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All Genetics
Citations 261-270 of 679 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Dementia, pyramidal system involvement, and leukoencephalopathy with a presenilin 1 mutation
- M. G. Marrosu, G. Floris, G. Costa, L. Schirru, G. Spinicci, M. V. Cherchi, M. Mura, M. G. Mascia, and E. Cocco
Neurology 2006; 66: 108-111.
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- BRIEF COMMUNICATIONS
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
- M. Namekawa, P. Ribai, I. Nelson, S. Forlani, F. Fellmann, C. Goizet, C. Depienne, G. Stevanin, M. Ruberg, A. Dürr, and A. Brice
Neurology 2006; 66: 112-114.
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- VIEWS & REVIEWS
A developmental and genetic classification for malformations of cortical development
- A. J. Barkovich, R. I. Kuzniecky, G. D. Jackson, R. Guerrini, and W. B. Dobyns
Neurology 2005; 65: 1873-1887.
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- ARTICLES
Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene
- H. Jungbluth, H. Zhou, L. Hartley, B. Halliger-Keller, S. Messina, C. Longman, M. Brockington, S. A. Robb, V. Straub, T. Voit, M. Swash, A. Ferreiro, G. Bydder, C. A. Sewry, C. Müller, and F. Muntoni
Neurology 2005; 65: 1930-1935.
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- BRIEF COMMUNICATIONS
Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriers
- R. Ceravolo, A. Antonini, D. Volterrani, C. Rossi, S. Goldwurm, E. Di Maria, L. Kiferle, U. Bonuccelli, and L. Murri
Neurology 2005; 65: 1971-1973.
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- BRIEF COMMUNICATIONS
CCM3 mutations are uncommon in cerebral cavernous malformations
- D. J. Verlaan, J. Roussel, S. B. Laurent, C. E. Elger, A. M. Siegel, and G. A. Rouleau
Neurology 2005; 65: 1982-1983.
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- BRIEF COMMUNICATIONS
Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy
- Edo M. Hoogerwaard, Ieke B. Ginjaar, Egbert Bakker, and Marianne de Visser
Neurology 2005; 65: 1984-1986.
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- BRIEF COMMUNICATIONS
Comparison of family histories in FTLD subtypes and related tauopathies
- J. S. Goldman, J. M. Farmer, E. M. Wood, J. K. Johnson, A. Boxer, J. Neuhaus, C. Lomen-Hoerth, K. C. Wilhelmsen, V. M.-Y. Lee, M. Grossman, and B. L. Miller
Neurology 2005; 65: 1817-1819.
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- BRIEF COMMUNICATIONS
Two patients with COMT inhibitor–induced hepatic dysfunction and UGT1A9 genetic polymorphism
- E. Martignoni, M. Cosentino, M. Ferrari, G. Porta, E. Mattarucchi, F. Marino, S. Lecchini, and G. Nappi
Neurology 2005; 65: 1820-1822.
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- BRIEF COMMUNICATIONS
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
- S. Karamohamed, J. C. Latourelle, B. A. Racette, J. S. Perlmutter, G. F. Wooten, M. Lew, C. Klein, H. Shill, L. I. Golbe, M. H. Mark, M. Guttman, G. Nicholson, J. B. Wilk, M. Saint-Hilaire, A. L. DeStefano, R. Prakash, S. Tobin, J. Williamson, O. Suchowersky, N. Labell, B.N.J. Growdon, C. Singer, R. Watts, S. Goldwurm, G. Pezzoli, K. B. Baker, M. L. Giroux, P. P. Pramstaller, D. J. Burn, P. Chinnery, S. Sherman, P. Vieregge, I. Litvan, J. F. Gusella, R. H. Myers, and A. Parsian
Neurology 2005; 65: 1823-1825.
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