|
All Genetics
Citations 1-10 of 585 total displayed.
|
Most recent content
(6 May 2008):
|
- ARTICLES
Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations
- G. A. Nicholson, C. Magdelaine, D. Zhu, S. Grew, M. M. Ryan, F. Sturtz, J. -M. Vallat, and R. A. Ouvrier
Neurology 2008; 70: 1678-1681.
[Abstract]
[Full text]
[PDF]
|
Past content
(since Jan 2001):
|
- ARTICLES
A novel PSEN2 mutation associated with a peculiar phenotype
- P. Piscopo, G. Marcon, M. R. Piras, A. Crestini, L. Malvezzi Campeggi, E. Deiana, R. Cherchi, F. Tanda, A. Deplano, N. Vanacore, F. Tagliavini, M. Pocchiari, G. Giaccone, and A. Confaloni
Neurology 2008; 70: 1549-1554.
[Abstract]
[Full text]
[PDF]
- EDITORIALS
Will my Rett syndrome patient walk, talk, and use her hands?
- Yuzhi Zhang and Berge A. Minassian
Neurology 2008; 70: 1302-1303.
[Full text]
[PDF]
- ARTICLES
Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome
- J. L. Neul, P. Fang, J. Barrish, J. Lane, E. B. Caeg, E. O. Smith, H. Zoghbi, A. Percy, and D. G. Glaze
Neurology 2008; 70: 1313-1321.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
EXTRACEPHALIC CLUSTER (CLUSTER SINE HEADACHE)
- Esma Dilli and David W. Dodick
Neurology 2008; 70: 1362-1363.
[Full text]
[PDF]
- EDITORIALS
Complicated autosomal recessive hereditary spastic paraplegia: A complex picture is emerging
- Peter Hedera and Oliver Bandmann
Neurology 2008; 70: 1375-1376.
[Full text]
[PDF]
- ARTICLES
FMR1 CGG repeat length predicts motor dysfunction in premutation carriers
- M. A. Leehey, E. Berry-Kravis, C. G. Goetz, L. Zhang, D. A. Hall, L. Li, C. D. Rice, R. Lara, J. Cogswell, A. Reynolds, L. Gane, S. Jacquemont, F. Tassone, J. Grigsby, R. J. Hagerman, and P. J. Hagerman
Neurology 2008; 70: 1397-1402.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
- K. Haugarvoll, R. Rademakers, J. M. Kachergus, K. Nuytemans, O. A. Ross, J. M. Gibson, E-K Tan, C. Gaig, E. Tolosa, S. Goldwurm, M. Guidi, G. Riboldazzi, L. Brown, U. Walter, R. Benecke, D. Berg, T. Gasser, J. Theuns, P. Pals, P. Cras, P. Paul De Deyn, S. Engelborghs, B. Pickut, R. J. Uitti, T. Foroud, W. C. Nichols, J. Hagenah, C. Klein, A. Samii, C. P. Zabetian, V. Bonifati, C. Van Broeckhoven, M. J. Farrer, and Z. K. Wszolek
Neurology 2008; 70: 1456-1460.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Myoclonus–dystonia: Clinical and electrophysiologic pattern related to SGCE mutations
- E. Roze, E. Apartis, F. Clot, N. Dorison, S. Thobois, L. Guyant-Marechal, C. Tranchant, P. Damier, D. Doummar, N. Bahi-Buisson, N. André-Obadia, D. Maltete, A. Echaniz-Laguna, Y. Pereon, Y. Beaugendre, S. Dupont, T. De Greslan, C. P. Jedynak, G. Ponsot, J. C. Dussaule, A. Brice, A. Dürr, and M. Vidailhet
Neurology 2008; 70: 1010-1016.
[Abstract]
[Full text]
[PDF]
- EDITORIALS
TRAPS and MS: Two diseases or an MS mimic?
- Subramaniam Sriram
Neurology 2008; 70: 1077-1078.
[Full text]
[PDF]
|
|
