|
All Genetics
Citations 391-400 of 679 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
A limited role for DJ1 in Parkinson disease susceptibility
- D. M. Maraganore, K. Wilkes, T. G. Lesnick, K. J. Strain, M. de Andrade, W. A. Rocca, J. H. Bower, J. E. Ahlskog, S. Lincoln, and M. J. Farrer
Neurology 2004; 63: 550-553.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies
- J. Johnson, S. M. Hague, M. Hanson, A. Gibson, K. E. Wilson, E. W. Evans, A. A. Singleton, A. McInerney-Leo, R. L. Nussbaum, D. G. Hernandez, M. Gallardo, I. G. McKeith, D. J. Burn, M. Ryu, O. Hellstrom, B. Ravina, J. Eerola, R. H. Perry, E. Jaros, P. Tienari, R. Weiser, K. Gwinn-Hardy, C. M. Morris, J. Hardy, and A. B. Singleton
Neurology 2004; 63: 554-556.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL
- R. Mazzei, F. L. Conforti, P. L. Lanza, T. Sprovieri, M. R. Lupo, O. Gallo, A. Patitucci, A. Magariello, M. Caracciolo, A. L. Gabriele, F. Fera, P. Valentino, F. Bono, G. Cenacchi, G. Santoro, M. Muglia, and A. Quattrone
Neurology 2004; 63: 561-564.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma
- R. Hirano, H. Takashima, F. Umehara, H. Arimura, K. Michizono, Y. Okamoto, M. Nakagawa, C. F. Boerkoel, J. R. Lupski, M. Osame, and K. Arimura
Neurology 2004; 63: 577-580.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
FSHD in Chinese population: Characteristics of translocation and genotype-phenotype correlation
- Zhi-Ying Wu, Zhi-Qiang Wang, Shen-Xing Murong, and Ning Wang
Neurology 2004; 63: 581-583.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity
- K. Kanai, S. Hirose, H. Oguni, G. Fukuma, Y. Shirasaka, T. Miyajima, K. Wada, H. Iwasa, S. Yasumoto, M. Matsuo, M. Ito, A. Mitsudome, and S. Kaneko
Neurology 2004; 63: 329-334.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Reanalysis of genotype distributions published in Neurology between 1999 and 2002
- István Kocsis, Barna Vásárhelyi, András Györffy, and Balázs Györffy
Neurology 2004; 63: 357-358.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
DD genotype of ACE gene is a risk factor for intracerebral hemorrhage
- A. Slowik, W. Turaj, T. Dziedzic, A. Haefele, J. Pera, M. T. Malecki, L. Glodzik-Sobanska, P. Szermer, D. A. Figlewicz, and A. Szczudlik
Neurology 2004; 63: 359-361.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort
- E. K. Tan, Y. Zhao, K. Y. Puong, H. Y. Law, L. L. Chan, K. Yew, C. Tan, H. Shen, V. R. Chandran, M. L. Teoh, Y. Yih, R. Pavanni, M. C. Wong, and I. S. Ng
Neurology 2004; 63: 362-363.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Radiosurgery for cerebral arteriovenous malformations in hereditary hemorrhagic telangiectasia
- M. Maarouf, M. Runge, M. Kocher, M. Zähringer, H. Treuer, and V. Sturm
Neurology 2004; 63: 367-369.
[Abstract]
[Full text]
[PDF]
|
|
