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Connection

Aravindhan Veerapandiyan to Adult

This is a "connection" page, showing publications Aravindhan Veerapandiyan has written about Adult.

 
Connection Strength
 
 
 
0.183
 
  1. 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.
    View in: PubMed
    Score: 0.058
  2. 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.
    View in: PubMed
    Score: 0.032
  3. 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.
    View in: PubMed
    Score: 0.031
  4. 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.
    View in: PubMed
    Score: 0.017
  5. 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.
    View in: PubMed
    Score: 0.016
  6. 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.
    View in: PubMed
    Score: 0.016
  7. 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.
    View in: PubMed
    Score: 0.013
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.