Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology

Neuropathology

Volumn 21, Issue 3, 2001, Pages 212-217

  Nomura, Hiroshi ^a   Koike, Fumihiko ^b   Tsuruta, Yuko ^c   Iwaki, Akiko ^d   Iwaki, Toru ^a  

^a Graduate School of Medical Sciences   (Japan)

^b KYUSHU UNIVERSITY   (Japan)

^c Chikugo Municipal Hospital   (Japan)

^d KYUSHU UNIVERSITY   (Japan)

Author keywords

Autosomal recessive inheritance; Complicated form; Cytochrome c oxidase; Hereditary spastic paraplegia; Mitochondria

Indexed keywords

CYTOCHROME C OXIDASE;

ADULT; ARTICLE; ASTROCYTOSIS; AUTOPSY; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DYSARTHRIA; FEMALE; GAIT DISORDER; HUMAN; HUMAN TISSUE; MUSCLE ATROPHY; PNEUMONIA; PRIORITY JOURNAL; SPASTIC PARAPLEGIA;

AUTOPSY; BRAIN; ENZYMES; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; LINKAGE (GENETICS); LIPOFUSCIN; METALLOENDOPEPTIDASES; MIDDLE AGED; MITOCHONDRIAL DISEASES; MUSCLE, SKELETAL; MUSCULAR ATROPHY; NERVE DEGENERATION; NEURONS; PEDIGREE; SPASTIC PARAPLEGIA, HEREDITARY; SPINAL CORD; UBIQUITIN;

EID: 0034773892     PISSN: 09196544     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-1789.2001.00388.x     Document Type: Article

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