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All Genetics
Citations 1-10 of 610 total displayed.
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Most recent content
(7 Oct 2008):
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- ARTICLES
Progranulin variability has no major role in Parkinson disease genetic etiology
- K. Nuytemans, P. Pals, K. Sleegers, S. Engelborghs, E. Corsmit, K. Peeters, B. Pickut, M. Mattheijssens, P. Cras, P. P. De Deyn, J. Theuns, and C. Van Broeckhoven
Neurology 2008; 71: 1147-1151.
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- SPECIAL ARTICLES
Invited Article: The Alzheimer disease–frontotemporal lobar degeneration spectrum
- Julie van der Zee, Kristel Sleegers, and Christine Van Broeckhoven
Neurology 2008; 71: 1191-1197.
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Past content
(since Jan 2001):
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- ARTICLES
CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy
- M. Elia, M. Falco, R. Ferri, A. Spalletta, M. Bottitta, G. Calabrese, M. Carotenuto, S. A. Musumeci, M. Lo Giudice, and M. Fichera
Neurology 2008; 71: 997-999.
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- CLINICAL/SCIENTIFIC NOTES
TWO SETS OF IDENTICAL TWINS WITH CERVICAL ARTERY DISSECTION CONCORDANT FOR TEMPORAL ARTERY PATHOLOGY
- W. Völker, G. Kuhlenbäumer, R. Dittrich, S. Appenzeller, S. Grewe, D. Maintz, W. Heindel, K. H. Grotemeyer, and E. B. Ringelstein
Neurology 2008; 71: 1035-1037.
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- ARTICLES
PINK1 mutations and parkinsonism
- L. Ishihara-Paul, M. M. Hulihan, J. Kachergus, R. Upmanyu, L. Warren, R. Amouri, R. Elango, R. K. Prinjha, A. Soto, M. Kefi, M. Zouari, S. B. Sassi, S. B. Yahmed, G. El Euch-Fayeche, P. M. Matthews, L. T. Middleton, R. A. Gibson, F. Hentati, and M. J. Farrer
Neurology 2008; 71: 896-902.
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- ARTICLES
Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids
- J. A. Van Gerpen, C. Wider, D. F. Broderick, D. W. Dickson, L. A. Brown, and Z. K. Wszolek
Neurology 2008; 71: 925-929.
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- EDITORIALS
Parent of origin in multiple sclerosis: Understanding inheritance in complex neurologic diseases
- Orhun H. Kantarci and Anne Spurkland
Neurology 2008; 71: 786-787.
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- ARTICLES
Distinct muscle imaging patterns in myofibrillar myopathies
- D. Fischer, R. A. Kley, K. Strach, C. Meyer, T. Sommer, K. Eger, A. Rolfs, W. Meyer, A. Pou, J. Pradas, C. M. Heyer, A. Grossmann, A. Huebner, W. Kress, J. Reimann, R. Schröder, B. Eymard, M. Fardeau, B. Udd, L. Goldfarb, M. Vorgerd, and M. Olivé
Neurology 2008; 71: 758-765.
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- CLINICAL/SCIENTIFIC NOTES
KING-DENBOROUGH SYNDROME CAUSED BY A NOVEL MUTATION IN THE RYANODINE RECEPTOR GENE
- C. E. D’Arcy, A. Bjorksten, E. M. Yiu, A. Bankier, R. Gillies, C. A. McLean, L. K. Shield, and M. M. Ryan
Neurology 2008; 71: 776-777.
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- ARTICLES
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
- N. Brouwers, K. Sleegers, S. Engelborghs, S. Maurer-Stroh, I. Gijselinck, J. van der Zee, B. A. Pickut, M. Van den Broeck, M. Mattheijssens, K. Peeters, J. Schymkowitz, F. Rousseau, J. -J. Martin, M. Cruts, P. P. De Deyn, and C. Van Broeckhoven
Neurology 2008; 71: 656-664.
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