PRE-EXCITATION SYNDROME AND LEBER'S HEREDITARY OPTIC NEURORETINOPATHY

The Lancet

Volumn 325, Issue 8430, 1985, Pages 696-

  Nikoskelainen, E ^a   Wanne, O ^a   Dahl, M ^a  

^a UNIVERSITY OF TURKU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL INHERITANCE; BLINDNESS; CENTRAL NERVOUS SYSTEM; CLINICAL ARTICLE; DIAGNOSIS; ELECTROCARDIOGRAPHY; ETIOLOGY; HEART; HEART PREEXCITATION; HEREDITY; HUMAN; LEBER CONGENITAL AMAUROSIS; PRIORITY JOURNAL; VISUAL SYSTEM; WOLFF PARKINSON WHITE SYNDROME;

FEMALE; GENETIC DISEASES, INBORN; HUMAN; MALE; OPTIC NERVE DISEASES; RETINAL DISEASES; WOLFF-PARKINSON-WHITE SYNDROME;

EID: 0021913432     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(85)91354-6     Document Type: Letter

References (9)

1. Preexcitation syndrome
2. Familial Wolff-Parkinson-White syndrome
3. Mechanisms and diagnosis of arrhythmias
4. Mitochondrial inheritance in a mitochondrially mediated disease
5. Fundus findings in Leber's hereditary optic neuroretinopathy III: Fluorescein angiographic studies
6. Leber's hereditary optic atrophy: Some clinical and aetiological considerations
7. The heart in Leber's optic atrophy
8. Familial occurrence of Wolff-Parkinson-White syndrome
9. Leber's hereditary optic neuroretinopathy, a mitochondrial disease