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Neurocase
Behavior, Cognition and Neuroscience
Volume 22, 2016 - Issue 3
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Review

A young-onset frontal dementia with dramatic calcifications due to a novel CSF1R mutation

Ethan GoreDepartment of Neurology, Case Western Reserve University Hospitals, Beachwood, OH, USACorrespondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-3279-2191
ORCID Icon,
Andrew ManleyDepartment of Neurology, University of South Alabama, Mobile, AL, USA
,
Daniel DeesDepartment of Neurology, University of South Alabama, Mobile, AL, USA
,
Brian S. ApplebyDepartment of Neurology, Case Western Reserve University Hospitals, Beachwood, OH, USA
&
Alan J. LernerDepartment of Neurology, Case Western Reserve University Hospitals, Beachwood, OH, USA
Pages 257-262 | Received 11 Sep 2015, Accepted 23 Mar 2016, Published online: 19 Apr 2016

Citations (10)

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Read on this site (2)

Jie Chen, Shiying Luo, Ning Li, Huimin Li, Jinming Han & Li Ling. (2020) A Novel Missense Mutation of the CSF1R Gene Causes Incurable CSF1R-Related Leukoencephalopathy: Case Report and Review of Literature. International Journal of General Medicine 13, pages 1613-1620.
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Rishi Sharma, Jonathan Graff-Radford, Rosa Rademakers, Bradley F. Boeve, Ronald C. Petersen & David T. Jones. (2019) CSF1R mutation presenting as dementia with Lewy bodies. Neurocase 25:1-2, pages 17-20.
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Articles from other publishers (8)

Violeta Chitu, Şölen Gökhan & E. Richard Stanley. (2021) Modeling CSF‐1 receptor deficiency diseases – how close are we?. The FEBS Journal 289:17, pages 5049-5073.
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Goda‐Camille Mickeviciute, Monika Valiuskyte, Michael Plattén, Zbigniew K. Wszolek, Oluf Andersen, Virginija Danylaité Karrenbauer, Benjamin V. Ineichen & Tobias Granberg. (2021) Neuroimaging phenotypes of CSF1R ‐related leukoencephalopathy: Systematic review, meta‐analysis, and imaging recommendations . Journal of Internal Medicine 291:3, pages 269-282.
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Hiu Chuen Lok & John B. Kwok. (2021) The Role of White Matter Dysfunction and Leukoencephalopathy/Leukodystrophy Genes in the Aetiology of Frontotemporal Dementias: Implications for Novel Approaches to Therapeutics. International Journal of Molecular Sciences 22:5, pages 2541.
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Daniel W. Sirkis, Ethan G. Geier, Luke W. Bonham, Celeste M. Karch & Jennifer S. Yokoyama. (2019) Recent Advances in the Genetics of Frontotemporal Dementia. Current Genetic Medicine Reports 7:1, pages 41-52.
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Seong-Ik Kim, Beomseok Jeon, Jeongmo Bae, Jae Kyung Won, Han-Joon Kim, Jeemin Yim, Yun Joong Kim & Sung-Hye Park. (2019) An Autopsy Proven Case of CSF1R-mutant Adult-onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) with Premature Ovarian Failure. Experimental Neurobiology 28:1, pages 119-129.
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Takuya KonnoKoji KasanukiTakeshi IkeuchiDennis W. DicksonZbigniew K. Wszolek. (2018) CSF1R -related leukoencephalopathy . Neurology 91:24, pages 1092-1104.
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Scott J. Adams, Andrew Kirk & Roland N. Auer. (2018) Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Integrating the literature on hereditary diffuse leukoencephalopathy with spheroids (HDLS) and pigmentary orthochromatic leukodystrophy (POLD). Journal of Clinical Neuroscience 48, pages 42-49.
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Kensuke Daida, Kenya Nishioka, Yuanzhe Li, Sho Nakajima, Ryota Tanaka & Nobutaka Hattori. (2017) <i>CSF1R</i> Mutation p.G589R and the Distribution Pattern of Brain Calcification. Internal Medicine 56:18, pages 2507-2512.
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