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All Pediatric
Citations 61-70 of 280 total displayed.
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Past content
(since Jan 2001):
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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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- EDITORIALS
Epilepsy-associated bone mineral density loss should be prevented
- Edwin Trevathan
Neurology 2008; 70: 166-167.
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- ARTICLES
Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation
- I. Sato, S. Wu, M. C. A. Ibarra, Y. K. Hayashi, H. Fujita, M. Tojo, S. J. Oh, I. Nonaka, S. Noguchi, and I. Nishino
Neurology 2008; 70: 114-122.
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- ARTICLES
Albuterol increases lean body mass in ambulatory boys with Duchenne or Becker muscular dystrophy
- C. L. Skura, E. G. Fowler, G. T. Wetzel, M. Graves, and M. J. Spencer
Neurology 2008; 70: 137-143.
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- ARTICLES
The changing natural history of spinal muscular atrophy type 1
- M. Oskoui, G. Levy, C. J. Garland, J. M. Gray, J. O’Hagen, D. C. De Vivo, and P. Kaufmann
Neurology 2007; 69: 1931-1936.
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- ARTICLES
Long-term prognosis in children with neonatal seizures: A population-based study
- Gabriel M. Ronen, David Buckley, Sharon Penney, and David L. Streiner
Neurology 2007; 69: 1816-1822.
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- EDITORIALS
Guillain-Barré syndrome: Blind men describe an elephant?
- John T. Sladky
Neurology 2007; 69: 1647-1649.
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- ARTICLES
Patterns of Guillain-Barré syndrome in children: Results from a Mexican population
- I. Nachamkin, P. Arzate Barbosa, H. Ung, C. Lobato, A. Gonzalez Rivera, P. Rodriguez, A. Garcia Briseno, L. Maria Cordero, L. Garcia Perea, J. Carlos Perez, M. Ribera, J. Veitch, C. Fitzgerald, D. Cornblath, M. Rodriguez Pinto, J. W. Griffin, H. J. Willison, A. K. Asbury, and G. M. McKhann
Neurology 2007; 69: 1665-1671.
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- ARTICLES
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan
- M. Okada, G. Kawahara, S. Noguchi, K. Sugie, K. Murayama, I. Nonaka, Y. K. Hayashi, and I. Nishino
Neurology 2007; 69: 1035-1042.
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- ARTICLES
Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease
- G. Kawahara, M. Okada, N. Morone, C. A. Ibarra, I. Nonaka, S. Noguchi, Y. K. Hayashi, and I. Nishino
Neurology 2007; 69: 1043-1049.
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