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All Genetics
Citations 281-290 of 676 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
- M. F. Waters, D. Fee, K. P. Figueroa, D. Nolte, U. Müller, J. Advincula, H. Coon, V. G. Evidente, and S. M. Pulst
Neurology 2005; 65: 1111-1113.
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- ARTICLES
Familial clustering of seizure types within the idiopathic generalized epilepsies
- M. R. Winawer, C. Marini, B. E. Grinton, D. Rabinowitz, S. F. Berkovic, I. E. Scheffer, and R. Ottman
Neurology 2005; 65: 523-528.
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- ARTICLES
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures
- J. C. Jen, J. Wan, T. P. Palos, B. D. Howard, and R. W. Baloh
Neurology 2005; 65: 529-534.
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- BRIEF COMMUNICATIONS
Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement
- P. Maciel, V. T. Cruz, M. Constante, I. Iniesta, M. C. Costa, S. Gallati, N. Sousa, J. Sequeiros, P. Coutinho, and M. M. Santos
Neurology 2005; 65: 603-605.
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- BRIEF COMMUNICATIONS
A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III
- K. Owada, K. Ishikawa, S. Toru, G. Ishida, M. Gomyoda, O. Tao, Y. Noguchi, K. Kitamura, I. Kondo, E. Noguchi, T. Arinami, and H. Mizusawa
Neurology 2005; 65: 629-632.
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- BRIEF COMMUNICATIONS
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome
- J. S. Müller, R. Stucka, S. Neudecker, S. Zierz, C. Schmidt, A. Huebner, H. Lochmüller, and A. Abicht
Neurology 2005; 65: 463-465.
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- CLINICAL/SCIENTIFIC NOTES
Neuroanatomy in monozygotic twins with Asperger disorder discordant for comorbid depression
- H. Yamasue, M. Ishijima, O. Abe, T. Sasaki, H. Yamada, M. Suga, M. Rogers, I. Minowa, R. Someya, H. Kurita, S. Aoki, N. Kato, and K. Kasai
Neurology 2005; 65: 491-492.
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- CLINICAL/SCIENTIFIC NOTES
Charcot–Marie–Tooth with pyramidal signs is genetically heterogeneous: Families with and without MFN2 mutations
- D. Zhu, M. L. Kennerson, G. Walizada, S. Züchner, J. M. Vance, and G. A. Nicholson
Neurology 2005; 65: 496-497.
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- EDITORIALS
Axonal Charcot–Marie–Tooth disease: The fog is slowly lifting!
- Mary M. Reilly
Neurology 2005; 65: 186-187.
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- ARTICLES
Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene
- Victoria H. Lawson, Brad V. Graham, and Kevin M. Flanigan
Neurology 2005; 65: 197-204.
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