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The fold of alpha-synuclein fibrils.

Vilar M, Chou HT, Lührs T, Maji SK, Riek-Loher D, Verel R, Manning G, Stahlberg H, Riek R.

Proc Natl Acad Sci U S A · 2008-06-12

DOI: 10.1073/pnas.0712179105PMID: 18550842

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Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.

Healy DG, Falchi M, O'Sullivan SS, Bonifati V, Durr A, Bressman S, Brice A, Aasly J, Zabetian CP, Goldwurm S, Ferreira JJ, Tolosa E, Kay DM, Klein C, Williams DR, Marras C, Lang AE, Wszolek ZK, Berciano J, Schapira AH, Lynch T, Bhatia KP, Gasser T, Lees AJ, Wood NW, International LRRK2 Consortium.

Lancet Neurol · 2008-06-06

DOI: 10.1016/s1474-4422(08)70117-0PMID: 18539534

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LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study.

Hulihan MM, Ishihara-Paul L, Kachergus J, Warren L, Amouri R, Elango R, Prinjha RK, Upmanyu R, Kefi M, Zouari M, Sassi SB, Yahmed SB, El Euch-Fayeche G, Matthews PM, Middleton LT, Gibson RA, Hentati F, Farrer MJ.

Lancet Neurol · 2008-06-06

DOI: 10.1016/s1474-4422(08)70116-9PMID: 18539535

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LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease.

Elbaz A.

Lancet Neurol · 2008-06-06

DOI: 10.1016/s1474-4422(08)70118-2PMID: 18539536

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Ancient origin of the Parkinson disease gene LRRK2.

Marín I.

J Mol Evol · 2008-06-04

DOI: 10.1007/s00239-008-9122-4PMID: 18523712

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LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients.

Chan DK, Ng PW, Mok V, Yeung J, Fang ZM, Clarke R, Leung E, Wong L.

J Neural Transm (Vienna) · 2008-06-04

DOI: 10.1007/s00702-008-0065-0PMID: 18523722

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LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: clinical, PET, and functional studies.

Lin CH, Tzen KY, Yu CY, Tai CH, Farrer MJ, Wu RM.

J Biomed Sci · 2008-06-04

DOI: 10.1007/s11373-008-9260-0PMID: 18523869

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Impaired learning and memory in Pitx3 deficient aphakia mice: a genetic model for striatum-dependent cognitive symptoms in Parkinson's disease.

Ardayfio P, Moon J, Leung KK, Youn-Hwang D, Kim KS.

Neurobiol Dis · 2008-06-04

DOI: 10.1016/j.nbd.2008.05.017PMID: 18573342

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Commentary to "Interaction between Abeta peptide and alpha synuclein: molecular mechanisms in overlapping pathology of Alzheimer's and Parkinson's in dementia with Lewy body disease".

Mandal PK, Pettegrew JW.

Neurochem Res · 2008-06-01

DOI: 10.1007/s11064-007-9553-0PMID: 18049892

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Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.

Bogaerts V, Nuytemans K, Reumers J, Pals P, Engelborghs S, Pickut B, Corsmit E, Peeters K, Schymkowitz J, De Deyn PP, Cras P, Rousseau F, Theuns J, Van Broeckhoven C.

Hum Mutat · 2008-06-01

DOI: 10.1002/humu.20713PMID: 18401856

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Progress in the pathogenesis and genetics of Parkinson's disease.

Mizuno Y, Hattori N, Kubo S, Sato S, Nishioka K, Hatano T, Tomiyama H, Funayama M, Machida Y, Mochizuki H.

Philos Trans R Soc Lond B Biol Sci · 2008-06-01

DOI: 10.1098/rstb.2008.2273PMID: 18426756

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Review: Familial Parkinson's disease--genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease.

Schiesling C, Kieper N, Seidel K, Krüger R.

Neuropathol Appl Neurobiol · 2008-06-01

DOI: 10.1111/j.1365-2990.2008.00952.xPMID: 18447897

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

14.936 articles found

The fold of alpha-synuclein fibrils.

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study.

LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease.

Ancient origin of the Parkinson disease gene LRRK2.

LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients.

LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: clinical, PET, and functional studies.

Impaired learning and memory in Pitx3 deficient aphakia mice: a genetic model for striatum-dependent cognitive symptoms in Parkinson's disease.

Commentary to "Interaction between Abeta peptide and alpha synuclein: molecular mechanisms in overlapping pathology of Alzheimer's and Parkinson's in dementia with Lewy body disease".

Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.

Progress in the pathogenesis and genetics of Parkinson's disease.

Review: Familial Parkinson's disease--genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease.

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