Letter to the Editor
Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation

https://doi.org/10.1016/j.parkreldis.2010.05.001Get rights and content

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Cited by (7)

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    PGRN mutations are suggested to be one of the most common causes of familial CBS [29]. Parkinsonism seen in FTDP-17 (PGRN) cases may initially respond to levodopa; however, in most cases, it is not levodopa-sensitive [37,38]. The specific PGRN mutations in which parkinsonism are most likely to be observed are summarized in Table 4.

  • Clinical Guidelines for Cognitive Disorders in Elderly and Older Patients

    2021, Zhurnal Nevrologii i Psihiatrii imeni S.S. Korsakova
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The review of this paper was entirely handled by the Co-Editor-in-Chief, Ronald Pfeiffer.

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