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EEG characteristics in juvenile Huntington's disease: a case report and review of the literature.
Epileptic disorders, 2003The clinical features of Juvenile Huntington's Disease (J-HD) differ from those of the more common adult-onset form, and include cognitive decline, parkinsonism, myoclonus and seizures.
M. Landau, K. Cannard
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Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis
Lancet Neurology, 2018C. Fusilli+18 more
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Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington’s disease
Neurology, 1999Martha Nance+4 more
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Onconephrology: The intersections between the kidney and cancer
Ca-A Cancer Journal for Clinicians, 2021Mitchell H Rosner+2 more
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Juvenile Huntington’s Disease: Diagnostic and Treatment Considerations for the Psychiatrist
Current Psychiatry Reports, 2017Joanna Quigley
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Seizures in juvenile Huntington's disease: Frequency and characterization in a multicenter cohort
Movement Disorders, 2012L. Cloud+14 more
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Multidisciplinary standards of care and recent progress in pancreatic ductal adenocarcinoma
Ca-A Cancer Journal for Clinicians, 2020Aaron J Grossberg+2 more
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Juvenile Huntington’s disease presenting as progressive myoclonic epilepsy
Neurology, 2001A. Gambardella+11 more
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