Reid E - Search Results

1

Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.

Shribman S, Reid E, Crosby AH, Houlden H, Warner TT. Shribman S, et al. Among authors: reid e. Lancet Neurol. 2019 Dec;18(12):1136-1146. doi: 10.1016/S1474-4422(19)30235-2. Epub 2019 Jul 31. Lancet Neurol. 2019. PMID: 31377012 Review.

2

Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project.

Bourinaris T, Smedley D, Cipriani V, Sheikh I, Athanasiou-Fragkouli A, Chinnery P, Morris H, Real R, Harrison V, Reid E, Wood N; Genomics England Research Consortium; Vandrovcova J, Houlden H, Tucci A. Bourinaris T, et al. Among authors: reid e. Eur J Hum Genet. 2020 Dec;28(12):1763-1768. doi: 10.1038/s41431-020-00720-w. Epub 2020 Sep 15. Eur J Hum Genet. 2020. PMID: 32934340 Free PMC article.

3

Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.

Proukakis C, Auer-Grumbach M, Wagner K, Wilkinson PA, Reid E, Patton MA, Warner TT, Crosby AH. Proukakis C, et al. Among authors: reid e. Hum Mutat. 2003 Feb;21(2):170. doi: 10.1002/humu.9108. Hum Mutat. 2003. PMID: 12552568

4

Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype.

Smith BN, Bevan S, Vance C, Renwick P, Wilkinson P, Proukakis C, Squitieri F, Berardelli A, Warner TT, Reid E, Shaw CE. Smith BN, et al. Among authors: reid e. Clin Genet. 2009 May;75(5):485-9. doi: 10.1111/j.1399-0004.2009.01184.x. Clin Genet. 2009. PMID: 19459885

5

Diagnosis, investigation and management of hereditary spastic paraplegias in the era of next-generation sequencing.

Hensiek A, Kirker S, Reid E. Hensiek A, et al. Among authors: reid e. J Neurol. 2015 Jul;262(7):1601-12. doi: 10.1007/s00415-014-7598-y. Epub 2014 Dec 6. J Neurol. 2015. PMID: 25480570 Free PMC article.

6

Many pathways lead to hereditary spastic paraplegia.

Reid E. Reid E. Lancet Neurol. 2003 Apr;2(4):210. doi: 10.1016/s1474-4422(03)00345-4. Lancet Neurol. 2003. PMID: 12849205 No abstract available.

7

X-linked adrenoleukodystrophy presenting as autosomal dominant pure hereditary spastic paraparesis.

Shaw-Smith CJ, Lewis SJ, Reid E. Shaw-Smith CJ, et al. Among authors: reid e. J Neurol Neurosurg Psychiatry. 2004 May;75(5):686-8. doi: 10.1136/jnnp.2003.022970. J Neurol Neurosurg Psychiatry. 2004. PMID: 15090559 Free PMC article.

8

The hereditary spastic paraplegias.

Reid E. Reid E. J Neurol. 1999 Nov;246(11):995-1003. doi: 10.1007/s004150050503. J Neurol. 1999. PMID: 10631629 Review.

9

The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the effect of disease mutations on WASH complex assembly and function.

Freeman C, Seaman MN, Reid E. Freeman C, et al. Among authors: reid e. Biochim Biophys Acta. 2013 Jan;1832(1):160-73. doi: 10.1016/j.bbadis.2012.10.011. Epub 2012 Oct 23. Biochim Biophys Acta. 2013. PMID: 23085491 Free PMC article.

10

Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia.

Newton T, Allison R, Edgar JR, Lumb JH, Rodger CE, Manna PT, Rizo T, Kohl Z, Nygren AOH, Arning L, Schüle R, Depienne C, Goldberg L, Frahm C, Stevanin G, Durr A, Schöls L, Winner B, Beetz C, Reid E. Newton T, et al. Among authors: reid e. Brain. 2018 May 1;141(5):1286-1299. doi: 10.1093/brain/awy034. Brain. 2018. PMID: 29481671 Free PMC article.

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