-
1
-
-
0027715698
-
Morphological analyses of paraspinal muscles: comparison of progressive lumbar kyphosis (camptocormia) and narrowing of lumbar canal by disc protrusions
-
Delisle MB, Laroche M, Dupont H, Rochaix P, Rumeau JL. Morphological analyses of paraspinal muscles: comparison of progressive lumbar kyphosis (camptocormia) and narrowing of lumbar canal by disc protrusions. Neuromuscul Disord 1993; 3: 579-82.
-
(1993)
Neuromuscul Disord
, vol.3
, pp. 579-582
-
-
Delisle, M.B.1
Laroche, M.2
Dupont, H.3
Rochaix, P.4
Rumeau, J.L.5
-
2
-
-
0037964141
-
Severe forward flexion of the trunk in Parkinson's disease: focal myopathy of the paraspinal muscles mimicking camptocormia
-
Schabitz WR, Glatz K, Schuhan C, Sommer C, Berger C, Schwaninger M, Hartmann M, Hilmar Goebel H, Meinck HM. Severe forward flexion of the trunk in Parkinson's disease: focal myopathy of the paraspinal muscles mimicking camptocormia. Mov Disord 2003; 18: 408-14.
-
(2003)
Mov Disord
, vol.18
, pp. 408-414
-
-
Schabitz, W.R.1
Glatz, K.2
Schuhan, C.3
Sommer, C.4
Berger, C.5
Schwaninger, M.6
Hartmann, M.7
Hilmar Goebel, H.8
Meinck, H.M.9
-
3
-
-
34548620526
-
Axial myopathies: an elderly disorder
-
Serratrice G. Axial myopathies: an elderly disorder. Acta Myol 2007; 26: 11-13.
-
(2007)
Acta Myol
, vol.26
, pp. 11-13
-
-
Serratrice, G.1
-
6
-
-
0029034916
-
Inclusion body myositis presenting with isolated erector spinae paresis
-
Hund E, Heckl R, Goebel HH, Meinck HM. Inclusion body myositis presenting with isolated erector spinae paresis. Neurology 1995; 45: 993-4.
-
(1995)
Neurology
, vol.45
, pp. 993-994
-
-
Hund, E.1
Heckl, R.2
Goebel, H.H.3
Meinck, H.M.4
-
7
-
-
79958155953
-
A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy
-
Sakiyama Y, Okamoto Y, Higuchi I, Inamori Y, Sangatsuda Y, Michizono K, Watanabe O, Hatakeyama H, Goto Y, Arimura K, Takashima H. A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy. Acta Neuropathol (Berl) 2011; 121: 775-83.
-
(2011)
Acta Neuropathol (Berl)
, vol.121
, pp. 775-783
-
-
Sakiyama, Y.1
Okamoto, Y.2
Higuchi, I.3
Inamori, Y.4
Sangatsuda, Y.5
Michizono, K.6
Watanabe, O.7
Hatakeyama, H.8
Goto, Y.9
Arimura, K.10
Takashima, H.11
-
8
-
-
34250155668
-
Myasthenia gravis with concomitant severe paraspinal muscle degeneration and mitochondrial DNA4977 deletion
-
Wakata N, Konno S, Nomoto N, Sugimoto H, Nemoto H, Kurihara T, Kishi M. Myasthenia gravis with concomitant severe paraspinal muscle degeneration and mitochondrial DNA4977 deletion. Intern Med 2007; 46: 747-50.
-
(2007)
Intern Med
, vol.46
, pp. 747-750
-
-
Wakata, N.1
Konno, S.2
Nomoto, N.3
Sugimoto, H.4
Nemoto, H.5
Kurihara, T.6
Kishi, M.7
-
9
-
-
0035887054
-
Ultrastructural changes in paravertebral muscles associated with degenerative spondylolisthesis
-
discussion 5
-
Ramsbacher J, Theallier-Janko A, Stoltenburg-Didinger G, Brock M. Ultrastructural changes in paravertebral muscles associated with degenerative spondylolisthesis. Spine (Phila Pa 1976) 2001; 26: 2180-4; discussion 5.
-
(2001)
Spine (Phila Pa 1976)
, vol.26
, pp. 2180-2184
-
-
Ramsbacher, J.1
Theallier-Janko, A.2
Stoltenburg-Didinger, G.3
Brock, M.4
-
11
-
-
77953627194
-
Somatic mitochondrial DNA mutations in mammalian aging
-
Larsson NG. Somatic mitochondrial DNA mutations in mammalian aging. Annu Rev Biochem 2010; 79: 683-706.
-
(2010)
Annu Rev Biochem
, vol.79
, pp. 683-706
-
-
Larsson, N.G.1
-
12
-
-
77955888547
-
Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO
-
Greaves LC, Yu-Wai-Man P, Blakely EL, Krishnan KJ, Beadle NE, Kerin J, Barron MJ, Griffiths PG, Dickinson AJ, Turnbull DM, Taylor RW. Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO. Invest Ophthalmol Vis Sci 2010; 51: 3340-6.
-
(2010)
Invest Ophthalmol Vis Sci
, vol.51
, pp. 3340-3346
-
-
Greaves, L.C.1
Yu-Wai-Man, P.2
Blakely, E.L.3
Krishnan, K.J.4
Beadle, N.E.5
Kerin, J.6
Barron, M.J.7
Griffiths, P.G.8
Dickinson, A.J.9
Turnbull, D.M.10
Taylor, R.W.11
-
13
-
-
0031885843
-
Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle
-
Brierley EJ, Johnson MA, Lightowlers RN, James OF, Turnbull DM. Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle. Ann Neurol 1998; 43: 217-23.
-
(1998)
Ann Neurol
, vol.43
, pp. 217-223
-
-
Brierley, E.J.1
Johnson, M.A.2
Lightowlers, R.N.3
James, O.F.4
Turnbull, D.M.5
-
14
-
-
33748643416
-
Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers
-
Bua E, Johnson J, Herbst A, Delong B, McKenzie D, Salamat S, Aiken JM. Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers. Am J Hum Genet 2006; 79: 469-80.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 469-480
-
-
Bua, E.1
Johnson, J.2
Herbst, A.3
Delong, B.4
McKenzie, D.5
Salamat, S.6
Aiken, J.M.7
-
15
-
-
0036258718
-
Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function
-
Fayet G, Jansson M, Sternberg D, Moslemi AR, Blondy P, Lombes A, Fardeau M, Oldfors A. Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function. Neuromuscul Disord 2002; 12: 484-93.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 484-493
-
-
Fayet, G.1
Jansson, M.2
Sternberg, D.3
Moslemi, A.R.4
Blondy, P.5
Lombes, A.6
Fardeau, M.7
Oldfors, A.8
-
16
-
-
0033974913
-
Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms
-
Rahman S, Lake BD, Taanman JW, Hanna MG, Cooper JM, Schapira AH, Leonard JV. Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms. Brain 2000; 123: 591-600.
-
(2000)
Brain
, vol.123
, pp. 591-600
-
-
Rahman, S.1
Lake, B.D.2
Taanman, J.W.3
Hanna, M.G.4
Cooper, J.M.5
Schapira, A.H.6
Leonard, J.V.7
-
17
-
-
61449091466
-
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects
-
De Paepe B, Smet J, Lammens M, Seneca S, Martin JJ, De Bleecker J, De Meirleir L, Lissens W, Van Coster R. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects. J Clin Pathol 2009; 62: 172-6.
-
(2009)
J Clin Pathol
, vol.62
, pp. 172-176
-
-
De Paepe, B.1
Smet, J.2
Lammens, M.3
Seneca, S.4
Martin, J.J.5
De Bleecker, J.6
De Meirleir, L.7
Lissens, W.8
Van Coster, R.9
-
18
-
-
0027388963
-
Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications
-
Johnson MA, Bindoff LA, Turnbull DM. Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications. Ann Neurol 1993; 33: 28-35.
-
(1993)
Ann Neurol
, vol.33
, pp. 28-35
-
-
Johnson, M.A.1
Bindoff, L.A.2
Turnbull, D.M.3
-
19
-
-
77955863883
-
Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles
-
Yu-Wai-Man P, Lai-Cheong J, Borthwick GM, He L, Taylor GA, Greaves LC, Taylor RW, Griffiths PG, Turnbull DM. Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles. Invest Ophthalmol Vis Sci 2010; 51: 3347-53.
-
(2010)
Invest Ophthalmol Vis Sci
, vol.51
, pp. 3347-3353
-
-
Yu-Wai-Man, P.1
Lai-Cheong, J.2
Borthwick, G.M.3
He, L.4
Taylor, G.A.5
Greaves, L.C.6
Taylor, R.W.7
Griffiths, P.G.8
Turnbull, D.M.9
-
20
-
-
79953291261
-
Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis
-
Campbell GR, Ziabreva I, Reeve AK, Krishnan KJ, Reynolds R, Howell O, Lassmann H, Turnbull DM, Mahad DJ. Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis. Ann Neurol 2011; 69: 481-92.
-
(2011)
Ann Neurol
, vol.69
, pp. 481-492
-
-
Campbell, G.R.1
Ziabreva, I.2
Reeve, A.K.3
Krishnan, K.J.4
Reynolds, R.5
Howell, O.6
Lassmann, H.7
Turnbull, D.M.8
Mahad, D.J.9
-
21
-
-
17044456392
-
Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR
-
He L, Chinnery PF, Durham SE, Blakely EL, Wardell TM, Borthwick GM, Taylor RW, Turnbull DM. Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR. Nucleic Acids Res 2002; 30: e68.
-
(2002)
Nucleic Acids Res
, vol.30
-
-
He, L.1
Chinnery, P.F.2
Durham, S.E.3
Blakely, E.L.4
Wardell, T.M.5
Borthwick, G.M.6
Taylor, R.W.7
Turnbull, D.M.8
-
22
-
-
34548656405
-
A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells
-
Krishnan KJ, Bender A, Taylor RW, Turnbull DM. A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells. Anal Biochem 2007; 370: 127-9.
-
(2007)
Anal Biochem
, vol.370
, pp. 127-129
-
-
Krishnan, K.J.1
Bender, A.2
Taylor, R.W.3
Turnbull, D.M.4
-
23
-
-
57649210205
-
Mitochondrial DNA mutations in disease, aging, and neurodegeneration
-
Reeve AK, Krishnan KJ, Turnbull D. Mitochondrial DNA mutations in disease, aging, and neurodegeneration. Ann N Y Acad Sci 2008; 1147: 21-9.
-
(2008)
Ann N Y Acad Sci
, vol.1147
, pp. 21-29
-
-
Reeve, A.K.1
Krishnan, K.J.2
Turnbull, D.3
-
25
-
-
0026601317
-
Two myogenic lineages within the developing somite
-
Ordahl CP, Le Douarin NM. Two myogenic lineages within the developing somite. Development 1992; 114: 339-53.
-
(1992)
Development
, vol.114
, pp. 339-353
-
-
Ordahl, C.P.1
Le Douarin, N.M.2
-
26
-
-
0023762877
-
Mechanisms of vertebrate segmentation
-
Keynes RJ, Stern CD. Mechanisms of vertebrate segmentation. Development 1988; 103: 413-29.
-
(1988)
Development
, vol.103
, pp. 413-429
-
-
Keynes, R.J.1
Stern, C.D.2
-
27
-
-
77953136932
-
Regional myosin heavy chain distribution in selected paraspinal muscles
-
Regev GJ, Kim CW, Thacker BE, Tomiya A, Garfin SR, Ward SR, Lieber RL. Regional myosin heavy chain distribution in selected paraspinal muscles. Spine (Phila Pa 1976) 2010; 35: 1265-70.
-
(2010)
Spine (Phila Pa 1976)
, vol.35
, pp. 1265-1270
-
-
Regev, G.J.1
Kim, C.W.2
Thacker, B.E.3
Tomiya, A.4
Garfin, S.R.5
Ward, S.R.6
Lieber, R.L.7
-
28
-
-
39749124232
-
What causes mitochondrial DNA deletions in human cells?
-
Krishnan KJ, Reeve AK, Samuels DC, Chinnery PF, Blackwood JK, Taylor RW, Wanrooij S, Spelbrink JN, Lightowlers RN, Turnbull DM. What causes mitochondrial DNA deletions in human cells? Nat Genet 2008; 40: 275-9.
-
(2008)
Nat Genet
, vol.40
, pp. 275-279
-
-
Krishnan, K.J.1
Reeve, A.K.2
Samuels, D.C.3
Chinnery, P.F.4
Blackwood, J.K.5
Taylor, R.W.6
Wanrooij, S.7
Spelbrink, J.N.8
Lightowlers, R.N.9
Turnbull, D.M.10
-
29
-
-
0035097502
-
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age
-
Elson JL, Samuels DC, Turnbull DM, Chinnery PF. Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age. Am J Hum Genet 2001; 68: 802-6.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 802-806
-
-
Elson, J.L.1
Samuels, D.C.2
Turnbull, D.M.3
Chinnery, P.F.4
-
30
-
-
67649756839
-
On the timing and the extent of clonal expansion of mtDNA deletions: evidence from single-molecule PCR
-
Nicholas A, Kraytsberg Y, Guo X, Khrapko K. On the timing and the extent of clonal expansion of mtDNA deletions: evidence from single-molecule PCR. Exp Neurol 2009; 218: 316-19.
-
(2009)
Exp Neurol
, vol.218
, pp. 316-319
-
-
Nicholas, A.1
Kraytsberg, Y.2
Guo, X.3
Khrapko, K.4
-
31
-
-
36248937816
-
Transcriptional pathways associated with skeletal muscle disuse atrophy in humans
-
Chen YW, Gregory CM, Scarborough MT, Shi R, Walter GA, Vandenborne K. Transcriptional pathways associated with skeletal muscle disuse atrophy in humans. Physiol Genomics 2007; 31: 510-20.
-
(2007)
Physiol Genomics
, vol.31
, pp. 510-520
-
-
Chen, Y.W.1
Gregory, C.M.2
Scarborough, M.T.3
Shi, R.4
Walter, G.A.5
Vandenborne, K.6
-
32
-
-
0033917463
-
Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis
-
Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, Heinze HJ, Elger CE, Schubert W, Kunz WS. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain 2000; 123: 1339-48.
-
(2000)
Brain
, vol.123
, pp. 1339-1348
-
-
Vielhaber, S.1
Kunz, D.2
Winkler, K.3
Wiedemann, F.R.4
Kirches, E.5
Feistner, H.6
Heinze, H.J.7
Elger, C.E.8
Schubert, W.9
Kunz, W.S.10
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