Ondine's curse in a woman with Leber's hereditary optic neuropathy [6]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 73, Issue 3, 2002, Pages 347-348

  Sadler, M ^a   Wiles, C M ^a   Stoodley, N ^a   Linnane, S J ^a   Smith, A P ^a  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; CASE REPORT; CLINICAL FEATURE; FEMALE; GLASGOW COMA SCALE; HEREDITARY OPTIC ATROPHY; HUMAN; LETTER; MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; POSITIVE END EXPIRATORY PRESSURE; PRIORITY JOURNAL;

ADULT; BRAIN; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; OPTIC ATROPHY, HEREDITARY, LEBER; POINT MUTATION; SLEEP APNEA, CENTRAL;

EID: 0036724851     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.73.3.347     Document Type: Letter

References (5)

1. Occurrence of a multiple sclerosis like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
2. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
3. Brainstem involvement in Leber's hereditary optic neuropathy: Association with the 14484 mitochondrial DNA mutation
4. Automatic respiratory failure associated with infarction in the medulla
5. Sleep apnea following percutaneous cervical cordotomy