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All Genetics
Citations 41-50 of 676 total displayed.
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Past content
(since Jan 2001):
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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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- ARTICLE
A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family
- Nikolay Mintchev, Eleni Zamba-Papanicolaou, Kleopas A. Kleopa, and Kyproula Christodoulou
Neurology 2009; 72: 28-32.
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- ARTICLES
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
- R. Del Bo, M. Moggio, M. Rango, S. Bonato, M. G. D’Angelo, S. Ghezzi, G. Airoldi, M. T. Bassi, M. Guglieri, L. Napoli, C. Lamperti, S. Corti, A. Federico, N. Bresolin, and G. P. Comi
Neurology 2008; 71: 1959-1966.
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- ARTICLES
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
- P. Richard, K. Gaudon, H. Haddad, A. Ben Ammar, E. Genin, S. Bauché, M. Paturneau-Jouas, J. S. Müller, H. Lochmüller, D. Grid, A. Hamri, S. Nouioua, M. Tazir, M. Mayer, C. Desnuelle, A. Barois, B. Chabrol, J. Pouget, J. Koenig, N. Gouider-Khouja, F. Hentati, B. Eymard, and D. Hantaï
Neurology 2008; 71: 1967-1972.
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