Studies on Leber's optic neuropathy III
- 1 January 1989
- journal article
- research article
- Published by Springer Nature in Documenta Ophthalmologica
- Vol. 71 (1) , 77-92
- https://doi.org/10.1007/bf00155135
Abstract
Neurological investigations, HLA-typing and viral antibody studies were performed in patients with Leber's optic neuropathy (LON), in individuals at risk to develop the disease, in obligatory (female) carriers of the disease, and compared with controls. The only relevant findings were an excess of minor neurological abnormalities in patients with LON and in some individuals from the at risk group. Occasionally, an association of LON and a multiple sclerosis-like picture was observed.This publication has 30 references indexed in Scilit:
- LEBER'S HEREDITARY OPTIC NEURORETINOPATHY: A MITOCHONDRIAL DISEASE?Acta Neurologica Scandinavica, 1984
- Thiosulfat-sulfur-transferase-Mangel bei Lebers hereditärer OptikusatrophieKlinische Monatsblätter für Augenheilkunde, 1982
- Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.Journal of Medical Genetics, 1977
- LEBER'S DISEASE VActa Ophthalmologica, 1970
- LEBER's DISEASE IIIActa Ophthalmologica, 1969
- LEBER'S DISEASE IIActa Ophthalmologica, 1968
- LEBER'S DISEASEActa Ophthalmologica, 1968
- A FAMILY WITH HEREDITARY SPASTIC ATAXIAActa Neurologica Scandinavica, 1965
- A Sex-linked Heredo-degenerative Neurological Disorder Associated with Leber’s Optic Atrophy Genetical AspectsHuman Heredity, 1964
- THE INHERITANCE OF LEBER'S DISEASE: (CYTOPLASMIC INHERITANCE)Acta Ophthalmologica, 1944