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Journal of Autism and Developmental Disorders

Gepubliceerd in:

01-08-2008 | Letter to the Editor

Pharmacological Probing of Type 1 Autism

Auteurs: Hari Manev, Radmila Manev

Gepubliceerd in: Journal of Autism and Developmental Disorders | Uitgave 7/2008

Excerpt

Dear Editor, …

vorige artikel Brief Report: Enhanced Picture Naming in Autism

volgende artikel Scott Bellini, Building Social Relationships: A Systematic Approach to Teaching Social Interaction Skills to Children and Adolescents with Autism Spectrum Disorders and Other Social Difficulties (Textbook Edition, 1st ed.)

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.PubMedCrossRef

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.PubMedCrossRef

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.PubMedCrossRef

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

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

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.PubMedCrossRef

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.PubMedCrossRef

Titel: Pharmacological Probing of Type 1 Autism
Auteurs: Hari Manev
Radmila Manev
Publicatiedatum: 01-08-2008
Uitgeverij: Springer US
Gepubliceerd in: Journal of Autism and Developmental Disorders / Uitgave 7/2008
Print ISSN: 0162-3257
Elektronisch ISSN: 1573-3432
DOI: https://doi.org/10.1007/s10803-008-0594-2

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