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Volumn 5, Issue 6, 2001, Pages 225-242
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Xeroderma pigmentosum/Cockayne syndrome complex: First neuropathological study and review of eight other cases
a,b a,c a d d a,e |
Author keywords
Cachexia; Deficient DNA repair; Growth failure; Neuropathology; Premature aging; Xeroderma pigmentosum Cockayne syndrome complex
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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;
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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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References (63)
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