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All Genetics
Citations 411-420 of 676 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease
- P. Ibáñez, E. Lohmann, P. Pollak, F. Durif, C. Tranchant, Y. Agid, A. Dürr, and A. Brice
Neurology 2004; 62: 2133-2134.
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- CLINICAL/SCIENTIFIC NOTES
A monozygotic twin pair discordant for narcolepsy and CSF hypocretin-1
- Y. Dauvilliers, S. Maret, C. Bassetti, B. Carlander, M. Billiard, J. Touchon, and M. Tafti
Neurology 2004; 62: 2137-2138.
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- CLINICAL/SCIENTIFIC NOTES
Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene
- A. D’Amico, A. Tessa, A. Sabino, E. Bertini, F. M. Santorelli, and S. Servidei
Neurology 2004; 62: 2138-2139.
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- EXPEDITED BRIEF COMMUNICATION
 -Synuclein in blood and brain from familial Parkinson disease with SNCA locus triplication
- D. W. Miller, S. M. Hague, J. Clarimon, M. Baptista, K. Gwinn-Hardy, M. R. Cookson, and A. B. Singleton
Neurology 2004; 62: 1835-1838.
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- BRIEF COMMUNICATIONS
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
- K. Jurkat-Rott, T. Freilinger, J. P. Dreier, J. Herzog, H. Göbel, G. C. Petzold, P. Montagna, T. Gasser, F. Lehmann-Horn, and M. Dichgans
Neurology 2004; 62: 1857-1861.
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- BRIEF COMMUNICATIONS
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesis
- P. Moretti, A. P. Lieberman, E. A. Wilde, B. I. Giordani, K. J. Kluin, R. A. Koeppe, S. Minoshima, D. E. Kuhl, W. K. Seltzer, and N. L. Foster
Neurology 2004; 62: 1865-1868.
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- BRIEF COMMUNICATIONS
Autosomal dominant occipital cephalocele
- Alexander G. Bassuk, David McLone, Robin Bowman, and John A. Kessler
Neurology 2004; 62: 1888-1890.
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- CLINICAL/SCIENTIFIC NOTES
Multiple meningiomas in brain and lung due to acquired mutation of the NF2 gene
- O. Eckstein, A. Stemmer-Rachamimov, F. Nunes, D. Hoch, R. Ojemann, and M. MacCollin
Neurology 2004; 62: 1904-1905.
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- CLINICAL/SCIENTIFIC NOTES
Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene)
- Robert H. Baloh, Joanna C. Jen, Gilbert Kim, and Robert W. Baloh
Neurology 2004; 62: 1905-1906.
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- CLINICAL/SCIENTIFIC NOTES
Glutathione transferase Omega class polymorphisms in Parkinson disease
- A. K. Whitbread, G. D. Mellick, P. A. Silburn, D. G. Le Couteur, and P. G. Board
Neurology 2004; 62: 1910-1911.
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