|
All Genetics
Citations 51-60 of 676 total displayed.
|
Past content
(since Jan 2001):
|
- ARTICLES
Altered language processing in autosomal dominant partial epilepsy with auditory features
- R. Ottman, L. Rosenberger, A. Bagic, K. Kamberakis, E. K. Ritzl, A. M. Wohlschlager, S. Shamim, S. Sato, C. Liew, W. D. Gaillard, E. Wiggs, M. M. Berl, P. Reeves-Tyer, E. H. Baker, J. A. Butman, and W. H. Theodore
Neurology 2008; 71: 1973-1980.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Is olfactory impairment in Parkinson disease related to phenotypic or genotypic characteristics?
- D. Verbaan, S. Boesveldt, S. M. van Rooden, M. Visser, J. Marinus, M. G. Macedo, Y. Fang, P. Heutink, H. W. Berendse, and J. J. van Hilten
Neurology 2008; 71: 1877-1882.
[Abstract]
[Full text]
[PDF]
- ARTICLES
New morphologic and genetic findings in cap disease associated with β-tropomyosin (TPM2) mutations
- M. Ohlsson, S. Quijano-Roy, N. Darin, G. Brochier, E. Lacène, D. Avila-Smirnow, M. Fardeau, A. Oldfors, and H. Tajsharghi
Neurology 2008; 71: 1896-1901.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Progression of dopaminergic dysfunction in a LRRK2 kindred: A multitracer PET study
- R. Nandhagopal, E. Mak, M. Schulzer, J. McKenzie, S. McCormick, V. Sossi, T. J. Ruth, A. Strongosky, M. J. Farrer, Z. K. Wszolek, and A. J. Stoessl
Neurology 2008; 71: 1790-1795.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Multiple sclerosis and the TNFRSF1A R92Q mutation: Clinical characteristics of 21 cases
- T. Kümpfel, L-A Hoffmann, H. Pellkofer, W. Pöllmann, W. Feneberg, R. Hohlfeld, and P. Lohse
Neurology 2008; 71: 1812-1820.
[Abstract]
[Full text]
[PDF]
- EDITORIALS
Hereditary motor neuropathy and heat shock proteins: A shocking transformation
- Clifton Gooch and Michael Shy
Neurology 2008; 71: 1656-1657.
[Full text]
[PDF]
- ARTICLES
Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2
- H. Houlden, M. Laura, F. Wavrant–De Vrièze, J. Blake, N. Wood, and M. M. Reilly
Neurology 2008; 71: 1660-1668.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
- C. H. Lin, E. K. Tan, M. L. Chen, L. C. Tan, H. Q. Lim, G. S. Chen, and R. M. Wu
Neurology 2008; 71: 1727-1732.
[Abstract]
[Full text]
[PDF]
- EDITORIALS
Sporadically occurring neurologic disease: HSP genes and apparently sporadic spastic paraplegia
- John K. Fink
Neurology 2008; 71: 1468-1469.
[Full text]
[PDF]
- ARTICLES
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes
- F. Brugman, H. Scheffer, J.H.J. Wokke, W. M. Nillesen, M. de Visser, E. Aronica, J. H. Veldink, and L. H. van den Berg
Neurology 2008; 71: 1500-1505.
[Abstract]
[Full text]
[PDF]
|
|
