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Quoted phrase not found in phrase index: "Hereditary spastic paraplegia 29"
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MEP recruitment curves in multiple sclerosis and hereditary spastic paraplegia.
J Neurol Sci. 2005 Oct 15;237(1-2):25-9. doi: 10.1016/j.jns.2005.05.002.
J Neurol Sci. 2005.
PMID: 15961111
Clinical Trial.
Multiple sclerosis (MS) represents both demyelination and axonal degeneration. Hereditary Spastic Paraplegia (HSP) was included as a model of pure axonal loss. ...The MEP-recruitment curves were obtained by means of transcranial magnetic stimulation (TMS) in …
Multiple sclerosis (MS) represents both demyelination and axonal degeneration. Hereditary Spastic Paraplegia (HSP) was …
Improving gait adaptability in patients with hereditary spastic paraplegia (Move-HSP): study protocol for a randomized controlled trial.
van de Venis L, van de Warrenburg BPC, Weerdesteyn V, van Lith BJH, Geurts ACH, Nonnekes J.
van de Venis L, et al.
Trials. 2021 Jan 7;22(1):32. doi: 10.1186/s13063-020-04932-9.
Trials. 2021.
PMID: 33413555
Free PMC article.
BACKGROUND: People with hereditary spastic paraplegia (HSP) experience difficulties adapting their gait to meet environmental demands, a skill required for safe and independent ambulation. ...In addition, this study aims to identify key determinants of C-Mill …
BACKGROUND: People with hereditary spastic paraplegia (HSP) experience difficulties adapting their gait to meet environ …
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Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic.
Hamanaka K, Miyatake S, Zerem A, Lev D, Blumkin L, Yokochi K, Fujita A, Imagawa E, Iwama K, Nakashima M, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Saitsu H, van der Knaap MS, Lerman-Sagie T, Matsumoto N.
Hamanaka K, et al.
J Hum Genet. 2018 Dec;63(12):1223-1229. doi: 10.1038/s10038-018-0516-x. Epub 2018 Sep 27.
J Hum Genet. 2018.
PMID: 30258207
Clinical Trial.
Biallelic mutations in IBA57 cause a mitochondrial disorder with a broad phenotypic spectrum that ranges from severe intellectual disability to adolescent-onset spastic paraplegia. Only 21 IBA57 mutations have been reported, therefore the phenotypic spectrum of IBA5 …
Biallelic mutations in IBA57 cause a mitochondrial disorder with a broad phenotypic spectrum that ranges from severe intellectual disability …
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