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Volumn 5, Issue 6, 2001, Pages 225-242

Xeroderma pigmentosum/Cockayne syndrome complex: First neuropathological study and review of eight other cases

Author keywords

Cachexia; Deficient DNA repair; Growth failure; Neuropathology; Premature aging; Xeroderma pigmentosum Cockayne syndrome complex

Indexed keywords

ATAXIA; BRAIN GROWTH; BRAIN WEIGHT; CACHEXIA; CALCINOSIS; CASE REPORT; CATARACT; CELL NUCLEUS; CHILD; CHILDHOOD DISEASE; CILIARY BODY; COCKAYNE SYNDROME; CONTROLLED STUDY; DEMYELINATING DISEASE; ENDOTHELIUM CELL; EYE DISEASE; FACIES; GENOTYPE; GLIA CELL; GLIOSIS; GROWTH DISORDER; HEARING LOSS; HUMAN; HUMAN TISSUE; HYDROCEPHALUS; INFANCY; IRIS ATROPHY; MALE; MYOPATHY; NERVE FIBER DEGENERATION; NEUROMUSCULAR DISEASE; NEUROPATHOLOGY; OPTIC NERVE ATROPHY; PATHOPHYSIOLOGY; PERIPHERAL NERVE; PERIPHERAL NEUROPATHY; PHENOTYPE; PIGMENT DISORDER; POSTNATAL GROWTH; PRIORITY JOURNAL; RETINA DISEASE; RETINA PIGMENT EPITHELIOPATHY; RETINOPATHY; REVIEW; SKELETAL MUSCLE; SKIN SENSITIVITY; SPASTICITY; SUN EXPOSURE; XERODERMA PIGMENTOSUM;

EID: 0035164519     PISSN: 10903798     EISSN: None     Source Type: Journal    
DOI: 10.1053/ejpn.2001.0523     Document Type: Review
Times cited : (70)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.