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Navigating the Uncommon: “Juvenile-Onset Huntington Disease”

Journal of Child Neurology
Progressive neurodegeneration with the movement disorder can be challenging to diagnose. In this article, we present a 12-year-old female child with stroke and progressive neurocognitive decline that was followed by choreo-athetoid movements and worsening dystonia and epilepsy.
Anmol Aatli   +4 more
openaire   +2 more sources

Juvenile Huntington's disease.

Neurology India
A rare case of juvenile Huntington's disease manifesting since the age of seven years is reported. The inheritance was typically autosomal dominant as three other members on the paternal side died of similar disease. A definite family history can becrucial in the diagnosis of juvenile Huntington's disease.
C, Pani   +3 more
openaire   +1 more source

Juvenile Huntington Disease

2017
Jaeson Kaylegian, Scott J. Hunter
openaire   +2 more sources

Juvenile Huntington Disease

2011
Scott J. Hunter, Christina Casnar
openaire   +1 more source

Juvenile Huntington's disease

Clinical Neurology and Neurosurgery, 1985
openaire   +1 more source

Juvenile Huntington’s disease: neuropathology

2009
Jean Paul G. Vonsattel   +2 more
openaire   +1 more source

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