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Cited by 26

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Clinical and demographic features of chronic progressive external ophthalmoplegia in a large adult-onset cohort

Heighton, Julia N., Brady, Lauren I., Newman, Matthew C., Tarnopolsky, Mark A.·2019·Mitochondrion

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Citations

Cites

Research works printed but not linked: 35

  1. Arden, 1997, Genetic influences on muscle strength, lean body mass, and bone mineral density: a twin study, J. Bone Miner. Res., 12, 2076, 10.1359/jbmr.1997.12.12.2076 · DOI · Paper page
  2. Brady, 2014, Impact of habitual exercise on the strength of individuals with myotonic dystrophy type 1, Am. J. Phys. Med. Rehabil., 93, 739, 10.1097/PHM.0000000000000088 · DOI
  3. Cruz, 2017, Clinical, biochemical, molecular and histological features of 65 Portuguese patients with mitochondrial disorders, Muscle Nerve, 56, 868, 10.1002/mus.25593 · DOI
  4. Danta, 1975, Chronic progressive external ophthalmoplegia, Brain, 98, 473, 10.1093/brain/98.3.473 · DOI
  5. Dimitriadis, 2014, Leber's hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients, Orphanet. J. Rare Dis., 9, 10.1186/s13023-014-0158-9 · DOI
  6. Dougherty, 2001, Metabolic testing in mitochondrial disease, Semin. Neurol., 21, 303, 10.1055/s-2001-17947 · DOI
  7. Giordano, 2011, Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy, Brain, 134, 220, 10.1093/brain/awq276 · DOI · Paper page
  8. Hanisch, 2015, SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions, J. Neurol. Neurosurg. Psychiatry, 86, 630, 10.1136/jnnp-2013-306748 · DOI
  9. Hedermann, 2017, Dysphagia is prevalent in patients with CPEO and single, large-scale deletions in mtDNA, Mitochondrion, 32, 27, 10.1016/j.mito.2016.11.007 · DOI
  10. Hudson, 2007, Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background, Am. J. Hum. Genet., 81, 228, 10.1086/519394 · DOI · Paper page
  11. Indo, 2007, Evidence of ROS generation by mitochondria in cells with impaired electron transport chain and mitochondrial DNA damage, Mitochondrion, 7, 106, 10.1016/j.mito.2006.11.026 · DOI · Paper page
  12. Jou, 2005, Enhanced generation of mitochondrial reactive oxygen species in cybrids containing 4977-bp mitochondrial DNA deletion, Ann. N. Y. Acad. Sci., 1042, 221, 10.1196/annals.1338.024 · DOI
  13. Kirkman, 2009, Gene-environment interactions in Leber hereditary optic neuropathy, Brain, 132, 2317, 10.1093/brain/awp158 · DOI · Paper page
  14. Kiyomoto, 2006, Frequency of dystrophic muscle abnormalities in chronic progressive external ophthalmoplegia: analysis of 86 patients, J. Neurol. Neurosurg. Psychiatry, 77, 541, 10.1136/jnnp.2005.079954 · DOI
  15. Kojima, 2015, Lifestyle-related factors contributing to decline in knee extension strength among elderly women: a cross-sectional and longitudinal cohort study, PLoS One, 10, e0132523, 10.1371/journal.pone.0132523 · DOI
  16. Kok, 2012, The longitudinal relation between smoking and muscle strength in healthy adults, Eur. Addict. Res., 18, 70, 10.1159/000333600 · DOI
  17. Kornblum, 2005, Sensorineural hearing loss in patients with chronic progressive external ophthalmoplegia or Kearns-Sayre syndrome, J. Neurol., 252, 1101, 10.1007/s00415-005-0827-7 · DOI
  18. Leonard, 2000, Mitochondrial respiratory chain disorders I: mitochondrial DNA defects, Lancet, 355, 299, 10.1016/S0140-6736(99)05225-3 · DOI · Paper page
  19. Lin, 2012, Mouse mtDNA mutant model of Leber hereditary optic neuropathy, Proc. Natl. Acad. Sci. U. S. A., 109, 20065, 10.1073/pnas.1217113109 · DOI · Paper page
  20. Miró, 1999, Smoking disturbs mitochondrial respiratory chain function and enhances lipid peroxidation on human circulating lymphocytes, Carcinogenesis, 20, 1331, 10.1093/carcin/20.7.1331 · DOI
  21. Montes de Oca, 2008, Peripheral muscle alterations in non-COPD smokers, Chest, 133, 13, 10.1378/chest.07-1592 · DOI
  22. Nelson, 1994, Smoking, alcohol, and neuromuscular and physical function of older women. Study of osteoporotic fractures research group, JAMA, 272, 1825, 10.1001/jama.1994.03520230035035 · DOI
  23. Paramasivam, 2016, Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging, Mitochondrion, 26, 81, 10.1016/j.mito.2015.12.006 · DOI
  24. Pfeffer, 2013, Diagnosis and treatment of mitochondrial myopathies, Ann. Med., 45, 4, 10.3109/07853890.2011.605389 · DOI
  25. Pfeffer, 2011, Multisystem disorder in late-onset chronic progressive external ophthalmoplegia, Can. J. Neurol. Sci., 38, 119, 10.1017/S031716710001115X · DOI
  26. Pfeffer, 2014, Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance, Brain, 137, 1323, 10.1093/brain/awu060 · DOI
  27. Puomila, 2007, Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland, Eur. J. Hum. Genet., 15, 1079, 10.1038/sj.ejhg.5201828 · DOI
  28. Sadun, 2011, Leber's hereditary optic neuropathy, Curr. Treat. Options Neurol., 13, 109, 10.1007/s11940-010-0100-y · DOI
  29. Sciacco, 2001, Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation, J. Neurol., 248, 778, 10.1007/s004150170094 · DOI
  30. Smith, 1993, Smoking and mitochondrial function: a model for environmental toxins, Q. J. Med., 86, 657, 10.1093/qjmed/86.10.657 · DOI
  31. Spruijt, 2006, Influence of mutation type on clinical expression of Leber hereditary optic neuropathy, Am J. Ophthalmol., 141, 676, 10.1016/j.ajo.2005.11.007 · DOI
  32. Tarnopolsky, 2011, Suction-modified Bergström muscle biopsy technique: experience with 13,500 procedures, Muscle Nerve, 43, 717, 10.1002/mus.21945 · DOI
  33. Wei, 2001, Increases of mitochondrial mass and mitochondrial genome in association with enhanced oxidative stress in human cells harboring 4977 BP-deleted mitochondrial DNA, Ann. N. Y. Acad. Sci., 928, 97, 10.1111/j.1749-6632.2001.tb05640.x · DOI
  34. Yu-Wai-Man, 2003, The epidemiology of Leber hereditary optic neuropathy in the North East of England, Am. J. Hum. Genet., 72, 333, 10.1086/346066 · DOI · Paper page
  35. Yu-Wai-Man, 2014, A national epidemiological study of chronic progressive external ophthalmoplegia in the United Kingdom - molecular genetic features and neurological burden, Invest. Ophthalmol. Vis. Sci., 55, 5109

Cited by

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Metadata

Authors
Heighton, J. N., Brady, L. I., Newman, M. C., & Tarnopolsky, M. A.
Venue
Mitochondrion
Publisher
Elsevier BV
Published
2019-01
Volume
44
Pages
15-19
ISSN
1567-7249
Cited by
26
References
3
Language
en
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

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