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Results: 18

1.

DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypes.

Caroppo P, Le Ber I, Clot F, Rivaud-Péchoux S, Camuzat A, De Septenville A, Boutoleau-Bretonnière C, Mourlon V, Sauvée M, Lebouvier T, Bonnet AM, Levy R, Vercelletto M, Brice A; French Clinical and Genetic Research Network on Frontotemporal Dementia/Frontotemporal Dementia–Amyotrophic Lateral Sclerosis.

JAMA Neurol. 2014 Feb;71(2):208-15. doi: 10.1001/jamaneurol.2013.5100.

PMID:
24343258
[PubMed - indexed for MEDLINE]
2.

Dynactin subunit p150(Glued) is a neuron-specific anti-catastrophe factor.

Lazarus JE, Moughamian AJ, Tokito MK, Holzbaur EL.

PLoS Biol. 2013 Jul;11(7):e1001611. doi: 10.1371/journal.pbio.1001611. Epub 2013 Jul 16.

PMID:
23874158
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Perry syndrome: a disorder to consider in the differential diagnosis of Parkinsonism.

Aji BM, Medley G, O'Driscoll K, Larner AJ, Alusi SH.

J Neurol Sci. 2013 Jul 15;330(1-2):117-8. doi: 10.1016/j.jns.2013.04.008. Epub 2013 Apr 28.

PMID:
23628468
[PubMed - indexed for MEDLINE]
4.

Cytoplasmic dynein in neurodegeneration.

Eschbach J, Dupuis L.

Pharmacol Ther. 2011 Jun;130(3):348-63. doi: 10.1016/j.pharmthera.2011.03.004. Epub 2011 Mar 21. Review.

PMID:
21420428
[PubMed - indexed for MEDLINE]
5.

Autonomic failures in Perry syndrome with DCTN1 mutation.

Ohshima S, Tsuboi Y, Yamamoto A, Kawakami M, Farrer MJ, Kira J, Shii H.

Parkinsonism Relat Disord. 2010 Nov;16(9):612-4. doi: 10.1016/j.parkreldis.2010.07.001. Epub 2010 Aug 11.

PMID:
20702129
[PubMed - indexed for MEDLINE]
6.

Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure.

Newsway V, Fish M, Rohrer JD, Majounie E, Williams N, Hack M, Warren JD, Morris HR.

Mov Disord. 2010 Apr 30;25(6):767-70. doi: 10.1002/mds.22950.

PMID:
20437543
[PubMed - indexed for MEDLINE]
7.

Elucidating the genetics and pathology of Perry syndrome.

Wider C, Dachsel JC, Farrer MJ, Dickson DW, Tsuboi Y, Wszolek ZK.

J Neurol Sci. 2010 Feb 15;289(1-2):149-54. doi: 10.1016/j.jns.2009.08.044. Epub 2009 Sep 4.

PMID:
19732908
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Characterization of DCTN1 genetic variability in neurodegeneration.

Vilariño-Güell C, Wider C, Soto-Ortolaza AI, Cobb SA, Kachergus JM, Keeling BH, Dachsel JC, Hulihan MM, Dickson DW, Wszolek ZK, Uitti RJ, Graff-Radford NR, Boeve BF, Josephs KA, Miller B, Boylan KB, Gwinn K, Adler CH, Aasly JO, Hentati F, Destée A, Krygowska-Wajs A, Chartier-Harlin MC, Ross OA, Rademakers R, Farrer MJ.

Neurology. 2009 Jun 9;72(23):2024-8. doi: 10.1212/WNL.0b013e3181a92c4c.

PMID:
19506225
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Transcranial sonography in Perry syndrome.

Saka E, Topcuoglu MA, Demir AU, Elibol B.

Parkinsonism Relat Disord. 2010 Jan;16(1):68-70. doi: 10.1016/j.parkreldis.2009.05.010. Epub 2009 Jun 7.

PMID:
19505837
[PubMed - indexed for MEDLINE]
10.

DCTN1 mutations in Perry syndrome.

Farrer MJ, Hulihan MM, Kachergus JM, Dächsel JC, Stoessl AJ, Grantier LL, Calne S, Calne DB, Lechevalier B, Chapon F, Tsuboi Y, Yamada T, Gutmann L, Elibol B, Bhatia KP, Wider C, Vilariño-Güell C, Ross OA, Brown LA, Castanedes-Casey M, Dickson DW, Wszolek ZK.

Nat Genet. 2009 Feb;41(2):163-5. doi: 10.1038/ng.293. Epub 2009 Jan 11.

PMID:
19136952
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Pallidonigral TDP-43 pathology in Perry syndrome.

Wider C, Dickson DW, Stoessl AJ, Tsuboi Y, Chapon F, Gutmann L, Lechevalier B, Calne DB, Personett DA, Hulihan M, Kachergus J, Rademakers R, Baker MC, Grantier LL, Sujith OK, Brown L, Calne S, Farrer MJ, Wszolek ZK.

Parkinsonism Relat Disord. 2009 May;15(4):281-6. doi: 10.1016/j.parkreldis.2008.07.005. Epub 2008 Aug 23.

PMID:
18723384
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome)--a literature review.

Wider C, Wszolek ZK.

Parkinsonism Relat Disord. 2008;14(1):1-7. Epub 2007 Sep 17. Review.

PMID:
17870652
[PubMed - indexed for MEDLINE]
13.

Neurodegeneration involving putative respiratory neurons in Perry syndrome.

Tsuboi Y, Dickson DW, Nabeshima K, Schmeichel AM, Wszolek ZK, Yamada T, Benarroch EE.

Acta Neuropathol. 2008 Feb;115(2):263-8. Epub 2007 Jun 19.

PMID:
17576579
[PubMed - indexed for MEDLINE]
14.

Japanese family with parkinsonism, depression, weight loss, and central hypoventilation.

Tsuboi Y, Wszolek ZK, Kusuhara T, Doh-ura K, Yamada T.

Neurology. 2002 Apr 9;58(7):1025-30.

PMID:
11940687
[PubMed - indexed for MEDLINE]
15.

Familial parkinsonism with depression: a clinicopathological study.

Bhatia KP, Daniel SE, Marsden CD.

Ann Neurol. 1993 Dec;34(6):842-7.

PMID:
8250534
[PubMed - indexed for MEDLINE]
16.

Familial parkinsonism, apathy, weight loss, and central hypoventilation: successful long-term management.

Roy EP 3rd, Riggs JE, Martin JD, Ringel RA, Gutmann L.

Neurology. 1988 Apr;38(4):637-9.

PMID:
3352925
[PubMed - indexed for MEDLINE]
17.

Localized cicatricial pemphigoid (Brunsting-Perry syndrome).

Gibson V, Tschen JA, Bean SF.

Cutis. 1986 Oct;38(4):252-3.

PMID:
3536333
[PubMed - indexed for MEDLINE]
18.

Familial fatal Parkinsonism with alveolar hypoventilation and mental depression.

Purdy A, Hahn A, Barnett HJ, Bratty P, Ahmad D, Lloyd KG, McGeer EG, Perry TL.

Ann Neurol. 1979 Dec;6(6):523-31.

PMID:
43704
[PubMed - indexed for MEDLINE]

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