overdosage. Epilepsia. 2011 Mar; 52(3):e4-6. PMID: 21395567.
      View in: PubMed
    52. Veerapandiyan A, Blalock D, Ghosh S, Ip E, Barnes C, Shashi V. The role of cephalometry in assessing velopharyngeal dysfunction in velocardiofacial syndrome. Laryngoscope. 2011 Apr; 121(4):732-7. PMID: 21305558.
      View in: PubMed
    53. Veerapandiyan A, Winchester SA, Gallentine WB, Smith EC, Kansagra S, Hyland K, Mikati MA. Electroencephalographic and seizure manifestations of pyridoxal 5'-phosphate-dependent epilepsy. Epilepsy Behav. 2011 Mar; 20(3):494-501. PMID: 21292558.
      View in: PubMed
    54. Veerapandiyan A, Shashi V, Jiang YH, Gallentine WB, Schoch K, Smith EC. Pseudometabolic presentation of dystrophinopathy due to a missense mutation. Muscle Nerve. 2010 Dec; 42(6):975-9. PMID: 21104870.
      View in: PubMed
    55. Veerapandiyan A, Chinn IK, Schoch K, Maloney KA, Shashi V. Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation. Eur J Med Genet. 2011 Jan-Feb; 54(1):63-6. PMID: 20887823.
      View in: PubMed
    56. Goldstein JL, Austin SL, Boyette K, Kanaly A, Veerapandiyan A, Rehder C, Kishnani PS, Bali DS. Molecular analysis of the AGL gene: identification of 25 novel mutations and evidence of genetic heterogeneity in patients with Glycogen Storage Disease Type III. Genet Med. 2010 Jul; 12(7):424-30. PMID: 20648714.
      View in: PubMed
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