Hereditary spastic paraplegia caused by the PLP1 'rumpshaker mutation'-Reference-Cited by-同舟云学术

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Hereditary spastic paraplegia caused by the PLP1 'rumpshaker mutation'

Published:2009-12-01 Issue:6 Volume:81 Page:666-672
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Svenstrup K.,Giraud G.,Boespflug-Tanguy O.,Danielsen E. R.,Thomsen C.,Rasmussen K.,Law I.,Vogel A.,Stokholm J.,Crone C.,Hjermind L. E.,Nielsen J. E.

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Metabolite profile in hereditary spastic paraplegia analyzed using magnetic resonance spectroscopy: a cross-sectional analysis in a longitudinal study;Frontiers in Neuroscience;2024-08-13

2. Neuroimaging in hereditary spastic paraplegias: from qualitative cues to precision biomarkers;Expert Review of Molecular Diagnostics;2022-07-03

3. Frontotemporal Pathology in Motor Neuron Disease Phenotypes: Insights From Neuroimaging;Frontiers in Neurology;2021-08-16

4. Hypomyelinating leukodystrophies — unravelling myelin biology;Nature Reviews Neurology;2020-12-15

5. Brain Magnetic Spectroscopy Imaging and Hereditary Spastic Paraplegia: A Focused Systematic Review on Current Landmarks and Future Perspectives;Frontiers in Neurology;2020-07-14

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