All Genetics

Citations 341-350 of 676 total displayed.

Past content (since Jan 2001):

ARTICLES
Imaging of dopaminergic dysfunction with [¹²³I]FP-CIT SPECT in early-onset parkin disease

A. Varrone, M. T. Pellecchia, M. Amboni, V. Sansone, E. Salvatore, D. Ghezzi, B. Garavaglia, A. Brice, A. Brunetti, V. Bonavita, G. De Michele, M. Salvatore, S. Pappatà, and P. Barone
Neurology 2004; 63: 2097-2103. [Abstract] [Full text] [PDF]  

ARTICLES
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis

S. Vicart, D. Sternberg, E. Fournier, F. Ochsner, P. Laforet, T. Kuntzer, B. Eymard, B. Hainque, and B. Fontaine
Neurology 2004; 63: 2120-2127. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Hereditary spastic paraplegia with frontal lobe dysfunction: A clinicopathologic study

D. Yanase, K. Komai, T. Hamaguchi, S. Okino, H. Yokoji, T. Makifuchi, H. Takano, and M. Yamada
Neurology 2004; 63: 2149-2152. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
De novo KCNQ2 mutations in patients with benign neonatal seizures

L. R.F. Claes, B. Ceulemans, D. Audenaert, L. Deprez, A. Jansen, D. Hasaerts, S. Weckx, K. G. Claeys, J. Del-Favero, C. Van Broeckhoven, and P. De Jonghe
Neurology 2004; 63: 2155-2158. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
The fragile X premutation presenting as postprandial hypotension

P. Pugliese, G. Annesi, N. Cutuli, G. Arabia, G. Nicoletti, F. Annesi, P. Tarantino, A. Gambardella, P. Valentino, M. Zappia, and A. Quattrone
Neurology 2004; 63: 2188-a-2189-a. [Full text] [PDF]  

EDITORIALS
Turning on the heat: The search for febrile seizure genes

Melodie Winawer and Dale Hesdorffer
Neurology 2004; 63: 1770-1771. [Full text] [PDF]  

ARTICLES
Linkage and association of febrile seizures to the IMPA2 gene on human chromosome 18

J. Nakayama, N. Yamamoto, K. Hamano, N. Iwasaki, M. Ohta, S. Nakahara, A. Matsui, E. Noguchi, and T. Arinami
Neurology 2004; 63: 1803-1807. [Abstract] [Full text] [PDF]  

ARTICLES
Temporal bone histopathology in dominantly inherited audiovestibular syndrome

A. Ishiyama, G. Ishiyama, I. Lopez, J. Jen, G. Kim, and R. W. Baloh
Neurology 2004; 63: 1859-1862. [Abstract] [Full text] [PDF]  

ARTICLES
Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease

H. Hochstrasser, P. Bauer, U. Walter, S. Behnke, J. Spiegel, I. Csoti, B. Zeiler, A. Bornemann, J. Pahnke, G. Becker, O. Riess, and D. Berg
Neurology 2004; 63: 1912-1917. [Abstract] [Full text] [PDF]  

ARTICLES
A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation

Joseph J. Higgins, Joanna Pucilowska, Roni Q. Lombardi, and John P. Rooney
Neurology 2004; 63: 1927-1931. [Abstract] [Full text] [PDF]  

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