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Analysis of Cerebellar Function in Ube3a Deficient Mice Reveals Novel Genotype Specific Behaviorshot!
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10.07.2008
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Analysis of Cerebellar Function in Ube3a Deficient Mice Reveals Novel Genotype Specific Behaviors
Detlef Heck, Yu Zhao, Snigdha Roy, Mark S. LeDoux, and Lawrence T. Reiter
Hum Mol Genet e-pub April 15, 2008
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Hits: 69
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Flumazenil Positron Emiss. Tomogr. Analyses of Brain Gamma-Aminobutyric Acid Type A Receptors in AShot!
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10.07.2008
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Flumazenil Positron Emission Tomography Analyses of Brain Gamma-Aminobutyric Acid Type A Receptors in Angelman Syndrome
NAOKO ASAHINA, MD, TOHRU SHIGA, MD, PHD, KIYOSHI EGAWA, MD, HIDEAKI SHIRAISHI, MD, PHD, SHINOBU KOHSAKA, MD, PHD,
AND SHINJI SAITOH, MD, PHD
The Journal of Pediatrics • April 2008
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Behavioural flexibility in individuals with Angelman syndromehot!
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05.05.2008
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Behavioural flexibility in individuals with Angelman syndrome, Down syndrome, non-specific intellectual disability and Autism spectrum disorder R. Didden,J. Sigafoos,V. A. Green, H. Korzilius,1 C. Mouws, G. E. Lancioni, M. F. O’Reilly,L. M. G. Curfs Journal of Intellectual Disability Research doi: 10.1111/j.1365-2788.2008.01055
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Preference for water-related items in Angelmanhot!
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05.05.2008
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Preference for water-related items in Angelman syndrome, Down syndrome and non-specific intellectual disability Didden, Robert, Korzilius, Hubert, Sturmey, Peter, Lancioni, Giulio E. and Curfs, Leopold M. G. Journal of Intellectual & Developmental Disability, 33:1, 59 - 64
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SLC9A6 Mutations Cause X-Linked Ment. Retard.,Microcephaly, Epil. & Ataxia, a Phenotype Mimicking AShot!
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21.03.2008
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SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome
Gilfillan et al. The American Journal of Human Genetics (2008), doi:10.1016/j.ajhg.2008.01.013
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