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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Kevin J. Felice

Department of Neurology

University of Connecticut School of Medicine

Farmington 06030



Name/email consistency: high



  • Department of Neurology, University of Connecticut School of Medicine, Farmington 06030, USA. 1998 - 2005


  1. Facioscapulohumeral dystrophy presenting as infantile facial diplegia and late-onset limb-girdle myopathy in members of the same family. Felice, K.J., Jones, J.M., Conway, S.R. Muscle. Nerve (2005) [Pubmed]
  2. Postinfectious myasthenia gravis: report of two children. Felice, K.J., DiMario, F.J., Conway, S.R. J. Child Neurol. (2005) [Pubmed]
  3. Benign calf amyotrophy: clinicopathologic study of 8 patients. Felice, K.J., Whitaker, C.H., Grunnet, M.L. Arch. Neurol. (2003) [Pubmed]
  4. Monofocal motor neuropathy: Improvement with intravenous immunoglobulin. Felice, K.J., Goldstein, J.M. Muscle. Nerve (2002) [Pubmed]
  5. Unusual clinical presentations in patients harboring the facioscapulohumeral dystrophy 4q35 deletion. Felice, K.J., Moore, S.A. Muscle. Nerve (2001) [Pubmed]
  6. Inclusion body myositis in Connecticut: observations in 35 patients during an 8-year period. Felice, K.J., North, W.A. Medicine. (Baltimore) (2001) [Pubmed]
  7. Severe X-linked Charcot-Marie-Tooth neuropathy due to new mutations [G59R(G-->C), W44X(G-->A)] in the connexin 32 gene. Felice, K.J., Seltzer, W.K. Eur. Neurol. (2000) [Pubmed]
  8. Adult-onset MLD: a gene mutation with isolated polyneuropathy. Felice, K.J., Gomez Lira, M., Natowicz, M., Grunnet, M.L., Tsongalis, G.J., Sima, A.A., Kaplan, R.F. Neurology (2000) [Pubmed]
  9. Autosomal dominant distal myopathy not linked to the known distal myopathy loci. Felice, K.J., Meredith, C., Binz, N., Butler, A., Jacob, R., Akkari, P., Hallmayer, J., Laing, N. Neuromuscul. Disord. (1999) [Pubmed]
  10. Creatine kinase values in amyotrophic lateral sclerosis. Felice, K.J., North, W.A. J. Neurol. Sci. (1998) [Pubmed]
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