Ataxic presentation of progressive multifocal leukoencephalopathy: an uncommon phenotype
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s13760-022-02049-1.pdf
Reference5 articles.
1. Koralnik IJ, Schellingerhout D, Frosch MP (2004) Case records of the Massachusetts General Hospital Weekly clinicopathological exercises Case 14–2004 A 66- year-old man with progressive neurologic deficits. N Engl J Med 350:1882–93. https://doi.org/10.1056/NEJMcpc030038
2. Kastrup O, Wanke I, Esser S, Maschke M (2005) Evolution of purely infratentorial PML under HAART-negative outcome under rapid immune reconstitution. Clin Neurol Neurosurg 107:509–513
3. Cinque P, Koralnik IJ, Gerevini S et al (2009) Progressive multifocal leukoencephalopathy in HIV-1 infection. Lancet Infect Dis 9(10):625–636. https://doi.org/10.1016/S1473-3099(09)70226-9
4. Garrels K, Kucharczyk W, Wortzman G et al (1996) Progressive multifocal leukoencephalopathy: clinical and MR response to treatment. AJNR Am J Neuroradiol 17(3):597–600
5. Fontoura P, Vale J, Lima C, Scaravilli F, Guimarães J (2002) Progressive myoclonic ataxia and JC virus encephalitis in an AIDS patient. J Neurol Neurosurg Psychiatr 72(5):653–656
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