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Neurology
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Developmental disorders

Citations 1-10 of 94 total displayed.

Most recent content (30 Sep 2008):

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. [Abstract] [Full text] [PDF]  

Past content (since Jan 2001):

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Full text] [PDF]  

REFLECTIONS: NEUROLOGY AND THE HUMANITIES
Limelight
Ludwig Gutmann
Neurology 2008; 71: 297-298. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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 Pediatric
 All Pediatric
 Developmental disorders
 Neonatal
 Mental retardation
 Child psychiatry
 Pediatric depression
 Pediatric conversion
 Adolescence
 Autism


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