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LRRK2 mutations and Parkinsonism.

Toft M, Mata IF, Kachergus JM, Ross OA, Farrer MJ.

Lancet · 2005-04-01

DOI: 10.1016/s0140-6736(05)74809-1PMID: 15811454

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LRRK2 mutations and Parkinsonism.

Albrecht M.

Lancet · 2005-04-01

DOI: 10.1016/s0140-6736(05)74810-8PMID: 15811455

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

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Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

Hernandez DG, Paisán-Ruíz C, McInerney-Leo A, Jain S, Meyer-Lindenberg A, Evans EW, Berman KF, Johnson J, Auburger G, Schäffer AA, Lopez GJ, Nussbaum RL, Singleton AB.

Ann Neurol · 2005-03-01

DOI: 10.1002/ana.20401PMID: 15732108

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

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Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.

Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, Gibson JM, Ross OA, Lynch T, Wiley J, Payami H, Nutt J, Maraganore DM, Czyzewski K, Styczynska M, Wszolek ZK, Farrer MJ, Toft M.

Am J Hum Genet · 2005-02-22

DOI: 10.1086/429256PMID: 15726496

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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.

Nichols WC, Pankratz N, Hernandez D, Paisán-Ruíz C, Jain S, Halter CA, Michaels VE, Reed T, Rudolph A, Shults CW, Singleton A, Foroud T, Parkinson Study Group-PROGENI investigators.

Lancet · 2005-01-01

DOI: 10.1016/s0140-6736(05)17828-3PMID: 15680455

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

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A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

Di Fonzo A, Rohé CF, Ferreira J, Chien HF, Vacca L, Stocchi F, Guedes L, Fabrizio E, Manfredi M, Vanacore N, Goldwurm S, Breedveld G, Sampaio C, Meco G, Barbosa E, Oostra BA, Bonifati V, Italian Parkinson Genetics Network.

Lancet · 2005-01-01

DOI: 10.1016/s0140-6736(05)17829-5PMID: 15680456

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

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A common LRRK2 mutation in idiopathic Parkinson's disease.

Gilks WP, Abou-Sleiman PM, Gandhi S, Jain S, Singleton A, Lees AJ, Shaw K, Bhatia KP, Bonifati V, Quinn NP, Lynch J, Healy DG, Holton JL, Revesz T, Wood NW.

Lancet · 2005-01-01

DOI: 10.1016/s0140-6736(05)17830-1PMID: 15680457

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

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.

Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan M, Uitti RJ, Calne DB, Stoessl AJ, Pfeiffer RF, Patenge N, Carbajal IC, Vieregge P, Asmus F, Müller-Myhsok B, Dickson DW, Meitinger T, Strom TM, Wszolek ZK, Gasser T.

Neuron · 2004-11-01

DOI: 10.1016/j.neuron.2004.11.005PMID: 15541309

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

1.220 articles found

LRRK2 mutations and Parkinsonism.

LRRK2 mutations and Parkinsonism.

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

A common LRRK2 mutation in idiopathic Parkinson's disease.

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.

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