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Genetic linkage
Citations 21-30 of 81 total displayed.
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Past content
(since Jan 2001):
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- EDITORIALS
Late-onset HMSN 2: Further evidence of genetic heterogeneity
- Peter J. Dyck
Neurology 2008; 71: 9-10.
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- ARTICLES
Late-onset hereditary axonal neuropathies
- C. L. Bennett, V. H. Lawson, K. L. Brickell, K. Isaacs, W. Seltzer, H. P. Lipe, M. D. Weiss, G. T. Carter, K. M. Flanigan, P. F. Chance, and T. D. Bird
Neurology 2008; 71: 14-20.
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- ARTICLES
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study
- J. E. Tobin, J. C. Latourelle, M. F. Lew, C. Klein, O. Suchowersky, H. A. Shill, L. I. Golbe, M. H. Mark, J. H. Growdon, G. F. Wooten, B. A. Racette, J. S. Perlmutter, R. Watts, M. Guttman, K. B. Baker, S. Goldwurm, G. Pezzoli, C. Singer, M. H. Saint-Hilaire, A. E. Hendricks, S. Williamson, M. W. Nagle, J. B. Wilk, T. Massood, J. M. Laramie, A. L. DeStefano, I. Litvan, G. Nicholson, A. Corbett, S. Isaacson, D. J. Burn, P. F. Chinnery, P. P. Pramstaller, S. Sherman, J. Al-hinti, E. Drasby, M. Nance, A. T. Moller, K. Ostergaard, R. Roxburgh, B. Snow, J. T. Slevin, F. Cambi, J. F. Gusella, and R. H. Myers
Neurology 2008; 71: 28-34.
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- ARTICLES
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4
- A. Orlacchio, C. Patrono, F. Gaudiello, C. Rocchi, V. Moschella, R. Floris, G. Bernardi, and T. Kawarai
Neurology 2008; 70: 1959-1966.
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- EDITORIALS
Hunting for genes and mutations: It's worth remembering the basics
- Thomas Gasser
Neurology 2008; 70: 1373-1374.
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- ARTICLES
Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: Redefining DYT14 as DYT5
- C. Wider, S. Melquist, M. Hauf, A. Solida, S. A. Cobb, J. M. Kachergus, J. Gass, K. D. Coon, M. Baker, A. Cannon, D. A. Stephan, D. F. Schorderet, J. Ghika, P. R. Burkhard, G. Kapatos, M. Hutton, M. J. Farrer, Z. K. Wszolek, and F.J.G. Vingerhoets
Neurology 2008; 70: 1377-1383.
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- ARTICLES
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
- K. Haugarvoll, R. Rademakers, J. M. Kachergus, K. Nuytemans, O. A. Ross, J. M. Gibson, E-K Tan, C. Gaig, E. Tolosa, S. Goldwurm, M. Guidi, G. Riboldazzi, L. Brown, U. Walter, R. Benecke, D. Berg, T. Gasser, J. Theuns, P. Pals, P. Cras, P. Paul De Deyn, S. Engelborghs, B. Pickut, R. J. Uitti, T. Foroud, W. C. Nichols, J. Hagenah, C. Klein, A. Samii, C. P. Zabetian, V. Bonifati, C. Van Broeckhoven, M. J. Farrer, and Z. K. Wszolek
Neurology 2008; 70: 1456-1460.
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- EDITORIALS
Genetics of restless legs syndrome: A burning urge to move
- Juliane Winkelmann and Bertram Müller-Myhsok
Neurology 2008; 70: 664-665.
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- VIEWS & REVIEWS
The molar tooth sign: A new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian families
- M. S. Zaki, A. Abdel-Aleem, G. Abdel-Salam, S. E. Marsh, J. L. Silhavy, A. J. Barkovich, M. E. Ross, S. N. Saleem, W. B. Dobyns, and J. G. Gleeson
Neurology 2008; 70: 556-565.
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- VIEWS & REVIEWS
Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorder
- Christine Klein and Michael G. Schlossmacher
Neurology 2007; 69: 2093-2104.
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