ExLibris header image
SFX Logo
Title: Frequency of the LRRK2 G2019S mutation in Italian patients affected by Parkinson's disease
Source:

Journal of Human Genetics [1434-5161] Squillaro, Tiziana yr:2007


Collapse list of basic services Basic
Full text
Full text available via Nature
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. S. Papapetropoulos et al;, K. "The G2019S LRRK2 mutation is uncommon amongst Greek patients with familial Parkinson's disease." European journal of neurology 14.10 (2007): 1088-1090. Link to Full Text for this item Link to SFX for this item
2. Lucotte, G. "Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects." Genetic testing 12.3 (2008): 333-339. Link to SFX for this item
3. Goldwurm, S. "LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample." Parkinsonism & related disorders 12.7 (2006): 410-9. Link to SFX for this item
4. Belarbi, S. "LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort." Parkinsonism & related disorders 16.10 (2010): 676-679. Link to SFX for this item
5. Giasson, Benoit I. "Mutations in LRRK2 as a Cause of Parkinson." NeuroSignals 16.1 (2008): 99-105. Link to SFX for this item
6. Aasly, Jan O. "Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease." Movement disorders 25.13 (2010): 2156-2163. Link to Full Text for this item Link to SFX for this item
7. Dekomien, G. "The LRRK2 gene in Parkinson's disease: mutation screening in patients from Germany." Journal of neurology, neurosurgery and psychiatry 77.7 (2006): 891-892. Link to Full Text for this item Link to SFX for this item
8. Kumari, U. "LRRK2 in Parkinson’s disease: genetic and clinical studies from patients." The FEBS journal 276.22 (2009): 6455-6463. Link to Full Text for this item Link to SFX for this item
9. Vermeersch, P. "Co-inheritance of haemoglobin A2' and beta-thalassaemia in cis." International Journal of Laboratory Hematology 30.4 (2008): 334-8. Link to Full Text for this item Link to SFX for this item
10. Hulihan, Mary M M. "LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study." Lancet. Neurology 7.7 (2008): 591-4. Link to SFX for this item
11. Siddiqui, Hani T S T. "Parkinson's disease in Arabs: a systematic review." Movement disorders 23.9 (2008): 1205-10. Link to Full Text for this item Link to SFX for this item
12. Gaig, C. "G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies." Journal of neurology, neurosurgery and psychiatry 78.6 (2007): 626-628. Link to Full Text for this item Link to SFX for this item
13. Sano, M. "Neuropsychological Testing in the Diagnosis of Dementia." Journal of geriatric psychiatry and neurology 19.3: 155-159. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.