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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1949 2
1950 2
1951 1
1953 4
1954 3
1955 1
1956 2
1957 1
1958 3
1959 3
1960 2
1962 3
1963 5
1964 4
1967 1
1968 1
1969 4
1970 2
1971 3
1972 4
1973 7
1974 4
1975 13
1976 8
1977 14
1978 11
1979 16
1980 21
1981 21
1982 23
1983 42
1984 36
1985 60
1986 38
1987 63
1988 85
1989 103
1990 114
1991 115
1992 143
1993 251
1994 218
1995 265
1996 231
1997 244
1998 274
1999 255
2000 298
2001 299
2002 255
2003 184
2004 199
2005 214
2006 225
2007 222
2008 232
2009 215
2010 224
2011 228
2012 271
2013 260
2014 270
2015 268
2016 298
2017 303
2018 283
2019 358
2020 343
2021 331
2022 313
2023 284
2024 114

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8,528 results

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Page 1
Mitochondrial neuropathy and neurogenic features in mitochondrial myopathy.
Lu JQ, Tarnopolsky MA. Lu JQ, et al. Mitochondrion. 2021 Jan;56:52-61. doi: 10.1016/j.mito.2020.11.005. Epub 2020 Nov 19. Mitochondrion. 2021. PMID: 33220502 Review.
Mitochondrial diseases (MIDs) involve multiple organs including peripheral nerves and skeletal muscle. Mitochondrial neuropathy (MN) and mitochondrial myopathy (MM) are commonly associated and linked at the neuromuscular junction (NMJ). ...
Mitochondrial diseases (MIDs) involve multiple organs including peripheral nerves and skeletal muscle. Mitochondrial neuropath
Mitochondrial myopathy diagnosis.
Shoffner JM. Shoffner JM. Neurol Clin. 2000 Feb;18(1):105-23. doi: 10.1016/s0733-8619(05)70180-8. Neurol Clin. 2000. PMID: 10658170 Review.
Niacin Cures Systemic NAD(+) Deficiency and Improves Muscle Performance in Adult-Onset Mitochondrial Myopathy.
Pirinen E, Auranen M, Khan NA, Brilhante V, Urho N, Pessia A, Hakkarainen A, Kuula J, Heinonen U, Schmidt MS, Haimilahti K, Piirilä P, Lundbom N, Taskinen MR, Brenner C, Velagapudi V, Pietiläinen KH, Suomalainen A. Pirinen E, et al. Cell Metab. 2020 Jun 2;31(6):1078-1090.e5. doi: 10.1016/j.cmet.2020.04.008. Epub 2020 May 7. Cell Metab. 2020. PMID: 32386566 Free article.
Here, we report systemic NAD(+) deficiency in adult-onset mitochondrial myopathy patients. We administered an increasing dose of NAD(+)-booster niacin, a vitamin B3 form (to 750-1,000 mg/day; clinicaltrials.govNCT03973203) for patients and their matched controls for …
Here, we report systemic NAD(+) deficiency in adult-onset mitochondrial myopathy patients. We administered an increasing dose …
Diagnosis and Treatment of Mitochondrial Myopathies.
Ahmed ST, Craven L, Russell OM, Turnbull DM, Vincent AE. Ahmed ST, et al. Neurotherapeutics. 2018 Oct;15(4):943-953. doi: 10.1007/s13311-018-00674-4. Neurotherapeutics. 2018. PMID: 30406383 Free PMC article. Review.
Mitochondrial myopathies are progressive muscle conditions caused primarily by the impairment of oxidative phosphorylation (OXPHOS) in the mitochondria. ...Moreover, recent developments in the reproductive options for patients with mitochondrial myopathies
Mitochondrial myopathies are progressive muscle conditions caused primarily by the impairment of oxidative phosphorylation (OX
Chronic kidney disease and acquired mitochondrial myopathy.
Rao M, Jaber BL, Balakrishnan VS. Rao M, et al. Curr Opin Nephrol Hypertens. 2018 Mar;27(2):113-120. doi: 10.1097/MNH.0000000000000393. Curr Opin Nephrol Hypertens. 2018. PMID: 29266014 Review.
PURPOSE OF REVIEW: Sarcopenia and muscle weakness contribute to fragility and limit exercise tolerance among patients with CKD. This review focuses on the role of reduction in mitochondrial mass and function in the myopathy associated with CKD, causes for these musc …
PURPOSE OF REVIEW: Sarcopenia and muscle weakness contribute to fragility and limit exercise tolerance among patients with CKD. This review …
Interactions of mitochondrial and skeletal muscle biology in mitochondrial myopathy.
Di Leo V, Bernardino Gomes TM, Vincent AE. Di Leo V, et al. Biochem J. 2023 Nov 15;480(21):1767-1789. doi: 10.1042/BCJ20220233. Biochem J. 2023. PMID: 37965929 Free PMC article. Review.
Furthermore, interactions between mitochondrial dysfunction and skeletal muscle biology, in mitochondrial myopathy, likely have important implications for normal muscle function and physiology. In this review, we will try to give an overview of what is known …
Furthermore, interactions between mitochondrial dysfunction and skeletal muscle biology, in mitochondrial myopathy, lik …
The Spectrum of Mitochondrial Ultrastructural Defects in Mitochondrial Myopathy.
Vincent AE, Ng YS, White K, Davey T, Mannella C, Falkous G, Feeney C, Schaefer AM, McFarland R, Gorman GS, Taylor RW, Turnbull DM, Picard M. Vincent AE, et al. Sci Rep. 2016 Aug 10;6:30610. doi: 10.1038/srep30610. Sci Rep. 2016. PMID: 27506553 Free PMC article. Review.
Characterizing abnormal mitochondrial structural features may thus provide insight into the underlying pathogenesis of inherited and acquired mitochondrial diseases. Following a systematic literature review on ultrastructural defects in mitochondrial myopa
Characterizing abnormal mitochondrial structural features may thus provide insight into the underlying pathogenesis of inherited and …
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort.
Montano V, Lopriore P, Gruosso F, Carelli V, Comi GP, Filosto M, Lamperti C, Mongini T, Musumeci O, Servidei S, Tonin P, Toscano A, Primiano G, Valentino ML, Bortolani S, Marchet S, Ricci G, Modenese A, Cotti Piccinelli S, Risi B, Meneri M, Arena IG, Siciliano G, Mancuso M. Montano V, et al. J Neurol. 2022 Dec;269(12):6555-6565. doi: 10.1007/s00415-022-11324-3. Epub 2022 Aug 18. J Neurol. 2022. PMID: 35980466 Free PMC article.
OBJECTIVES: To assess natural history and 12-month change of a series of scales and functional outcome measures in a cohort of 117 patients with primary mitochondrial myopathy (PMM). METHODS: Twelve months follow-up data of 117 patients with PMM were collected. ...P …
OBJECTIVES: To assess natural history and 12-month change of a series of scales and functional outcome measures in a cohort of 117 patients …
Primary mitochondrial myopathies in childhood.
Olimpio C, Tiet MY, Horvath R. Olimpio C, et al. Neuromuscul Disord. 2021 Oct;31(10):978-987. doi: 10.1016/j.nmd.2021.08.005. Neuromuscul Disord. 2021. PMID: 34736635 Review.
Primary mitochondrial myopathies are genetic metabolic disorders of mitochondrial dysfunction affecting mainly, but not exclusively, skeletal muscle. ...Mitochondrial myopathy in infants presents with hypotonia, muscle weakness and difficulty fe …
Primary mitochondrial myopathies are genetic metabolic disorders of mitochondrial dysfunction affecting mainly, but not …
Mitochondrial myopathy: a rare cause of early-onset vocal fold atrophy.
Kelly EA, Bock JM, Peltier AC, Oh SJ, Garrett CG. Kelly EA, et al. Ann Otol Rhinol Laryngol. 2013 Mar;122(3):177-82. doi: 10.1177/000348941312200306. Ann Otol Rhinol Laryngol. 2013. PMID: 23577570 Free PMC article. Review.
OBJECTIVES: We present the second published case of laryngeal involvement in mitochondrial myopathy. METHODS: A patient with laryngeal involvement of mitochondrial myopathy is presented, together with a literature review. RESULTS: A 41-year-old man pre …
OBJECTIVES: We present the second published case of laryngeal involvement in mitochondrial myopathy. METHODS: A patient with l …
8,528 results