Neurodegeneration in hereditary nucleotide repair disorders

Brain and Development

Volumn 21, Issue 5, 1999, Pages 326-333

  Itoh, Masahiro ^a,b   Hayashi, Masaharu ^a   Shioda, Kei ^c   Minagawa, Masao ^c   Isa, Fumiko ^d   Tamagawa, Kimiko ^e   Morimatsu, Yoshio ^a   Oda, Masaya ^e  

^a Tokyo Metropolitan Institute   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^c SAITAMA MEDICAL UNIVERSITY   (Japan)

^d Tokyo Metropolitan Kita Medical and Rehabilitation Center   (Japan)

^e TOKYO METROPOLITAN NEUROLOGICAL HOSPITAL   (Japan)

Author keywords

Calcification; Cockayne syndrome; Demyelination; Grumose or foamy spheroid body; Neuronal loss; Neuropathology; Nucleotide repair; Xeroderma pigmentosum

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOPSY; AUTOSOMAL DISORDER; BASAL GANGLION; CEREBELLUM CORTEX; CLINICAL ARTICLE; CLINICAL TRIAL; COCKAYNE SYNDROME; DNA DAMAGE; DNA REPAIR; FEMALE; GLOBUS PALLIDUS; HUMAN; LOCUS CERULEUS; MALE; MORPHOMETRICS; NERVE DEGENERATION; NEUROFIBRILLARY TANGLE; NEUROPATHOLOGY; OLIVARY NUCLEUS; SUBSTANTIA NIGRA; XERODERMA PIGMENTOSUM;

ADOLESCENT; ADULT; AXONS; CEREBRAL CORTEX; CHILD; COCKAYNE SYNDROME; DNA REPAIR; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; NERVE FIBERS, MYELINATED; NEURONS; NEUROPIL; XERODERMA PIGMENTOSUM;

EID: 0033026499     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(99)00033-9     Document Type: Article

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