Autosomal recessive spastic paraplegia with hypoplastic corpus callosum, multisystem degeneration and ubiquitinated eosinophilic granules

Acta Neuropathologica

Volumn 101, Issue 1, 2001, Pages 69-73

  Wakabayashi, Koichi ^a   Kobayashi, Hisashi ^b   Kawasaki, Sari ^b   Kondo, Hiroshi ^b   Takahashi, Hitoshi ^a  

^a NIIGATA UNIVERSITY   (Japan)

^b National Hospital Organization Niigata National Hospital   (Japan)

Author keywords

Corpus callosum; Familial spastic paraplegia; Hypoplasia; Lipofuscin; Substantia nigra

Indexed keywords

LIPOFUSCIN; MELANIN; UBIQUITIN;

ADULT; AGE; ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE DISORDER; BRAIN DEVELOPMENT; CASE REPORT; CELL INCLUSION; CLINICAL FEATURE; CORPUS CALLOSUM; DEGENERATIVE DISEASE; DENTATE NUCLEUS; DISEASE SEVERITY; FAMILY; FEMALE; GLIOSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; LATERAL GENICULATE BODY; MENTAL DEFICIENCY; MOTONEURON; MUSCLE ATROPHY; MYELINATION; NERVE CELL; PARENT; PIGMENTATION; PRIORITY JOURNAL; SENSORY DYSFUNCTION; SIBLING; SPINAL CORD; SUBSTANTIA NIGRA; THALAMUS; THICKNESS;

CENTRAL NERVOUS SYSTEM; CORPUS CALLOSUM; CYTOPLASMIC GRANULES; DISEASE PROGRESSION; EOSINE YELLOWISH-(YS); FEMALE; HUMANS; MIDDLE AGED; NERVE DEGENERATION; NEURONS; SPASTIC PARAPLEGIA, HEREDITARY; UBIQUITINS;

EID: 0035144658     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010000255     Document Type: Article

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