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keywords > Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System
Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability.
Dysfunctional astrocytes as key players in the pathogenesis of central nervous system disorders.
Gene-targeted therapies for the central nervous system.
Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiency.
Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.
Depletion of mitochondrial DNA in leukocytes of patients with poly-Q diseases.
Differential production of superoxide by neuronal mitochondria.
CAG repeat disorder models and human neuropathology: similarities and differences.
Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems.
MRI and SPECT of midbrain and striatal degeneration in fragile X-associated tremor/ataxia syndrome.