|
All Genetics
Citations 281-290 of 679 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene
- D. Haubenberger, R. E. Bittner, S. Rauch-Shorny, F. Zimprich, C. Mannhalter, L. Wagner, I. Mineva, K. Vass, E. Auff, and A. Zimprich
Neurology 2005; 65: 1304-1305.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
RAS pathway activation and an oncogenic RAS mutation in sporadic pilocytic astrocytoma
- Mukesh K. Sharma, Barbara A. Zehnbauer, Mark A. Watson, and David H. Gutmann
Neurology 2005; 65: 1335-1336.
[Full text]
[PDF]
- ARTICLES
Neuroradiologic and clinicopathologic features of oculoleptomeningeal type amyloidosis
- M. Nakamura, T. Yamashita, M. Ueda, K. Obayashi, T. Sato, T. Ikeda, Y. Washimi, T. Hirai, Y. Kuwahara, M. T. Yamamoto, M. Uchino, and Y. Ando
Neurology 2005; 65: 1051-1056.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
- M. F. Waters, D. Fee, K. P. Figueroa, D. Nolte, U. Müller, J. Advincula, H. Coon, V. G. Evidente, and S. M. Pulst
Neurology 2005; 65: 1111-1113.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Familial clustering of seizure types within the idiopathic generalized epilepsies
- M. R. Winawer, C. Marini, B. E. Grinton, D. Rabinowitz, S. F. Berkovic, I. E. Scheffer, and R. Ottman
Neurology 2005; 65: 523-528.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures
- J. C. Jen, J. Wan, T. P. Palos, B. D. Howard, and R. W. Baloh
Neurology 2005; 65: 529-534.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement
- P. Maciel, V. T. Cruz, M. Constante, I. Iniesta, M. C. Costa, S. Gallati, N. Sousa, J. Sequeiros, P. Coutinho, and M. M. Santos
Neurology 2005; 65: 603-605.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III
- K. Owada, K. Ishikawa, S. Toru, G. Ishida, M. Gomyoda, O. Tao, Y. Noguchi, K. Kitamura, I. Kondo, E. Noguchi, T. Arinami, and H. Mizusawa
Neurology 2005; 65: 629-632.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome
- J. S. Müller, R. Stucka, S. Neudecker, S. Zierz, C. Schmidt, A. Huebner, H. Lochmüller, and A. Abicht
Neurology 2005; 65: 463-465.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Neuroanatomy in monozygotic twins with Asperger disorder discordant for comorbid depression
- H. Yamasue, M. Ishijima, O. Abe, T. Sasaki, H. Yamada, M. Suga, M. Rogers, I. Minowa, R. Someya, H. Kurita, S. Aoki, N. Kato, and K. Kasai
Neurology 2005; 65: 491-492.
[Full text]
[PDF]
|
|
