- ►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
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
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
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