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Developmental disorders
Citations 1-10 of 94 total displayed.
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Most recent content
(30 Sep 2008):
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- VIEWS AND REVIEWS
Pregnancy registries in epilepsy: A consensus statement on health outcomes
- K. J. Meador, P. B. Pennell, C. L. Harden, J. C. Gordon, T. Tomson, P. W. Kaplan, G. L. Holmes, J. A. French, W. A. Hauser, P. G. Wells, J. A. Cramer For the HOPE Work Group
Neurology 2008; 71: 1109-1117.
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Past content
(since Jan 2001):
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- ARTICLES
CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy
- M. Elia, M. Falco, R. Ferri, A. Spalletta, M. Bottitta, G. Calabrese, M. Carotenuto, S. A. Musumeci, M. Lo Giudice, and M. Fichera
Neurology 2008; 71: 997-999.
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- ARTICLES
Does lamotrigine use in pregnancy increase orofacial cleft risk relative to other malformations?
- H. Dolk, J. Jentink, M. Loane, J. Morris, L.T.W. de Jong–van den Berg On behalf of The EUROCAT Antiepileptic Drug Working Group
Neurology 2008; 71: 714-722.
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- CLINICAL/SCIENTIFIC NOTES
VERTEBRAL OSTEOMYELITIS COMPLICATING PNEUMOCOCCAL MENINGITIS
- M. C. Brouwer, J. de Gans, S.G.B. Heckenberg, H. Kuiper, H. B.M. van Lieshout, and D. van de Beek
Neurology 2008; 71: 612-613.
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- REFLECTIONS: NEUROLOGY AND THE HUMANITIES
Limelight
- Ludwig Gutmann
Neurology 2008; 71: 297-298.
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- ARTICLES
Two-year placebo-controlled trial of botulinum toxin A for leg spasticity in cerebral palsy
- A. P. Moore, R. A. Ade-Hall, C. Tudu Smith, L. Rosenbloom, H.P.J. Walsh, K. Mohamed, and P. R. Williamson
Neurology 2008; 71: 122-128.
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- ARTICLES
Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome
- J. L. Neul, P. Fang, J. Barrish, J. Lane, E. B. Caeg, E. O. Smith, H. Zoghbi, A. Percy, and D. G. Glaze
Neurology 2008; 70: 1313-1321.
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- ARTICLES
Investigating genotype–phenotype relationships in Rett syndrome using an international data set
- A. Bebbington, A. Anderson, D. Ravine, S. Fyfe, M. Pineda, N. de Klerk, B. Ben-Zeev, N. Yatawara, A. Percy, W. E. Kaufmann, and H. Leonard
Neurology 2008; 70: 868-875.
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- ARTICLES
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease
- M. Henneke, P. Combes, S. Diekmann, E. Bertini, K. Brockmann, A. P. Burlina, J. Kaiser, A. Ohlenbusch, B. Plecko, D. Rodriguez, O. Boespflug-Tanguy, and J. Gärtner
Neurology 2008; 70: 748-754.
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- VIEWS & REVIEWS
The molar tooth sign: A new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian families
- M. S. Zaki, A. Abdel-Aleem, G. Abdel-Salam, S. E. Marsh, J. L. Silhavy, A. J. Barkovich, M. E. Ross, S. N. Saleem, W. B. Dobyns, and J. G. Gleeson
Neurology 2008; 70: 556-565.
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