Rett syndrome: Clinical peculiarities, diagnostic approach, and possible cause
- 1 March 1989
- journal article
- review article
- Published by Elsevier in Pediatric Neurology
- Vol. 5 (2) , 75-83
- https://doi.org/10.1016/0887-8994(89)90031-3
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Cerebrospinal fluid values for monoamine metabolites, γ-aminobutyric acid, and other amino compounds in Rett syndromeThe Journal of Pediatrics, 1988
- A Prospective Study of Neuropsychological Sequelae in Children With Brain TumorsJournal of Child Neurology, 1988
- VignetteJournal of Child Neurology, 1988
- Neuronal ceroid-lipofuscinoses in childhoodBrain & Development, 1988
- Review Article: Corn Oil Ketogenic Diet for Children With Intractable SeizuresJournal of Child Neurology, 1988
- Prions and Neurodegenerative DiseasesNew England Journal of Medicine, 1987
- Reduced concentrations and increased metabolism of biogenic amines in a single case of Rett-syndrome: apostmortem brain studyJournal Of Neural Transmission-Parkinsons Disease and Dementia Section, 1987
- The rett syndrome: Genetics and the futureAmerican Journal of Medical Genetics, 1986
- Chromosome findings in the rett syndrome and a test of a two-step mutation theoryAmerican Journal of Medical Genetics, 1986
- Reduction of Biogenic Amine Levels in the Rett SyndromeNew England Journal of Medicine, 1985