|
All Genetics
Citations 391-400 of 676 total displayed.
|
Past content
(since Jan 2001):
|
- 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]
- ARTICLES
Germline and mosaic mutations of FLN1 in men with periventricular heterotopia
- R. Guerrini, D. Mei, S. Sisodiya, F. Sicca, B. Harding, Y. Takahashi, T. Dorn, A. Yoshida, J. Campistol, G. Krämer, F. Moro, W. B. Dobyns, and E. Parrini
Neurology 2004; 63: 51-56.
[Abstract]
[Full text]
[PDF]
- ARTICLES
PET evidence for a role of the basal ganglia in patients with ring chromosome 20 epilepsy
- A. Biraben, F. Semah, M. -J. Ribeiro, G. Douaud, P. Remy, and A. Depaulis
Neurology 2004; 63: 73-77.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Detection of novel mutations in the SMN Tudor domain in type I SMA patients
- I. Cuscó, M. Jesus Barceló, E. del Río, M. Baiget, and E. F. Tizzano
Neurology 2004; 63: 146-149.
[Abstract]
[Full text]
[PDF]
|
|
