Advances in the Genetics of Human Tremor
Publisher
Springer New York
Reference125 articles.
1. Abeliovich A, Schmitz Y, Fariñas I, Choi-Lundberg D, Ho WH, Castillo PE, Shinsky N, Verdugo JM, Armanini M, Ryan A, Hynes M, Phillips H, Sulzer D, Rosenthal A. Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system. Neuron. 2000;25(1):239–52. 2. Annesi F, De Marco EV, Rocca FE, Nicoletti A, Pugliese P, Nicoletti G, Arabia G, Tarantino P, De Mari M, Lamberti P, Gallerini S, Marconi R, Epifanio A, Morgante L, Cozzolino A, Barone P, Torchia G, Zappia M, Annesi G, Quattrone A. Association study between the LINGO1 gene and Parkinson’s disease in the Italian population. Parkinsonism Relat Disord. 2011;17(8):638–41. 3. Auer-Grumbach M, Strasser-Fuchs S, Wagner K, Körner E, Fazekas F. Roussy–Lévy syndrome is a phenotypic variant of Charcot-Marie-Tooth syndrome IA associated with a duplication on chromosome 17p11.2. J Neurol Sci. 1998;154(1):72–5. 4. Bademci G, Edwards TL, Torres AL, Scott WK, Züchner S, Martin ER, Vance JM, Wang L. A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease. Hum Mutat. 2010;31(10):E1767–71. 5. Barbieri F, Filla A, Ragno M, Crisci C, Santoro L, Corona M, Campanella G. Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome. Can J Neurol Sci. 1984;11(4 Suppl):534–40.
|
|