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Items: 8

1.

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.

Kurian MA, Zhen J, Cheng SY, Li Y, Mordekar SR, Jardine P, Morgan NV, Meyer E, Tee L, Pasha S, Wassmer E, Heales SJ, Gissen P, Reith ME, Maher ER.

J Clin Invest. 2009 Jun;119(6):1595-603. doi: 10.1172/JCI39060.

2.

ADHD and the dopamine transporter: are there reasons to pay attention?

Mazei-Robinson MS, Blakely RD.

Handb Exp Pharmacol. 2006;(175):373-415. Review.

PMID:
16722244
3.

Rare causes of dystonia parkinsonism.

Schneider SA, Bhatia KP.

Curr Neurol Neurosci Rep. 2010 Nov;10(6):431-9. doi: 10.1007/s11910-010-0136-0. Review.

PMID:
20694531
4.

Human genetics and pharmacology of neurotransmitter transporters.

Lin Z, Madras BK.

Handb Exp Pharmacol. 2006;(175):327-71. Review.

PMID:
16722243
5.

Dopamine transporter imaging as a diagnostic tool for parkinsonism and related disorders in clinical practice.

Ba F, Martin WR.

Parkinsonism Relat Disord. 2015 Feb;21(2):87-94. doi: 10.1016/j.parkreldis.2014.11.007. Review.

PMID:
25487733
6.

Dystonia-plus syndromes.

Asmus F, Gasser T.

Eur J Neurol. 2010 Jul;17 Suppl 1:37-45. doi: 10.1111/j.1468-1331.2010.03049.x. Review.

PMID:
20590807
7.
8.

The natural history of sex-linked recessive dystonia parkinsonism of Panay, Philippines (XDP).

Lee LV, Maranon E, Demaisip C, Peralta O, Borres-Icasiano R, Arancillo J, Rivera C, Munoz E, Tan K, Reyes MT.

Parkinsonism Relat Disord. 2002 Oct;9(1):29-38. Review.

PMID:
12217620
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