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Vikki Stefans

TitleProfessor
InstitutionUniversity of Arkansas for Medical Sciences
DepartmentPeds Pediatrics, College of Medicine
DivisionPeds Developmental Peds
Address4028-1 ACH Administration
1900 Maryland Street
Mail Slot # 512-41
Little Rock AR 72202
Phone501-364-4374
ORCID ORCID Icon0000-0002-2939-7190 Additional info
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    Other Positions
    TitleProfessor
    InstitutionUniversity of Arkansas for Medical Sciences
    DepartmentPhysical Medicine and Rehabilitation, College of Medicine


    Collapse Research 
    Collapse research activities and funding
    492481     (KOVVURU, SUKANTHI)Jan 1, 2017 - Jun 30, 2025
    Muscular Dystrophy Association
    MDA Care Center Grant - Continuation
    Role: Co-Investigator

    Collapse Outreach 

    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. 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
    2. 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
    3. 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
    4. 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
    5. 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
    6. Zarate YA, Boccuto L, Srikanth S, Pauly R, Ocal E, Balmakund T, Hinkle K, Stefans V, Schaefer GB, Collins RT. Constitutive activation of the PI3K-AKT pathway and cardiovascular abnormalities in an individual with Kosaki overgrowth syndrome. Am J Med Genet A. 2019 06; 179(6):1047-1052. PMID: 30941910.
      View in: PubMed
    7. Sonderman KA, Wolf LL, Armstrong LB, Taylor K, Jiang W, Weil BR, Koehlmoos TP, Ricca RL, Weldon CB, Haider AH, Rice-Townsend SE. Testicular atrophy following inguinal hernia repair in children. Pediatr Surg Int. 2018 May; 34(5):553-560. PMID: 29735374.
      View in: PubMed
    8. Sonderman KA, Wolf LL, Armstrong LB, Taylor K, Jiang W, Weil BR, Koehlmoos TP, Ricca RL, Weldon CB, Haider AH, Rice-Townsend SE. Testicular atrophy following inguinal hernia repair in children. Pediatr Surg Int. 2018 May; 34(5):553-560. PMID: 30439755.
      View in: PubMed
    9. Sonderman KA, Wolf LL, Armstrong LB, Taylor K, Jiang W, Weil BR, Koehlmoos TP, Ricca RL, Weldon CB, Haider AH, Rice-Townsend SE. Testicular atrophy following inguinal hernia repair in children. Pediatr Surg Int. 2018 May; 34(5):553-560. PMID: 26310427.
      View in: PubMed
    10. Tanaka AJ, Cho MT, Willaert R, Retterer K, Zarate YA, Bosanko K, Stefans V, Oishi K, Williamson A, Wilson GN, Basinger A, Barbaro-Dieber T, Ortega L, Sorrentino S, Gabriel MK, Anderson IJ, Sacoto MJG, Schnur RE, Chung WK. De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism. Cold Spring Harb Mol Case Stud. 2017 Nov; 3(6). PMID: 29162653.
      View in: PubMed
    11. Stefans V, Tompkins, E, Walters, W. A confusing case with mixed findings. Journal of Clinical Neuromuscular Disease, March 2014 - Volume 15. 2014; 21-22.
    12. Stefans V. Omics and EBM: Towards the Art of Individualization or the Standardization of Science - Which Way is this Train Headed? (Editorial). Pediat Therapeut. 2012; 2(4):1-2.
    13. Buschbacher, Ralph MD, Editor, Kortebein, Patrick MD, Means, Kevin M MD. Rehabilitation Medicine Quick Reference: Geriatrics. Age-Related Changes: Bone and Evaluation of Osteoporosis: Detection of Significant Bone Loss. 2012; 2 and 24.
    14. McGoogan KE, Haafiz AB, Gonz?lez Peralta RP. Herpes simplex virus hepatitis in infants: clinical outcomes and correlates of disease severity. J Pediatr. 2011 Oct; 159(4):608-11. PMID: 2059124.
      View in: PubMed
    15. McGoogan KE, Haafiz AB, Gonz?lez Peralta RP. Herpes simplex virus hepatitis in infants: clinical outcomes and correlates of disease severity. J Pediatr. 2011 Oct; 159(4):608-11. PMID: 9305265.
      View in: PubMed
    16. McGoogan KE, Haafiz AB, Gonz?lez Peralta RP. Herpes simplex virus hepatitis in infants: clinical outcomes and correlates of disease severity. J Pediatr. 2011 Oct; 159(4):608-11. PMID: 32917800.
      View in: PubMed
    17. Aitken ME, Korehbandi P, Parnell D, Parker JG, Stefans V, Tompkins E, Schulz EG. Experiences from the development of a comprehensive family support program for pediatric trauma and rehabilitation patients. Arch Phys Med Rehabil. 2005 Jan; 86(1):175-9. PMID: 15641010.
      View in: PubMed
    18. Farley T, Vines C, McCluer S, Stefans V, Hunter J. Secondary disabilities in Arkansas with spina bifida. Eur J Pediatr Surg. 1994 Dec; 4 Suppl 1:39-40. PMID: 7766555.
      View in: PubMed
    19. Stefans V. Steps and Missteps in Genetic Diagnosis of a Rare Mitochondrial Myopathy.
    20. Stefans V, Tompkins, E, Walters, W. A confusing case with mixed findings. Spinal Muscular Atrophy and Chiari with UMN syndrome.
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