Mitochondrial analysis in autosomal dominant hereditary spastic paraplegia

Neurology

Volumn 55, Issue 10, 2000, Pages 1591-1592

  Hedera, P ^a   DiMauro, S ^b   Bonilla, E ^b   Wald, J J ^a   Fink, John K ^a,c,d  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b Department of Neurology and the Taub Institute for Research on Alzheimer's Disease and the Aging Brain   (United States)

^c VA ANN ARBOR HEALTHCARE SYSTEM   (United States)

^d Box 0940 ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CITRATE SYNTHASE; CYTOCHROME C OXIDASE; MITOCHONDRIAL ENZYME; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; SUCCINATE DEHYDROGENASE;

ARTICLE; CHROMOSOME 14Q; CHROMOSOME 15Q; CHROMOSOME 2P; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME ACTIVITY; FAMILY STUDY; HEREDITARY MOTOR SENSORY NEUROPATHY; HISTOCHEMISTRY; HUMAN; HUMAN TISSUE; MUSCLE BIOPSY; NERVE FIBER DEGENERATION; PRIORITY JOURNAL;

EID: 0034727613     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.10.1591     Document Type: Article

References (7)

1. Hereditary spastic paraplegia: Genetic heterogeneity and genotype-phenotype correlation
2. Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease
3. Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q
4. Autosomal dominant hereditary spastic paraparesis, type I: Clinical and genetic analysis of a large North American family
5. Cytochemistry and immunocytochemistry of mitochondria on tissue sections
6. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
7. Familial spastic paraparesis. Is it mitochondrial disorder?