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The Nina Foundation for Angelman Syndrome
Fundación Nina arrow Artículos Científicos (inglés)

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file icon Analysis of Cerebellar Function in Ube3a Deficient Mice Reveals Novel Genotype Specific Behaviorshot!
10.07.2008
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
Hits: 220
file icon Flumazenil Positron Emiss. Tomogr. Analyses of Brain Gamma-Aminobutyric Acid Type A Receptors in AShot!
10.07.2008

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

Hits: 214
file icon Behavioural flexibility in individuals with Angelman syndromehot!
05.05.2008
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
Hits: 449
file icon Preference for water-related items in Angelmanhot!
05.05.2008

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

Hits: 410
file icon SLC9A6 Mutations Cause X-Linked Ment. Retard.,Microcephaly, Epil. & Ataxia, a Phenotype Mimicking AShot!
21.03.2008

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

 

Hits: 590
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