- ►nih.gov KK Abu-Amero, TM Bosley - British Journal of Ophthalmology, 2006 - bjo.bmj.com Methods: 19 patients with NAION were compared to 32 controls matched for age,
sex distribution, and ethnicity. DNA was extracted from leucocytes and
competitive multiplex polymerase chain reaction was carried out with two ... Cited by 11 - Related articles - BL Direct - All 6 versions
- ►nih.gov MY Yen, CS Chen, AG Wang, YH Wei - British Journal of Ophthalmology, 2002 - bjo.bmj.com Conclusion: The results suggest that the increase in mtDNA content in LHON
patients with 11778 mtDNA mutation may be due to a compensatory effect for
respiratory chain defects of mitochondria. However, the increase of mtDNA ... Cited by 21 - Related articles - BL Direct - All 8 versions
TM Bosley, CS Constantinescu, CR Tench, … - Mol Vis, 2007 - molvis.org Optic neuritis (ON) is a spontaneous optic neuropathy characterized by
demyelination that can occur in isolation or as part of multiple sclerosis (MS)
[1]. Mitochondria may play a role in MS [2], and mitochondrial ... Cited by 8 - Related articles - View as HTML - All 3 versions
KK Abu-Amero, TM Bosley - British Journal of Ophthalmology, 2007 - bjo.bmj.com Referring to our first report, they stated that “… most of the polymorphisms
found in NAION patients are ancient, well known mtDNA variants defining specific
haplogroups (mtDNA maternal lineages) of European populations.” In fact, ... Cited by 4 - Related articles - All 3 versions
- ►iovs.org [PDF] KK Abu-Amero, TM Bosley - Investigative ophthalmology & visual science, 2006 - ARVO Khaled K. Abu-Amero 1 and Thomas M. Bosley 2,3,4 ... P URPOSE . To investigate
certain biochemical and molecular characteristics of mitochondria in patients
with Leber heredi- tary optic neuropathy (LHON)-like optic neuropathies. M ... Cited by 18 - Related articles - BL Direct - All 5 versions
KK Abu-Amero, TM Bosley - Archives of Pathology and Laboratory Medicine, 2005 - arpa.allenpress.com Archives of Pathology and Laboratory Medicine: Vol. 129, No. 10, pp.
1295–1298. ... Context.—Laboratory methods currently available for
detecting mitochondrial respiratory dysfunction are labor-intensive, ... Cited by 15 - Related articles - BL Direct - All 6 versions
- ►nih.gov AA Sadun, V Carelli - British Medical Journal, 2006 - bjo.bmj.com See end of article for authors' affiliations .......................
Correspondence to: Jean-Louis Pépin, Laboratoire du sommeil, EFCR, CHU de
Grenoble, BP 217X, 38043, Grenoble Cedex 09, France; jpepin@chu- ... Cited by 3 - Related articles - BL Direct - All 6 versions
T Nishioka, A Soemantri, T Ishida - Journal of Human Genetics, 2004 - Springer Abstract Leber's hereditary optic neuropathy (LHON) is a maternally inherited
disease caused by mitochondrial DNA (mtDNA) mutations. In this study, the mtDNA/
nuclear DNA ratio was evaluated in 11 LHON patients with the 14484 ... Cited by 4 - Related articles - All 5 versions
