Scientific Literature Search

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A case of restless leg syndrome in a family with LRRK2 gene mutation.

De Rosa A, Guacci A, Peluso S, Del Gaudio L, Massarelli M, Barbato S, Criscuolo C, De Michele G.

Int J Neurosci · 2013-02-04

DOI: 10.3109/00207454.2012.756485PMID: 23227859

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Immunotherapy for neurodegenerative diseases: focus on α-synucleinopathies.

Valera E, Masliah E.

Pharmacol Ther · 2013-02-04

DOI: 10.1016/j.pharmthera.2013.01.013PMID: 23384597

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Selective expression of α-synuclein-immunoreactivity in vesicular acetylcholine transporter-immunoreactive axons in the guinea pig rectum and human colon.

Sharrad DF, de Vries E, Brookes SJ.

J Comp Neurol · 2013-02-01

DOI: 10.1002/cne.23198PMID: 22821666

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Alpha-synuclein pathology and axonal degeneration of the peripheral motor nerves innervating pharyngeal muscles in Parkinson disease.

Mu L, Sobotka S, Chen J, Su H, Sanders I, Adler CH, Shill HA, Caviness JN, Samanta JE, Beach TG, Arizona Parkinson’s Disease Consortium.

J Neuropathol Exp Neurol · 2013-02-01

DOI: 10.1097/nen.0b013e3182801cdePMID: 23334595

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[Genetics of movement disorders].

Lohmann K, Brockmann K.

Nervenarzt · 2013-02-01

DOI: 10.1007/s00115-012-3638-yPMID: 23354823

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Mapping the subcellular distribution of α-synuclein in neurons using genetically encoded probes for correlated light and electron microscopy: implications for Parkinson's disease pathogenesis.

Boassa D, Berlanga ML, Yang MA, Terada M, Hu J, Bushong EA, Hwang M, Masliah E, George JM, Ellisman MH.

J Neurosci · 2013-02-01

DOI: 10.1523/jneurosci.2898-12.2013PMID: 23392688

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RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk.

MacLeod DA, Rhinn H, Kuwahara T, Zolin A, Di Paolo G, McCabe BD, Marder KS, Honig LS, Clark LN, Small SA, Abeliovich A.

Neuron · 2013-02-01

DOI: 10.1016/j.neuron.2012.11.033PMID: 23395371

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Parkinson's disease and α-synuclein: passing it on.

Skaper SD.

CNS Neurol Disord Drug Targets · 2013-02-01

DOI: 10.2174/1871527311312010002PMID: 23394529

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APOE ε4 increases risk for dementia in pure synucleinopathies.

Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Trojanowski JQ, Weintraub D, Chen-Plotkin AS, Irwin DJ, Rick J, Schellenberg GD, Watson GS, Kukull W, Nelson PT, Jicha GA, Neltner JH, Galasko D, Masliah E, Quinn JF, Chung KA, Yearout D, Mata IF, Wan JY, Edwards KL, Montine TJ, Zabetian CP.

JAMA Neurol · 2013-02-01

DOI: 10.1001/jamaneurol.2013.600PMID: 23407718

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C9orf72 repeat expansions are a rare genetic cause of parkinsonism.

Lesage S, Le Ber I, Condroyer C, Broussolle E, Gabelle A, Thobois S, Pasquier F, Mondon K, Dion PA, Rochefort D, Rouleau GA, Dürr A, Brice A, French Parkinson’s Disease Genetics Study Group.

Brain · 2013-02-01

DOI: 10.1093/brain/aws357PMID: 23413259

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A progressive dopaminergic phenotype associated with neurotoxic conversion of α-synuclein in BAC-transgenic rats.

Nuber S, Harmuth F, Kohl Z, Adame A, Trejo M, Schönig K, Zimmermann F, Bauer C, Casadei N, Giel C, Calaminus C, Pichler BJ, Jensen PH, Müller CP, Amato D, Kornhuber J, Teismann P, Yamakado H, Takahashi R, Winkler J, Masliah E, Riess O.

Brain · 2013-02-01

DOI: 10.1093/brain/aws358PMID: 23413261

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Open access

Triggering of inflammasome by aggregated α-synuclein, an inflammatory response in synucleinopathies.

Codolo G, Plotegher N, Pozzobon T, Brucale M, Tessari I, Bubacco L, de Bernard M.

PLoS One · 2013-01-31

DOI: 10.1371/journal.pone.0055375PMID: 23383169

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

15.286 articles found

A case of restless leg syndrome in a family with LRRK2 gene mutation.

Immunotherapy for neurodegenerative diseases: focus on α-synucleinopathies.

Selective expression of α-synuclein-immunoreactivity in vesicular acetylcholine transporter-immunoreactive axons in the guinea pig rectum and human colon.

Alpha-synuclein pathology and axonal degeneration of the peripheral motor nerves innervating pharyngeal muscles in Parkinson disease.

[Genetics of movement disorders].

Mapping the subcellular distribution of α-synuclein in neurons using genetically encoded probes for correlated light and electron microscopy: implications for Parkinson's disease pathogenesis.

RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk.

Parkinson's disease and α-synuclein: passing it on.

APOE ε4 increases risk for dementia in pure synucleinopathies.

C9orf72 repeat expansions are a rare genetic cause of parkinsonism.

A progressive dopaminergic phenotype associated with neurotoxic conversion of α-synuclein in BAC-transgenic rats.

Triggering of inflammasome by aggregated α-synuclein, an inflammatory response in synucleinopathies.

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