« Previous
Next »
Parkinsonism & Related Disorders
Volume 16, Issue 2
, Pages 132-135
, February 2010
Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor
References
- Risk of action tremor in relatives of tremor-dominant and postural instability gait disorder PD. Neurology. 2003;61(7):931–936
- Neuropathological changes in essential tremor: 33 cases compared with 21 controls. Brain. 2007;130:3297–3307
- Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron. 2004;44:595–600
- Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron. 2004;44:601–607
- . The LRRK2 I2012T, G2019S, and I2020T mutations in patients with essential tremor. Neurosci Lett. 2006;407:97–100
- . Genetic analysis of LRRK2 P755L variant in Caucasian patients with parkinson's disease. Neurosci Lett. 2007;419:104–107
- . Essential tremor and the common LRRK2 G2385R variant. Parkinsonism Relat Disord. 2008;14:569–571
- Common mutations in the LRRK2 exon 41 are not responsible for essential tremor in Italian patients. Parkinsonism Relat Disord. 2008 Jun 13;[Epub ahead of print]
- . Gaucher and Parkinson diseases: unexpectedly related. Neurology. 2008;70(24):2272–2273
- Glucocerebrosidase mutations are associated with Dementia with Lewy bodies. Arch Neurol. 2009;66(5):578–583
- Elevated blood harmane (1-methyl-9H-pyrido[3,4-b]indole) concentrations in essential tremor. Neurotoxicology. 2008;29(2):294–300
- Frequency of LRRK2 mutations in Early and Late-Onset Parkinson's disease. Neurology. 2006;62:548–552
☆ The review of this paper was entirely handled by an Associate Editor, Rober Rodnitzky.
PII: S1353-8020(09)00134-5
doi: 10.1016/j.parkreldis.2009.05.008
© 2009 Elsevier Ltd. All rights reserved.
« Previous
Next »
Parkinsonism & Related Disorders
Volume 16, Issue 2
, Pages 132-135
, February 2010
