The Golgi apparatus is fragmented in spinal cord motor neurons of amyotrophic lateral sclerosis with basophilic inclusions

Acta Neuropathologica

Volumn 103, Issue 3, 2002, Pages 243-247

  Fujita, Yukio ^a   Okamoto, Koichi ^a   Sakurai, Atsushi ^a   Kusaka, Hirofumi ^b   Aizawa, Hitoshi ^c   Mihara, Ban ^d   Gonatas, Nicholas K ^e  

^a GUNMA UNIVERSITY   (Japan)

^b KANSAI MEDICAL UNIVERSITY   (Japan)

^c ASAHIKAWA MEDICAL COLLEGE   (Japan)

^d Institute of Brain and Blood VesselsMihara Memorial Hospital   (Japan)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Amyotrophic lateral sclerosis; Anterior horn cell; Basophilic inclusion; Golgi apparatus; MG160

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL CELL; ARTICLE; BASOPHIL; CASE REPORT; CELL AGGREGATION; CELL FUNCTION; CELL INCLUSION; CONTROLLED STUDY; CYTOPLASM; FAMILIAL DISEASE; FEMALE; FRAGMENTATION REACTION; GENE EXPRESSION; GENE MUTATION; GOLGI COMPLEX; HUMAN; HUMAN CELL; HUMAN TISSUE; MOUSE; NERVE CELL DEGENERATION; NERVE CELL LESION; NERVE CELL NECROSIS; NEUROPATHOLOGY; NONHUMAN; PARALYSIS; PATHOGENESIS; PRIORITY JOURNAL; SPINAL CORD MOTONEURON; TRANSGENIC MOUSE;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ANTERIOR HORN CELLS; BASOPHILS; DNA FRAGMENTATION; FEMALE; GOLGI APPARATUS; HUMANS; INCLUSION BODIES; MALE; MIDDLE AGED; MOTOR NEURONS; MUTATION; SPINAL CORD; SUPEROXIDE DISMUTASE;

EID: 0036943001     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010100461     Document Type: Article

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