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Scholar Results 1 - 4 of 4 citing Cohn: The natural history of OPA1-related autosomal dominant optic atrophy. (0.13 sec) 

Inherited mitochondrial optic neuropathies

- nih.gov
P Yu-Wai-Man, PG Griffiths, G Hudson, PF … - British Medical Journal - jmg.bmj.com
Leber hereditary optic neuropathy (LHON) and autosomal dominant optic atrophy
(DOA) are the two most common inherited optic neuropathies and they result in
significant visual morbidity among young adults. Both disorders are the ...
Cited by 3 - Related articles - All 4 versions

Electrodiagnostic assessment in optic nerve disease


GE Holder, RP Gale, JF Acheson, AG Robson - Current opinion in neurology, 2009 - journals.lww.com
Recent findings: The relationship between nerve fibre layer anatomy and the
pattern visual evoked potential has been addressed, correlating axonal loss with
visual pathway dysfunction. Longitudinal assessment of multiple sclerosis ...
Cited by 1 - Related articles - All 3 versions

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders


V Carelli, C La Morgia, ML Valentino, P … - BBA-Bioenergetics, 2009 - Elsevier
Since the early days of mitochondrial medicine, it has been clear that optic
atrophy is a very common and sometimes singular pathological feature in
mitochondrial disorders. The first point mutation of mitochondrial DNA ...
Cited by 1 - Related articles - All 2 versions

Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of …


P Yu-Wai-Man, VJ Davies, MJ Piechota, LM … - Investigative Ophthalmology & Visual Science, 2009 - ARVO
PURPOSE. The majority of patients with autosomal dominant optic atrophy (DOA)
harbor pathogenic OPA1 mutations and certain missense mutations, mostly within
the GTPase domain, have recently been shown to cause multiple mitochondrial ...
Related articles - All 3 versions


 


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