PubMed (Bookshelf cited) for id: 375157

Year	Number of Results
2003	1
2009	1
2010	2
2012	2
2014	2
2015	2
2016	3
2017	3
2018	2
2019	1
2020	7
2021	6
2024	0

1

Pathophysiology and Treatment of Non-motor Dysfunction in Amyotrophic Lateral Sclerosis.

Mahoney CJ, Ahmed RM, Huynh W, Tu S, Rohrer JD, Bedlack RS, Hardiman O, Kiernan MC. Mahoney CJ, et al. CNS Drugs. 2021 May;35(5):483-505. doi: 10.1007/s40263-021-00820-1. Epub 2021 May 15. CNS Drugs. 2021. PMID: 33993457 Review.

2

DCTN1 Binds to TDP-43 and Regulates TDP-43 Aggregation.

Deshimaru M, Kinoshita-Kawada M, Kubota K, Watanabe T, Tanaka Y, Hirano S, Ishidate F, Hiramoto M, Ishikawa M, Uehara Y, Okano H, Hirose S, Fujioka S, Iwasaki K, Yuasa-Kawada J, Mishima T, Tsuboi Y. Deshimaru M, et al. Int J Mol Sci. 2021 Apr 13;22(8):3985. doi: 10.3390/ijms22083985. Int J Mol Sci. 2021. PMID: 33924373 Free PMC article.

3

Perry syndrome with progressive supranuclear palsy-like phenotype in a Portuguese family - Long-term clinical follow-up.

Barreto RD, Rodrigues R, Roriz JM, Alonso I, Magalhães M. Barreto RD, et al. Parkinsonism Relat Disord. 2021 Mar;84:74-76. doi: 10.1016/j.parkreldis.2021.02.004. Epub 2021 Feb 5. Parkinsonism Relat Disord. 2021. PMID: 33578072 No abstract available.

4

Meta-iodobenzylguanidine myocardial scintigraphy in Perry disease.

Mishima T, Fujioka S, Nishioka K, Li Y, Sato K, Houzen H, Yabe I, Shiomi K, Eriguchi M, Hara H, Hattori N, Tsuboi Y. Mishima T, et al. Parkinsonism Relat Disord. 2021 Feb;83:49-53. doi: 10.1016/j.parkreldis.2020.12.017. Epub 2021 Jan 12. Parkinsonism Relat Disord. 2021. PMID: 33476877

5

A novel Q93H missense mutation in DCTN1 caused distal hereditary motor neuropathy type 7B and Perry syndrome from a Chinese family.

Zhang J, Wang H, Liu W, Wang J, Zhang J, Chang X, Huang S, Pang X, Guo J, Wang Q, Zhang W. Zhang J, et al. Neurol Sci. 2021 Sep;42(9):3695-3705. doi: 10.1007/s10072-020-04962-w. Epub 2021 Jan 14. Neurol Sci. 2021. PMID: 33443672

6

Perry Disease: Concept of a New Disease and Clinical Diagnostic Criteria.

Tsuboi Y, Mishima T, Fujioka S. Tsuboi Y, et al. J Mov Disord. 2021 Jan;14(1):1-9. doi: 10.14802/jmd.20060. Epub 2020 Sep 21. J Mov Disord. 2021. PMID: 32942840 Free PMC article.

7

Cognitive and behavioral profile of Perry syndrome in two families.

Milanowski Ł, Sitek EJ, Dulski J, Cerquera-Cleves C, Gomez JD, Brockhuis B, Schinwelski M, Kluj-Kozłowska K, Ross OA, Sławek J, Wszolek ZK. Milanowski Ł, et al. Parkinsonism Relat Disord. 2020 Aug;77:114-120. doi: 10.1016/j.parkreldis.2020.05.019. Epub 2020 Jun 22. Parkinsonism Relat Disord. 2020. PMID: 32717578

8

The Human Gene Mutation Database (HGMD^®): optimizing its use in a clinical diagnostic or research setting.

Stenson PD, Mort M, Ball EV, Chapman M, Evans K, Azevedo L, Hayden M, Heywood S, Millar DS, Phillips AD, Cooper DN. Stenson PD, et al. Hum Genet. 2020 Oct;139(10):1197-1207. doi: 10.1007/s00439-020-02199-3. Epub 2020 Jun 28. Hum Genet. 2020. PMID: 32596782 Free PMC article. Review.

9

Amyotrophic lateral sclerosis: a clinical review.

Masrori P, Van Damme P. Masrori P, et al. Eur J Neurol. 2020 Oct;27(10):1918-1929. doi: 10.1111/ene.14393. Epub 2020 Jul 7. Eur J Neurol. 2020. PMID: 32526057 Free PMC article. Review.

10

Progressive supranuclear palsy: Advances in diagnosis and management.

Coughlin DG, Litvan I. Coughlin DG, et al. Parkinsonism Relat Disord. 2020 Apr;73:105-116. doi: 10.1016/j.parkreldis.2020.04.014. Epub 2020 May 25. Parkinsonism Relat Disord. 2020. PMID: 32487421 Free PMC article. Review.

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