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All Genetics
Citations 371-380 of 676 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy
- F. Zimprich, R. Sunder-Plassmann, E. Stogmann, A. Gleiss, A. Dal-Bianco, A. Zimprich, S. Plumer, C. Baumgartner, and C. Mannhalter
Neurology 2004; 63: 1087-1089.
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- BRIEF COMMUNICATIONS
Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia
- M. Fichera, M. Lo Giudice, M. Falco, M. Sturnio, S. Amata, O. Calabrese, S. Bigoni, E. Calzolari, and M. Neri
Neurology 2004; 63: 1108-1110.
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- BRIEF COMMUNICATIONS
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy
- P. Prandini, A. Berardinelli, M. Fanin, F. Morello, E. Zardini, A. Pichiecchio, C. Uggetti, G. Lanzi, C. Angelini, and E. Pegoraro
Neurology 2004; 63: 1118-1121.
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- CLINICAL/SCIENTIFIC NOTES
Gene–gene interaction between interleukin-6 and interleukin-10 reduces AD risk
- J. Infante, C. Sanz, J. L. Fernández-Luna, J. Llorca, J. Berciano, and O. Combarros
Neurology 2004; 63: 1135-1136.
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- CLINICAL/SCIENTIFIC NOTES
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation
- E. E. Kors, A. Melberg, K. R.J. Vanmolkot, E. Kumlien, J. Haan, R. Raininko, R. Flink, H. B. Ginjaar, R. R. Frants, M. D. Ferrari, and A. M.J.M. van den Maagdenberg
Neurology 2004; 63: 1136-1137.
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- EDITORIALS
How not to synthesize synuclein
- Kirk C. Wilhelmsen
Neurology 2004; 63: 770-771.
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- ARTICLES
ß-Synuclein gene alterations in dementia with Lewy bodies
- H. Ohtake, P. Limprasert, Y. Fan, O. Onodera, A. Kakita, H. Takahashi, L. T. Bonner, D. W. Tsuang, I. V.J. Murray, V. M.-Y. Lee, J. Q. Trojanowski, A. Ishikawa, J. Idezuka, M. Murata, T. Toda, T. D. Bird, J. B. Leverenz, S. Tsuji, and A. R. La Spada
Neurology 2004; 63: 805-811.
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- BRIEF COMMUNICATIONS
Infantile neuroaxonal dystrophy and pantothenate kinase-associated neurodegeneration: Locus heterogeneity
- K. Hörtnagel, N. Nardocci, G. Zorzi, B. Garavaglia, E. Botz, T. Meitinger, and T. Klopstock
Neurology 2004; 63: 922-924.
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- BRIEF COMMUNICATIONS
Aprataxin gene mutations in Tunisian families
- R. Amouri, M. -C. Moreira, M. Zouari, G. El Euch, C. Barhoumi, M. Kefi, S. Belal, M. Koenig, and F. Hentati
Neurology 2004; 63: 928-929.
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- CLINICAL/SCIENTIFIC NOTES
Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians
- G. Stevanin, A. Durr, C. Dussert, C. Penet, and A. Brice
Neurology 2004; 63: 936.
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