NeuralCipher Source record
LRRK2 mutations in a clinic-based cohort of Parkinson's disease.
DOI: 10.1111/j.1468-1331.2006.01472.xPMID: 17116211
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
1.220 articles found
“Parkinson LRRK2” Clear search
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A novel P755L mutation in LRRK2 gene associated with Parkinson's disease.
DOI: 10.1097/wnr.0b013e328010521cPMID: 17179858
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
LRRK2 in Parkinson's disease and dementia with Lewy bodies.
DOI: 10.1186/1750-1326-1-17PMID: 17137507
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Genetic analysis of LRRK2 mutations in patients with Parkinson disease.
DOI: 10.1016/j.jns.2006.09.017PMID: 17097110
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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The familial Parkinsonism gene LRRK2 regulates neurite process morphology.
DOI: 10.1016/j.neuron.2006.10.008PMID: 17114044
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Identification of a common genetic risk variant (LRRK2 Gly2385Arg) in Parkinson's disease.
DOI: 10.47102/annals-acadmedsg.v35n11p840PMID: 17160203
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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LRRK2 mutations and Parkinson's disease in Sardinia--A Mediterranean genetic isolate.
DOI: 10.1016/j.parkreldis.2006.06.010PMID: 17064949
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.
DOI: 10.1212/01.wnl.0000244345.49809.36PMID: 17050822
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients.
DOI: 10.1016/j.neulet.2006.04.052PMID: 17052850
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Leucine-rich repeat kinase 2 (LRRK2) mutations in a Swedish Parkinson cohort and a healthy nonagenarian.
DOI: 10.1002/mds.21016PMID: 16817197
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Parkinsonism, Lrrk2 G2019S, and tau neuropathology.
DOI: 10.1212/01.wnl.0000240220.33950.0cPMID: 17060589
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.
DOI: 10.1007/s00439-006-0268-0PMID: 17019612
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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