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All Genetics
Citations 221-230 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations
- H. Azzedine, N. Ravisé, C. Verny, A. Gabrëels-Festen, M. Lammens, D. Grid, J. M. Vallat, G. Durosier, J. Senderek, S. Nouioua, T. Hamadouche, A. Bouhouche, A. Guilbot, C. Stendel, M. Ruberg, A. Brice, N. Birouk, O. Dubourg, M. Tazir, and E. LeGuern
Neurology 2006; 67: 602-606.
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- ARTICLES
The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10
- M. Wakamiya, T. Matsuura, Y. Liu, G. C. Schuster, R. Gao, W. Xu, P. S. Sarkar, X. Lin, and T. Ashizawa
Neurology 2006; 67: 607-613.
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- ARTICLES
Autosomal dominant dystonia-plus with cerebral calcifications
- Z. K. Wszolek, Y. Baba, I. R. Mackenzie, R. J. Uitti, A. J. Strongosky, D. F. Broderick, M. C. Baker, S. Melquist, M. L. Hutton, Y. Tsuboi, J. E. Allanson, J. Carr, A. Kumar, S. M. Calne, J. Miklossy, P. L. McGeer, D. B. Calne, and A. J. Stoessl
Neurology 2006; 67: 620-625.
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- ARTICLES
Valosin-containing protein gene mutations: Clinical and neuropathologic features
- L. Guyant-Maréchal, A. Laquerrière, C. Duyckaerts, C. Dumanchin, J. Bou, F. Dugny, I. Le Ber, T. Frébourg, D. Hannequin, and D. Campion
Neurology 2006; 67: 644-651.
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- BRIEF COMMUNICATIONS
Dominantly transmitted focal dystonia in families of patients with musician’s cramp
- A. Schmidt, H. -C. Jabusch, E. Altenmüller, J. Hagenah, N. Brüggemann, K. Hedrich, R. Saunders-Pullman, S. B. Bressman, P. L. Kramer, and C. Klein
Neurology 2006; 67: 691-693.
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- BRIEF COMMUNICATIONS
Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease
- C. P. Zabetian, H. Morino, H. Ujike, M. Yamamoto, M. Oda, H. Maruyama, Y. Izumi, R. Kaji, A. Griffith, B. C. Leis, J. W. Roberts, D. Yearout, A. Samii, and H. Kawakami
Neurology 2006; 67: 697-699.
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- BRIEF COMMUNICATIONS
Occurrence of sleep disorders in the families of narcoleptic patients
- Maurice M. Ohayon and Michele L. Okun
Neurology 2006; 67: 703-705.
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- BRIEF COMMUNICATIONS
Periventricular heterotopia in fragile X syndrome
- F. Moro, T. Pisano, B. Dalla Bernardina, R. Polli, A. Murgia, L. Zoccante, F. Darra, A. Battaglia, T. Pramparo, O. Zuffardi, and R. Guerrini
Neurology 2006; 67: 713-715.
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- NEUROIMAGES
Extravasation of hyperalimentation into the spinal epidural space from a central venous line
- M. Scott Perry and Lisa Billars
Neurology 2006; 67: 715.
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- BRIEF COMMUNICATIONS
Do carriers of PYGM mutations have symptoms of McArdle disease?
- Susanne Tvede Andersen, Morten Dunø, Marianne Schwartz, and John Vissing
Neurology 2006; 67: 716-718.
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