The otolaryngological manifestations of mitochondrial disease and the risk of neurodegeneration with infection

Archives of Otolaryngology - Head and Neck Surgery

Volumn 128, Issue 4, 2002, Pages 355-362

  Edmonds, Joseph L ^a,f   Kirse, Daniel J ^b   Kearns, Donald ^a   Deutsch, Reena ^c   Spruijt, Liesbeth ^d,g   Naviaux, Robert K ^e,h  

^a RADY CHILDREN'S HOSPITAL   (United States)

^b UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^e UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^f Texas Children's Hospital   (United States)

^g MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^h UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BIOENERGY; BRAIN STEM; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONDUCTION DEAFNESS; DEVELOPMENT; DISORDERS OF MITOCHONDRIAL FUNCTIONS; HEARING LOSS; HIGH RISK POPULATION; HUMAN; INFANT; INFECTION; INTERVIEW; NERVE DEGENERATION; NEWBORN; OTORHINOLARYNGOLOGY; RECURRENT INFECTION; RISK ASSESSMENT; UPPER RESPIRATORY TRACT INFECTION;

EID: 0036216401     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.128.4.355     Document Type: Article

References (23)

1. Organismal effects of mitochondrial dysfunction
2. Mitochondrial DNA disorders
3. The mitochondrial DNA depletion syndromes
4. Mitochondrial encephalomyelopathies
5. Protean manifestations of mitochondrial diseases: A minireview
6. Clinical presentations and laboratory investigations in respiratory chain deficiency
7. Genetic causes of hearing loss
8. Mitochondrial genetics and hearing loss: The missing link between genotype and phenotype
9. Mitochondrial deafness
10. Auditory brainstem response from children three months to three years of age: Normal patterns of response II
11. The Seattle Virus Watch, II: Objectives, study, population and observation, data processing, and summary of illnesses
12. Reye's syndrome
13. Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation
14. Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides
15. Cochlear origin of hearing loss in MELAS syndrome
16. Abnormal evoked potentials of Kearns-Sayre syndrome
17. Electrophysiological brainstem dysfunction in a child with Leigh disease
18. Auditory brainstem response in Leigh's syndrome
19. Evoked potentials in children with oxidative metabolic defects leading to Leigh syndrome
20. Mitochondrial genetics and hearing loss: The missing link between genotype and phenotype
21. Mitochondrial defects and hearing loss
22. Non-mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss
23. Anesthesia and mitochondrial cytopathies