Scientific Literature Search

Source record

The Parkinson disease gene LRRK2: evolutionary and structural insights.

Marín I.

Mol Biol Evol · 2006-09-11

DOI: 10.1093/molbev/msl114PMID: 16966681

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

Article details View source ↗

Source record

Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease.

Hedrich K, Winkler S, Hagenah J, Kabakci K, Kasten M, Schwinger E, Volkmann J, Pramstaller PP, Kostic V, Vieregge P, Klein C.

Mov Disord · 2006-09-01

DOI: 10.1002/mds.20990PMID: 16758483

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

Article details View source ↗

Source record

The pleomorphic pathology of inherited Parkinson's disease: lessons from LRRK2.

Bonifati V.

Curr Neurol Neurosci Rep · 2006-09-01

DOI: 10.1007/s11910-996-0013-zPMID: 16928343

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

Article details View source ↗

Source record

The importance of LRRK2 mutations in Parkinson disease.

Schapira AH.

Arch Neurol · 2006-09-01

DOI: 10.1001/archneur.63.9.1225PMID: 16966498

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

Article details View source ↗

Source record

LRRK2 gene and tremor-dominant parkinsonism.

Haugarvoll K, Uitti RJ, Farrer MJ, Wszolek ZK.

Arch Neurol · 2006-09-01

DOI: 10.1001/archneur.63.9.1346-bPMID: 16966525

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

Article details View source ↗

Source record

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Zabetian CP, Hutter CM, Yearout D, Lopez AN, Factor SA, Griffith A, Leis BC, Bird TD, Nutt JG, Higgins DS, Roberts JW, Kay DM, Edwards KL, Samii A, Payami H.

Am J Hum Genet · 2006-08-17

DOI: 10.1086/508025PMID: 16960813

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

Article details View source ↗

Source record

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.

Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, Hatano Y, Wang M, Imamichi Y, Mizoguchi K, Miyajima H, Obata F, Toda T, Farrer MJ, Mizuno Y, Hattori N.

Mov Disord · 2006-08-01

DOI: 10.1002/mds.20886PMID: 16622854

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

Article details View source ↗

Source record

Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.

Marongiu R, Ghezzi D, Ialongo T, Soleti F, Elia A, Cavone S, Albanese A, Altavista MC, Barone P, Brusa L, Cortelli P, Petrozzi L, Scaglione C, Stanzione P, Tinazzi M, Zeviani M, Dallapiccola B, Bentivoglio AR, Valente EM, Garavaglia B, Italian PD Study Group.

Mov Disord · 2006-08-01

DOI: 10.1002/mds.20890PMID: 16622859

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

Article details View source ↗

Source record

Striatal dopamine transporter binding in Parkinson's disease associated with the LRRK2 Gly2019Ser mutation.

Isaias IU, Benti R, Goldwurm S, Zini M, Cilia R, Gerundini P, Di Fonzo A, Bonifati V, Pezzoli G, Antonini A.

Mov Disord · 2006-08-01

DOI: 10.1002/mds.20909PMID: 16671078

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

Article details View source ↗

Source record

LRRK2: a link between familial and sporadic Parkinson's disease?

Lesage S, Dürr A, Brice A.

Pathol Biol (Paris) · 2006-08-01

DOI: 10.1016/j.patbio.2006.06.001PMID: 16884863

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

Article details View source ↗

Source record

Parkinson's disease: the LRRK2-G2019S mutation: opening a novel era in Parkinson's disease genetics.

Bonifati V.

Eur J Hum Genet · 2006-07-12

DOI: 10.1038/sj.ejhg.5201695PMID: 16835587

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

Article details View source ↗

Source record

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease.

Tan EK, Skipper L, Chua E, Wong MC, Pavanni R, Bonnard C, Kolatkar P, Liu JJ.

Mov Disord · 2006-07-01

DOI: 10.1002/mds.20875PMID: 16602113

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.

1.220 articles found

The Parkinson disease gene LRRK2: evolutionary and structural insights.

Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease.

The pleomorphic pathology of inherited Parkinson's disease: lessons from LRRK2.

The importance of LRRK2 mutations in Parkinson disease.

LRRK2 gene and tremor-dominant parkinsonism.

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.

Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.

Striatal dopamine transporter binding in Parkinson's disease associated with the LRRK2 Gly2019Ser mutation.

LRRK2: a link between familial and sporadic Parkinson's disease?

Parkinson's disease: the LRRK2-G2019S mutation: opening a novel era in Parkinson's disease genetics.

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease.

Filters