Skip to main content
SpringerLink
Log in

Pharmacological Probing of Type 1 Autism

  • Letter to the Editor
  • Published:
Journal of Autism and Developmental Disorders Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  • Alarcón, M., Abrahams, B. S., Stone, J. L., Duvall, J. A., Perederiy, J. V., Bomar, J. M., et al. (2008). Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. American Journal of Human Genetics, 82, 150–159. doi:10.1016/j.ajhg.2007.09.005.

    Article  PubMed  Google Scholar 

  • Arking, D. E., Cutler, D. J., Brune, C. W., Teslovich, T. M., West, K., Ikeda, M., et al. (2008). A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics, 82, 160–164. doi:10.1016/j.ajhg.2007.09.015.

    Article  PubMed  Google Scholar 

  • Bakkaloglu, B., O’Roak, B. J., Louvi, A., Gupta, A. R., Abelson, J. F., Morgan, T. M., et al. (2008). Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. American Journal of Human Genetics, 82, 165–173. doi:10.1016/j.ajhg.2007.09.017.

    Article  PubMed  Google Scholar 

  • Manev, R., & Manev, H. (2001). Aminoglycoside antibiotics and autism: a speculative hypothesis. BMC Psychiatry, 1, 5.

    Article  PubMed  Google Scholar 

  • Stephan, D. A. (2008). Unraveling autism. American Journal of Human Genetics, 82, 7–9. doi:10.1016/j.ajhg.2007.12.003.

    Article  PubMed  Google Scholar 

  • Strauss, K. A., Puffenberger, E. G., Huentelman, M. J., Gottlieb, S., Dobrin, S. E., Parod, J. M., et al. (2006). Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. The New England Journal of Medicine, 354, 1370–1377. doi:10.1056/NEJMoa052773.

    Article  PubMed  Google Scholar 

  • Welch, E. M., Barton, E. R., Zhuo, J., Tomizawa, Y., Friesen, W. J., Trifillis, P., et al. (2007). PTC124 targets genetic disorders caused by nonsense mutations. Nature, 447, 87–91.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Department of Psychiatry, The Psychiatric Institute, University of Illinois at Chicago, 1601 West Taylor Street, MC912, Chicago, IL, 60612, USA

    Hari Manev & Radmila Manev

Authors
  1. Hari Manev
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Radmila Manev
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Hari Manev.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Manev, H., Manev, R. Pharmacological Probing of Type 1 Autism. J Autism Dev Disord 38, 1400–1401 (2008). https://doi.org/10.1007/s10803-008-0594-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10803-008-0594-2

Keywords

Search

Navigation