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A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea.

Salpietro V, Perez-Dueñas B, Nakashima K, San Antonio-Arce V, Manole A, Efthymiou S, Vandrovcova J, Bettencourt C, Mencacci NE, Klein C, Kelly MP, Davies CH, Kimura H, Macaya A, Houlden H.

Mov Disord · 2018-02-02

DOI: 10.1002/mds.27286PMID: 29392776

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Alpha galactosidase A activity in Parkinson's disease.

Alcalay RN, Wolf P, Levy OA, Kang UJ, Waters C, Fahn S, Ford B, Kuo SH, Vanegas N, Shah H, Liong C, Narayan S, Pauciulo MW, Nichols WC, Gan-Or Z, Rouleau GA, Chung WK, Oliva P, Keutzer J, Marder K, Zhang XK.

Neurobiol Dis · 2018-02-02

DOI: 10.1016/j.nbd.2018.01.012PMID: 29369793

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

Subthalamic deep brain stimulation under general anesthesia and neurophysiological guidance while on dopaminergic medication: comparative cohort study.

Asha MJ, Fisher B, Kausar J, Garratt H, Krovvidi H, Shirley C, White A, Chelvarajah R, Ughratdar I, Hodson JA, Pall H, Mitchell RD.

Acta Neurochir (Wien) · 2018-02-02

DOI: 10.1007/s00701-018-3473-4PMID: 29396602

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

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