A Huntington's disease phenocopy characterized by pallido-nigro-luysian degeneration with brain iron accumulation and p62-positive glial inclusions

Neuropathology and Applied Neurobiology

Volumn 36, Issue 6, 2010, Pages 551-557

  Ahmed, Z ^a   Tabrizi, S J ^b   Li, A ^a   Houlden, H ^a   Sailer, A ^a   Lees, A J ^a   Revesz, T ^a   Holton, J L ^a  

^a Department of Molecular Neuroscienc ^*  (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; ATAXIN 1; ATAXIN 3; CERULOPLASMIN; COPPER; IRON; MITOCHONDRIAL DNA; PANTOTHENATE KINASE 2; PROTEIN P62;

ACANTHOCYTOSIS; AMYGDALOID NUCLEUS; ARTICLE; ASTROCYTE; BRAIN STEM; CELL NUCLEUS; CEREBELLUM; CEREBROSPINAL FLUID EXAMINATION; CERULOPLASMIN BLOOD LEVEL; DENTATE NUCLEUS; GAZE PARALYSIS; GENE MUTATION; GLIA; GLOBUS PALLIDUS; HIPPOCAMPUS; HUNTINGTON DISEASE LIKE SYNDROME; MICROGLIA; MICROSCOPY; NEUROACANTHOCYTOSIS; NEUROAXONAL DYSTROPHY; NUCLEAR MAGNETIC RESONANCE IMAGING; OLIGODENDROGLIA; PRIORITY JOURNAL; SHY DRAGER SYNDROME; SPINAL CORD; SUBTHALAMIC NUCLEUS; SYPHILIS; VASCULAR AMYLOIDOSIS;

BRAIN; FATAL OUTCOME; HUMANS; HUNTINGTON DISEASE; IMMUNOHISTOCHEMISTRY; INCLUSION BODIES; IRON; MALE; MIDDLE AGED; NERVE DEGENERATION; NEUROGLIA; RNA-BINDING PROTEINS;

EID: 77956534968     PISSN: 03051846     EISSN: 13652990     Source Type: Journal    
DOI: 10.1111/j.1365-2990.2010.01093.x     Document Type: Article

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