Hematologic Follow-up as Clue to Polycythemia Vera due to JAK2 Mutation Presenting as Late Onset Chorea
Author:
Affiliation:
1. Department of Neurology; University Medical Center Hamburg-Eppendorf; Hamburg Germany
2. Department of Neurology; Ludwig-Maximilians-University; Munich Germany
Funder
German Parkinson Society
Else Kröner-Fresenius-Stiftung
Deutsche Forschungsgemeinschaft
VolkswagenStiftung
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mdc3.12548/fullpdf
Reference10 articles.
1. The causes of sporadic and ‘senile’ chorea;Warren;Aust N Z J Med,1998
2. Therapeutic recommendations in polycythemia vera based on Polycythemia Vera Study Group protocols;Berk;Semin Hematol,1986
3. Diagnosis and classification of the polycythemias;Berlin;Semin Hematol,1975
4. Chronic myeloproliferative diseases;Lacerda;Handb Clin Neurol,2014
5. Chorea in the elderly with mutation positive polycythemia vera: a case report;Kumar;Can J Neurol Sci,2009
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2. Neuropsychiatric disturbance detecting polycythemia vera myelofibrosis: a case report and literature review;Frontiers in Neurology;2023-09-22
3. Neurologic Manifestations of Systemic Disease: Movement Disorders;Current Treatment Options in Neurology;2021-01
4. Aceruloplasminemia Presenting with Asymmetric Chorea Due to a Novel Frameshift Mutation;Movement Disorders Clinical Practice;2020-09
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