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

Yoshiaki Furukawa

Movement Disorders Research Laboratory

Centre for Addiction and Mental Health

The Clarke Division

Toronto

Canada

[email]@camh.net

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Movement Disorders Research Laboratory, Centre for Addiction and Mental Health, The Clarke Division, Toronto, Canada. 2000 - 2004
  • Movement Disorders Research Laboratory, Toronto Western Hospital, Ontario, Canada. 2000

References

  1. Amantadine for levodopa-induced choreic dyskinesia in compound heterozygotes for GCH1 mutations. Furukawa, Y., Filiano, J.J., Kish, S.J. Mov. Disord. (2004) [Pubmed]
  2. Serum prolactin in symptomatic and asymptomatic dopa-responsive dystonia due to a GCH1 mutation. Furukawa, Y., Guttman, M., Wong, H., Farrell, S.A., Furtado, S., Kish, S.J. Neurology (2003) [Pubmed]
  3. Brain proteasomal function in sporadic Parkinson's disease and related disorders. Furukawa, Y., Vigouroux, S., Wong, H., Guttman, M., Rajput, A.H., Ang, L., Briand, M., Kish, S.J., Briand, Y. Ann. Neurol. (2002) [Pubmed]
  4. Brain biopterin and tyrosine hydroxylase in asymptomatic dopa-responsive dystonia. Furukawa, Y., Kapatos, G., Haycock, J.W., Worsley, J., Wong, H., Kish, S.J., Nygaard, T.G. Ann. Neurol. (2002) [Pubmed]
  5. Dopa-responsive dystonia simulating spastic paraplegia due to tyrosine hydroxylase (TH) gene mutations. Furukawa, Y., Graf, W.D., Wong, H., Shimadzu, M., Kish, S.J. Neurology (2001) [Pubmed]
  6. Striatal dopamine in early-onset primary torsion dystonia with the DYT1 mutation. Furukawa, Y., Hornykiewicz, O., Fahn, S., Kish, S.J. Neurology (2000) [Pubmed]
  7. Scoliosis in a dopa-responsive dystonia family with a mutation of the GTP cyclohydrolase I gene. Furukawa, Y., Kish, S.J., Lang, A.E. Neurology (2000) [Pubmed]
 
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