Concepedia

Rett Syndrome: Investigation of Nine Patients, including PET Scan

Henry G. Dunn, A. Jon Stoessl, Helena H. Ho, Patrick MacLeod, Kenneth J. Poskitt, Doris J. Doudet, Michael Schulzer, Derek Blackstock, Teresa Dobko, Ben F. Koop,

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 2002 · 32 citations · 81 references

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Abstract

Our findings suggest a mild presynaptic deficit of nigrostriatal activity in Rett syndrome.

References

81

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan et al. · Nature Genetics · 1999 · 5K citations

, , +11

MRI-PET Registration with Automated Algorithm

Roger P. Woods, John C. Mazziotta, and Simon R. Cherry · Journal of Computer Assisted Tomography · 1993 · 1.6K citations

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases

Bengt Hagberg, Jean Aicardi, Karin Ziliotto Dias et al. · Annals of Neurology · 1983 · 1.5K citations

MeCP2 Is a Transcriptional Repressor with Abundant Binding Sites in Genomic Chromatin

Xinsheng Nan, Francisco J. Campoy, Adrian Bird · Cell · 1997 · 1.3K citations · Full text

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Validity and reliability of a rating scale for the primary torsion dystonias

Robert E. Burke, Stanley Fahn, C. D. Marsden et al. · Neurology · 1985 · 1.1K citations