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All Genetics
Citations 221-230 of 676 total displayed.
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Past content
(since Jan 2001):
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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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- BRIEF COMMUNICATIONS
Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations
- N. L. Sicotte, G. Salamon, D. W. Shattuck, N. Hageman, U. Rüb, N. Salamon, A. E. Drain, J. L. Demer, E. C. Engle, J. R. Alger, R. W. Baloh, T. Deller, and J. C. Jen
Neurology 2006; 67: 519-521.
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- CLINICAL/SCIENTIFIC NOTES
Two first-degree relatives with perimesencephalic nonaneurysmal hemorrhage
- Alide A. Tieleman, Ton A.M. van der Vliet, and Pieter E. Vos
Neurology 2006; 67: 535-536.
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- ARTICLES
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy
- M. Bugiani, S. Al Shahwan, E. Lamantea, A. Bizzi, E. Bakhsh, I. Moroni, M. R. Balestrini, G. Uziel, and M. Zeviani
Neurology 2006; 67: 273-279.
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