Almost complete spontaneous recovery in visual function was observed in a male patient with Leber's hereditary optic neuropathy (LHON), in spite of the presence of several LHON-associated major" and minor" mutations of mitochondrial DNA. Our findings confirm that visual loss in LHON may be reversible, and challenge the hypothesis of a synergistic" effect of multiple mtDNA mutations in the phenotypic expression of the disease. © 1994 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted
Leber Hereditary Optic Neuropathy (LHON) is one of the most common mitochondrial diseases that can c...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...
The predominant manifestation of Leber hereditary optic neuropathy (LHON) is a sudden and usually se...
In 3 young male patients, aged 10, 19 and 21 years respectively, sequential, severe, painless bilate...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder that causes severe los...
Leber hereditary optic neuropathy (LHON) is a maternally inherited bilaterally blinding optic neurop...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
AbstractLeber’s hereditary optic neuropathy (LHON) has traditionally been considered a disease causi...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
Item does not contain fulltextIn 3 young male patients, aged 10, 19 and 21 years respectively, seque...
The elucidation of approximately one dozen mtDNA mutations has renewed interest in Leber's hereditar...
The onset of Leber hereditary optic neuropathy is relatively rare in childhood and, interestingly, t...
Leber Hereditary Optic Neuropathy (LHON) is one of the most common mitochondrial diseases that can c...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...
The predominant manifestation of Leber hereditary optic neuropathy (LHON) is a sudden and usually se...
In 3 young male patients, aged 10, 19 and 21 years respectively, sequential, severe, painless bilate...
Leber's hereditary optic neuropathy (LHON) is a maternally inherited disorder that causes severe los...
Leber hereditary optic neuropathy (LHON) is a maternally inherited bilaterally blinding optic neurop...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
AbstractLeber’s hereditary optic neuropathy (LHON) has traditionally been considered a disease causi...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
Leber hereditary optic neuropathy (LHON) is a maternally inherited disorder, associated with mutatio...
Item does not contain fulltextIn 3 young male patients, aged 10, 19 and 21 years respectively, seque...
The elucidation of approximately one dozen mtDNA mutations has renewed interest in Leber's hereditar...
The onset of Leber hereditary optic neuropathy is relatively rare in childhood and, interestingly, t...
Leber Hereditary Optic Neuropathy (LHON) is one of the most common mitochondrial diseases that can c...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...
Four new missense mutations have been identified through restriction analysis and sequencing of the ...