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Mental retardation
Citations 21-30 of 34 total displayed.
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Past content
(since Sep 2001):
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- BRIEF COMMUNICATIONS
Proton MR spectroscopy in succinic semialdehyde dehydrogenase deficiency
- T. Ethofer, U. Seeger, U. Klose, M. Erb, B. Kardatzki, E. Kraft, G. B. Landwehrmeyer, W. Grodd, and A. Storch
Neurology 2004; 62: 1016-1018.
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- ARTICLES
Temporal cortex hypermetabolism in Down syndrome prior to the onset of dementia
- R. J. Haier, M. T. Alkire, N. S. White, M. R. Uncapher, E. Head, I. T. Lott, and C. W. Cotman
Neurology 2003; 61: 1673-1679.
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- ARTICLES
Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: A new phenotype
- N. Blau, L. Bonafé, I. Krägeloh-Mann, B. Thöny, L. Kierat, M. Häusler, and V. Ramaekers
Neurology 2003; 61: 642-647.
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- EDITORIALS
Mental retardation: X marks the spot
- Marc C. Patterson and Huda Y. Zoghbi
Neurology 2003; 61: 156-157.
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- BRIEF COMMUNICATIONS
ARX mutations in X-linked lissencephaly with abnormal genitalia
- G. Uyanik, L. Aigner, P. Martin, C. Groß, D. Neumann, H. Marschner-Schäfer, U. Hehr, and J. Winkler
Neurology 2003; 61: 232-235.
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- CLINICAL/SCIENTIFIC NOTES
Polyalanine expansion of ARX associated with cryptogenic West syndrome
- M. Kato, S. Das, K. Petras, Y. Sawaishi, and W.B. Dobyns
Neurology 2003; 61: 267-276.
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- VIEWS & REVIEWS
Clinical spectrum of succinic semialdehyde dehydrogenase deficiency
- P. L. Pearl, K. M. Gibson, M. T. Acosta, L. G. Vezina, W. H. Theodore, M. A. Rogawski, E. J. Novotny, A. Gropman, J. A. Conry, G. T. Berry, and M. Tuchman
Neurology 2003; 60: 1413-1417.
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- ARTICLES
Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1
- S.L. Hyman, D.S. Gill, E.A. Shores, A. Steinberg, P. Joy, S.V. Gibikote, and K.N. North
Neurology 2003; 60: 1139-1145.
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- ARTICLES
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts
- H. Topaloglu, M. Brockington, Y. Yuva, B. Talim, G. Haliloglu, D. Blake, S. Torelli, S.C. Brown, and F. Muntoni
Neurology 2003; 60: 988-992.
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- BRIEF COMMUNICATIONS
Late infantile Hirschsprung disease–mental retardation syndrome with a 3-bp deletion in ZFHX1B
- M. Yoneda, T. Fujita, Y. Yamada, K. Yamada, A. Fujii, T. Inagaki, H. Nakagawa, A. Shimada, M. Kishikawa, M. Nagaya, T. Azuma, M. Kuriyama, and N. Wakamatsu
Neurology 2002; 59: 1637-1640.
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