CSF1R mutations link POLD and HDLS as a single disease entity-Reference-Cited by-同舟云学术

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CSF1R mutations link POLD and HDLS as a single disease entity

Published:2013-02-13 Issue:11 Volume:80 Page:1033-1040
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Nicholson A. M.,Baker M. C.,Finch N. A.,Rutherford N. J.,Wider C.,Graff-Radford N. R.,Nelson P. T.,Clark H. B.,Wszolek Z. K.,Dickson D. W.,Knopman D. S.,Rademakers R.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 134 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. Deciphering glial contributions to CSF1R-related disorder via single-nuclear transcriptomic profiling: a case study;Acta Neuropathologica Communications;2024-08-28

2. Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Estimation of pathological lesion stage from brain images;Journal of the Neurological Sciences;2024-06

3. An adapted protocol to derive microglia from stem cells and its application in the study of CSF1R-related disorders;Molecular Neurodegeneration;2024-04-05

4. Clinical presentation and diagnosis of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia: a literature analysis of case studies;Frontiers in Neurology;2024-03-11

5. The Phenotypic and Genotypic Spectrum of CSF1R‐Related Disorder in China;Movement Disorders;2024-03-11

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