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A de novo loss-of-function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa.

Szczałuba K, Szymańska K, Rydzanicz M, Ciara E, Walczak A, Piekutowska-Abramczuk D, Kosińska J, Jacoszek A, Czerska K, Biernacka A, Laure-Kamionowska M, Gasperowicz P, Pronicka E, Płoski R.

Clin Genet · 2017-12-15

DOI: 10.1111/cge.13133PMID: 29243232

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Protocol of a single group prospective observational study on the diagnostic value of 3T susceptibility weighted MRI of nigrosome-1 in patients with parkinsonian symptoms: the N3<i>i</i>PD study (nigrosomal <b>i</b>ron <b>i</b>maging <b>i</b>n Parkinson's disease).

Schwarz ST, Xing Y, Naidu S, Birchall J, Skelly R, Perkins A, Evans J, Sare G, Martin-Bastida A, Bajaj N, Gowland P, Piccini P, Auer DP.

BMJ Open · 2017-12-14

DOI: 10.1136/bmjopen-2017-016904PMID: 29247084

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Sex disparities in health and health care utilization after Parkinson diagnosis: Rethinking PD associated disability.

Fullard ME, Thibault DP, Todaro V, Foster S, Katz L, Morgan R, Kern DS, Schwalb JM, Urrea Mendoza E, Dahodwala N, Shulman L, Willis AW.

Parkinsonism Relat Disord · 2017-12-14

DOI: 10.1016/j.parkreldis.2017.12.012PMID: 29273434

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

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