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All Genetics
Citations 41-50 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
APOE  2 is associated with intact cognition but increased Alzheimer pathology in the oldest old
- Daniel J. Berlau, María M. Corrada, Elizabeth Head, and Claudia H. Kawas
Neurology 2009; 72: 829-834.
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- ARTICLES
Age at intracranial aneurysm rupture among generations: Familial Intracranial Aneurysm Study
- D. Woo, R. Hornung, L. Sauerbeck, R. Brown, I. Meissner, J. Huston, T. Foroud, J. Broderick For the FIA Investigators
Neurology 2009; 72: 695-698.
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- ARTICLES
Fat metabolism during exercise in patients with McArdle disease
- M. C. Ørngreen, T. D. Jeppesen, S. Tvede Andersen, T. Taivassalo, S. Hauerslev, N. Preisler, R. G. Haller, G. van Hall, and J. Vissing
Neurology 2009; 72: 718-724.
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- ARTICLES
A novel Frabin (FGD4) nonsense mutation p.R275X associated with phenotypic variability in CMT4H
- Henry Houlden, Simon Hammans, Haider Katifi, and Mary M. Reilly
Neurology 2009; 72: 617-620.
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- VIEWS AND REVIEWS
A neurologist’s guide to genome-wide association studies
- S. A. Mullen, D. E. Crompton, P. W. Carney, I. Helbig, and S. F. Berkovic
Neurology 2009; 72: 558-565.
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- ARTICLES
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
- A. Di Fonzo, M.C.J. Dekker, P. Montagna, A. Baruzzi, E. H. Yonova, L. Correia Guedes, A. Szczerbinska, T. Zhao, L. O.M. Dubbel-Hulsman, C. H. Wouters, E. de Graaff, W. J.G. Oyen, E. J. Simons, G. J. Breedveld, B. A. Oostra, M. W. Horstink, and V. Bonifati
Neurology 2009; 72: 240-245.
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- VIEWS AND REVIEWS
Genetics of epilepsy syndromes starting in the first year of life
- Liesbet Deprez, An Jansen, and Peter De Jonghe
Neurology 2009; 72: 273-281.
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- CLINICAL/SCIENTIFIC NOTES
INFLAMMATORY PSEUDOTUMOR ASSOCIATED WITH HIV, JCV, AND IMMUNE RECONSTITUTION SYNDROME
- A. Gonzalez-Duarte, S. Sullivan, G. J. Sips, T. Naidich, G. Kleinman, J. Murray, S. Morgello, I. Germano, M. Mullen, and D. Simpson
Neurology 2009; 72: 289-290.
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- EDITORIALS
Parkinson disease(s): Is "Parkin disease" a distinct clinical entity?
- Christine Klein and Katja Lohmann
Neurology 2009; 72: 106-107.
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- ARTICLES
A multidisciplinary study of patients with early-onset PD with and without parkin mutations
- E. Lohmann, S. Thobois, S. Lesage, E. Broussolle, S. Tezenas du Montcel, M. -J. Ribeiro, P. Remy, A. Pelissolo, B. Dubois, L. Mallet, P. Pollak, Y. Agid, A. Brice, and The French Parkinson's Disease Genetics Study Group
Neurology 2009; 72: 110-116.
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