Scientific Literature Search

Source record

Penetrance of LRRK2 mutations in familial Parkinson disease.

Check source for author details

Nat Clin Pract Neurol · 2009-03-01

PMID: 20408266

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies.

Gaig C, Martí MJ, Ezquerra M, Cardozo A, Rey MJ, Tolosa E.

BMJ Case Rep · 2009-01-23

DOI: 10.1136/bcr.08.2008.0632PMID: 21686713

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

The small GTPase activity of the ROC domain from LRRK2, a Parkinson's disease related protein.

Fu QS, Song AX, Li SX, Hu HY.

Protein Pept Lett · 2009-01-01

DOI: 10.2174/092986609789839386PMID: 20001906

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

Test for LRRK2 mutations in patients with Parkinson's disease.

Healy DG, Wood NW, Schapira AH.

Pract Neurol · 2008-12-01

DOI: 10.1136/jnnp.2008.162420PMID: 19015299

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

Emerging pathways in genetic Parkinson's disease: tangles, Lewy bodies and LRRK2.

Devine MJ, Lewis PA.

FEBS J · 2008-12-01

DOI: 10.1111/j.1742-4658.2008.06707.xPMID: 19021752

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

[Advance of the study on LRRK2 gene in Parkinson's disease].

Zhang Y, Chen S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi · 2008-12-01

PMID: 19065525

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

Co-occurrence of sporadic parkinsonism and late-onset Alzheimer's disease in a Brazilian male with the LRRK2 p.G2019S mutation.

Santos-Rebouças CB, Abdalla CB, Baldi FJ, Martins PA, Corrêa JC, Gonçalves AP, Cunha MS, Borges MB, Pereira JS, Laks J, Pimentel MM.

Genet Test · 2008-12-01

DOI: 10.1089/gte.2008.0042PMID: 19072560

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

Genetic factors influencing age at onset in LRRK2-linked Parkinson disease.

Golub Y, Berg D, Calne DB, Pfeiffer RF, Uitti RJ, Stoessl AJ, Wszolek ZK, Farrer MJ, Mueller JC, Gasser T, Fuchs J.

Parkinsonism Relat Disord · 2008-11-28

DOI: 10.1016/j.parkreldis.2008.10.008PMID: 19041274

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity.

Gorostidi A, Ruiz-Martínez J, Lopez de Munain A, Alzualde A, Martí Massó JF.

Neurogenetics · 2008-11-20

DOI: 10.1007/s10048-008-0162-0PMID: 19020907

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Open access

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.

Latourelle JC, Sun M, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA, Singer C, Goldwurm S, Pezzoli G, Zini M, Saint-Hilaire MH, Hendricks AE, Williamson S, Nagle MW, Wilk JB, Massood T, Huskey KW, Laramie JM, DeStefano AL, Baker KB, Itin I, Litvan I, Nicholson G, Corbett A, Nance M, Drasby E, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Al-hinti J, Moller AT, Ostergaard K, Sherman SJ, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH.

BMC Med · 2008-11-05

DOI: 10.1186/1741-7015-6-32PMID: 18986508

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Open access

LRRK2 in Parkinson's disease - drawing the curtain of penetrance: a commentary.

Krüger R.

BMC Med · 2008-11-05

DOI: 10.1186/1741-7015-6-33PMID: 18986509

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Source record

LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay.

Mata IF, Cosentino C, Marca V, Torres L, Mazzetti P, Ortega O, Raggio V, Aljanati R, Buzó R, Yearout D, Dieguez E, Zabetian CP.

Parkinsonism Relat Disord · 2008-11-05

DOI: 10.1016/j.parkreldis.2008.09.002PMID: 18980856

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Article details View source ↗

Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

1.241 articles found

Penetrance of LRRK2 mutations in familial Parkinson disease.

G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies.

The small GTPase activity of the ROC domain from LRRK2, a Parkinson's disease related protein.

Test for LRRK2 mutations in patients with Parkinson's disease.

Emerging pathways in genetic Parkinson's disease: tangles, Lewy bodies and LRRK2.

[Advance of the study on LRRK2 gene in Parkinson's disease].

Co-occurrence of sporadic parkinsonism and late-onset Alzheimer's disease in a Brazilian male with the LRRK2 p.G2019S mutation.

Genetic factors influencing age at onset in LRRK2-linked Parkinson disease.

LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity.

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.

LRRK2 in Parkinson's disease - drawing the curtain of penetrance: a commentary.

LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay.

Filters