Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): A single entity?

Neurology

Volumn 72, Issue 22, 2009, Pages 1953-1959

  Wider, C ^a   Van Gerpen, J A ^a   Dearmond, S ^b   Shuster, E A ^a   Dickson, D W ^a   Wszolek, Z K ^a  

^a MAYO CLINIC   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE NUCLEOTIDE EXCHANGE FACTOR; LAMIN B; PROTEIN LAMIN B1; UNCLASSIFIED DRUG;

BEHAVIOR CHANGE; BRAIN BIOPSY; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DEMENTIA; DEPRESSION; EPILEPSY; FAMILIAL PIGMENTARY ORTHOCHROMATIC LEUKODYSTROPHY; GAIT DISORDER; GENE MUTATION; GENETIC DISORDER; HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY WITH AXONAL SPHEROID; HUMAN; LEUKODYSTROPHY; LEUKOENCEPHALOPATHY; MOTOR DYSFUNCTION; MYELIN SHEATH; NERVE FIBER DEGENERATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PEDIGREE; PRIORITY JOURNAL; PYRAMIDAL TRACT; REVIEW; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; TUMOR SPHEROID;

EID: 67650066957     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181a826c0     Document Type: Review

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