1.220 makale bulundu

Lrrk2 R1441C parkinsonizm klinik olarak sporadik Parkinson hastalığına benzer.

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

Haugarvoll K, Rademakers R, Kachergus JM, Nuytemans K, Ross OA, Gibson JM, Tan EK, Gaig C, Tolosa E, Goldwurm S, Guidi M, Riboldazzi G, Brown L, Walter U, Benecke R, Berg D, Gasser T, Theuns J, Pals P, Cras P, De Deyn PP, Engelborghs S, Pickut B, Uitti RJ, Foroud T, Nichols WC, Hagenah J, Klein C, Samii A, Zabetian CP, Bonifati V, Van Broeckhoven C, Farrer MJ, Wszolek ZK.

Neurology · 2008-03-12

DOI: 10.1212/01.wnl.0000304044.22253.03PMID: 18337586

Uçucu titreme ve ortak LRRK2 G2385R varyantı.

Essential tremor and the common LRRK2 G2385R variant.

Tan EK, Lee J, Lim HQ, Yuen Y, Zhao Y.

Parkinsonism Relat Disord · 2008-03-03

DOI: 10.1016/j.parkreldis.2007.12.003PMID: 18316234

Tremor baskın parkinsonizm: Klinik açıklama ve LRRK2 mutasyon taraması.

Tremor dominant parkinsonism: Clinical description and LRRK2 mutation screening.

Clarimón J, Pagonabarraga J, Paisán-Ruíz C, Campolongo A, Pascual-Sedano B, Martí-Massó JF, Singleton AB, Kulisevsky J.

Mov Disord · 2008-03-01

DOI: 10.1002/mds.21771PMID: 18098275

LRRK2-bağlantılı parkinsonizm için bir Drosophila modeli.

A Drosophila model for LRRK2-linked parkinsonism.

Liu Z, Wang X, Yu Y, Li X, Wang T, Jiang H, Ren Q, Jiao Y, Sawa A, Moran T, Ross CA, Montell C, Smith WW.

Proc Natl Acad Sci U S A · 2008-02-07

DOI: 10.1073/pnas.0708452105PMID: 18258746

SNCA, PRKN, PINK1 ve LRRK2'deki mutasyonlar için Portekiz'den Parkinson hastalığı hastalarının analizi.

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.

Bras J, Guerreiro R, Ribeiro M, Morgadinho A, Januario C, Dias M, Calado A, Semedo C, Oliveira C, Hardy J, Singleton A.

BMC Neurol · 2008-01-22

DOI: 10.1186/1471-2377-8-1PMID: 18211709

LRRK2 Gly2385Arg varyantı, anakara Çin'den Han-Çin arasında Parkinson hastalığının bir risk faktörüdür.

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

An XK, Peng R, Li T, Burgunder JM, Wu Y, Chen WJ, Zhang JH, Wang YC, Xu YM, Gou YR, Yuan GG, Zhang ZJ.

Eur J Neurol · 2008-01-14

DOI: 10.1111/j.1468-1331.2007.02052.xPMID: 18201193

Parkinson hastalığı olan Brezilyalı hastalarda G2019S LRRK2 mutasyonu: monozigotik ikizlerde fenotip.

The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.

Munhoz RP, Wakutani Y, Marras C, Teive HA, Raskin S, Werneck LC, Moreno D, Sato C, Lang AE, Rogaeva E.

Mov Disord · 2008-01-01

DOI: 10.1002/mds.21832PMID: 17999435

Brezilya'da LRRK2 mutasyonları ve Parkinson hastalığı üzerine bir çalışma.

A study of LRRK2 mutations and Parkinson's disease in Brazil.

Pimentel MM, Moura KC, Abdalla CB, Pereira JS, de Rosso AL, Nicaretta DH, Campos M, de Almeida RM, dos Santos JM, Bastos IC, Mendes MF, Maultasch H, Costa FH, Werneck AL, Santos-Rebouças CB.

Neurosci Lett · 2007-12-23

DOI: 10.1016/j.neulet.2007.12.033PMID: 18201824

Parkinson hastalığının anahtar oyuncusunun LRRK2-mikroarray ekspresyon analizinin RNA paraziti.

RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player.

Häbig K, Walter M, Poths S, Riess O, Bonin M.

Neurogenetics · 2007-12-21

DOI: 10.1007/s10048-007-0114-0PMID: 18097693

Parkinson hastalığının bir nedeni olarak LRRK2'deki mutasyonlar.

Mutations in LRRK2 as a cause of Parkinson's disease.

Giasson BI, Van Deerlin VM.

Neurosignals · 2007-12-05

DOI: 10.1159/000109764PMID: 18097165

Parkinson hastalığı olan Çin Han popülasyonunda LRRK2 Gly2385Arg varyantının yaygınlığı.

The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease.

Li C, Ting Z, Qin X, Ying W, Li B, Guo Qiang L, Jian Fang M, Jing Z, Jian Qing D, Sheng Di C.

Mov Disord · 2007-12-01

DOI: 10.1002/mds.21763PMID: 17960808

Re: The G2019S LRRK2 mutation is uncommon amongst Greek patients with familial Parkinson's disease.

Papapetropoulos S, Argyriou AA, Mitsi G, Chroni E.

Eur J Neurol · 2007-11-01

DOI: 10.1111/j.1468-1331.2007.01933.xPMID: 17956439