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Thermoregulatory and metabolic defects in Huntington''s disease transgenic mice implicate PGC-1alpha in Huntington''s disease neurodegeneration.Academic Article Why?
A variation of Capgras syndrome with anosognosia in Huntington''s disease: a case report.Academic Article Why?
Increased TRPC5 glutathionylation contributes to striatal neuron loss in Huntington''s disease.Academic Article Why?
Neuroanatomical Visualization of the Impaired Striatal Connectivity in Huntington''s Disease Mouse Model.Academic Article Why?
The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington''s disease patients.Academic Article Why?
Identification of Genetic Factors that Modify Clinical Onset of Huntington''s Disease.Academic Article Why?
A modifier of Huntington''s disease onset at the MLH1 locus.Academic Article Why?
A systems-level "misunderstanding": the plasma metabolome in Huntington''s disease.Academic Article Why?
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington''s disease motor onset.Academic Article Why?
Haplotype-based stratification of Huntington''s disease.Academic Article Why?
Safety and tolerability of high-dosage coenzyme Q10 in Huntington''s disease and healthy subjects.Academic Article Why?
Study of plasma-derived miRNAs mimic differences in Huntington''s disease brain.Academic Article Why?
Epigenetic mechanisms of neurodegeneration in Huntington''s disease.Academic Article Why?
MicroRNAs located in the Hox gene clusters are implicated in huntington''s disease pathogenesis.Academic Article Why?
Nucleolar dysfunction in Huntington''s disease.Academic Article Why?
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