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This is a "connection" page, showing publications co-authored by Murat Gokden and Aravindhan Veerapandiyan.

Connection Strength
  1. 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.
    View in: PubMed
    Score: 0.233
  2. 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.
    View in: PubMed
    Score: 0.224
  3. 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.
    View in: PubMed
    Score: 0.212
  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.
    View in: PubMed
    Score: 0.196
  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.
    View in: PubMed
    Score: 0.190
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.