-
1
-
-
0029374372
-
Profiles of neuromuscular diseases. Duchenne muscular dystrophy
-
McDonald C.M., Abresch R.T., Carter G.T., et al. Profiles of neuromuscular diseases. Duchenne muscular dystrophy. Am J Phys Med Rehabil 1995, 74:S70-92.
-
(1995)
Am J Phys Med Rehabil
, vol.74
, pp. S70-92
-
-
McDonald, C.M.1
Abresch, R.T.2
Carter, G.T.3
-
2
-
-
0024600393
-
Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy
-
Brooke M.H., Fenichel G.M., Griggs R.C., et al. Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy. Neurology 1989, 39:475-481.
-
(1989)
Neurology
, vol.39
, pp. 475-481
-
-
Brooke, M.H.1
Fenichel, G.M.2
Griggs, R.C.3
-
3
-
-
28544447912
-
The muscular dystrophies: from genes to therapies
-
Lovering R.M., Porter N.C., Bloch R.J. The muscular dystrophies: from genes to therapies. Phys Ther 2005, 85:1372-1388.
-
(2005)
Phys Ther
, vol.85
, pp. 1372-1388
-
-
Lovering, R.M.1
Porter, N.C.2
Bloch, R.J.3
-
4
-
-
0027980295
-
Increasing complexity of the dystrophin-associated protein complex
-
Tinsley J.M., Blake D.J., Zuellig R.A., Davies K.E. Increasing complexity of the dystrophin-associated protein complex. Proc Natl Acad Sci U S A 1994, 91:8307-8313.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 8307-8313
-
-
Tinsley, J.M.1
Blake, D.J.2
Zuellig, R.A.3
Davies, K.E.4
-
5
-
-
0029921129
-
Utrophin: a structural and functional comparison to dystrophin
-
Blake D.J., Tinsley J.M., Davies K.E. Utrophin: a structural and functional comparison to dystrophin. Brain Pathol 1996, 6:37-47.
-
(1996)
Brain Pathol
, vol.6
, pp. 37-47
-
-
Blake, D.J.1
Tinsley, J.M.2
Davies, K.E.3
-
7
-
-
0036156243
-
Brain function in Duchenne muscular dystrophy
-
Anderson J.L., Head S.I., Rae C., Morley J.W. Brain function in Duchenne muscular dystrophy. Brain 2002, 125:4-13.
-
(2002)
Brain
, vol.125
, pp. 4-13
-
-
Anderson, J.L.1
Head, S.I.2
Rae, C.3
Morley, J.W.4
-
9
-
-
16844369869
-
Association between intellectual functioning and age in children and young adults with Duchenne muscular dystrophy: further results from a meta-analysis
-
Cotton S.M., Voudouris N.J., Greenwood K.M. Association between intellectual functioning and age in children and young adults with Duchenne muscular dystrophy: further results from a meta-analysis. Dev Med Child Neurol 2005, 47:257-265.
-
(2005)
Dev Med Child Neurol
, vol.47
, pp. 257-265
-
-
Cotton, S.M.1
Voudouris, N.J.2
Greenwood, K.M.3
-
10
-
-
33847391558
-
Verbal and memory skills in males with Duchenne muscular dystrophy
-
Hinton V.J., Fee R.J., Goldstein E.M., De Vivo D.C. Verbal and memory skills in males with Duchenne muscular dystrophy. Dev Med Child Neurol 2007, 49:123-128.
-
(2007)
Dev Med Child Neurol
, vol.49
, pp. 123-128
-
-
Hinton, V.J.1
Fee, R.J.2
Goldstein, E.M.3
De Vivo, D.C.4
-
11
-
-
78650171188
-
Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne muscular dystrophy
-
Wingeier K., Giger E., Strozzi S., et al. Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne muscular dystrophy. J Clin Neurosci 2011, 18:90-95.
-
(2011)
J Clin Neurosci
, vol.18
, pp. 90-95
-
-
Wingeier, K.1
Giger, E.2
Strozzi, S.3
-
12
-
-
0034933730
-
Intelligence and Duchenne muscular dystrophy: full-scale, verbal, and performance intelligence quotients
-
Cotton S., Voudouris N.J., Greenwood K.M. Intelligence and Duchenne muscular dystrophy: full-scale, verbal, and performance intelligence quotients. Dev Med Child Neurol 2001, 43:497-501.
-
(2001)
Dev Med Child Neurol
, vol.43
, pp. 497-501
-
-
Cotton, S.1
Voudouris, N.J.2
Greenwood, K.M.3
-
13
-
-
1342282774
-
Specific cognitive deficits are common in children with Duchenne muscular dystrophy
-
Wicksell R.K., Kihlgren M., Melin L., Eeg-Olofsson O. Specific cognitive deficits are common in children with Duchenne muscular dystrophy. Dev Med Child Neurol 2004, 46:154-159.
-
(2004)
Dev Med Child Neurol
, vol.46
, pp. 154-159
-
-
Wicksell, R.K.1
Kihlgren, M.2
Melin, L.3
Eeg-Olofsson, O.4
-
14
-
-
34249701745
-
Evaluation of narrative abilities in patients suffering from duchenne muscular dystrophy
-
Marini A., Lorusso M.L., D'Angelo M.G., et al. Evaluation of narrative abilities in patients suffering from duchenne muscular dystrophy. Brain Lang 2007, 102:1-12.
-
(2007)
Brain Lang
, vol.102
, pp. 1-12
-
-
Marini, A.1
Lorusso, M.L.2
D'Angelo, M.G.3
-
15
-
-
0026039523
-
Passive avoidance behaviour deficit in the mdx mouse
-
Muntoni F., Mateddu A., Serra G. Passive avoidance behaviour deficit in the mdx mouse. Neuromuscul Disord 1991, 1:121-123.
-
(1991)
Neuromuscul Disord
, vol.1
, pp. 121-123
-
-
Muntoni, F.1
Mateddu, A.2
Serra, G.3
-
16
-
-
84860492770
-
Upregulation of brain utrophin does not rescue behavioral alterations in dystrophin-deficient mice
-
Perronnet C., Chagneau C., Le B.P., et al. Upregulation of brain utrophin does not rescue behavioral alterations in dystrophin-deficient mice. Hum Mol Genet 2012, 21:2263-2276.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 2263-2276
-
-
Perronnet, C.1
Chagneau, C.2
Le, B.P.3
-
17
-
-
0028834843
-
Influence of dystrophin-gene mutation on mdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks
-
Vaillend C., Rendon A., Misslin R., Ungerer A. Influence of dystrophin-gene mutation on mdx mouse behavior. I. Retention deficits at long delays in spontaneous alternation and bar-pressing tasks. Behav Genet 1995, 25:569-579.
-
(1995)
Behav Genet
, vol.25
, pp. 569-579
-
-
Vaillend, C.1
Rendon, A.2
Misslin, R.3
Ungerer, A.4
-
18
-
-
0018849476
-
Central nervous system involvement in progressive muscular dystrophy
-
Yoshioka M., Okuno T., Honda Y., Nakano Y. Central nervous system involvement in progressive muscular dystrophy. Arch Dis Child 1980, 55:589-594.
-
(1980)
Arch Dis Child
, vol.55
, pp. 589-594
-
-
Yoshioka, M.1
Okuno, T.2
Honda, Y.3
Nakano, Y.4
-
19
-
-
0032977092
-
A novel deletion of the dystrophin S-promoter region cosegregating with mental retardation
-
Chen D.H., Takeshima Y., Ishikawa Y., Ishikawa Y., Minami R., Matsuo M. A novel deletion of the dystrophin S-promoter region cosegregating with mental retardation. Neurology 1999, 52:638-640.
-
(1999)
Neurology
, vol.52
, pp. 638-640
-
-
Chen, D.H.1
Takeshima, Y.2
Ishikawa, Y.3
Ishikawa, Y.4
Minami, R.5
Matsuo, M.6
-
20
-
-
0032497562
-
Brain biochemistry in Duchenne muscular dystrophy: a 1H magnetic resonance and neuropsychological study
-
Rae C., Scott R.B., Thompson C.H., et al. Brain biochemistry in Duchenne muscular dystrophy: a 1H magnetic resonance and neuropsychological study. J Neurol Sci 1998, 160:148-157.
-
(1998)
J Neurol Sci
, vol.160
, pp. 148-157
-
-
Rae, C.1
Scott, R.B.2
Thompson, C.H.3
-
21
-
-
79952635520
-
Brain metabolite composition in relation to cognitive function and dystrophin mutations in boys with Duchenne muscular dystrophy
-
Kreis R., Wingeier K., Vermathen P., et al. Brain metabolite composition in relation to cognitive function and dystrophin mutations in boys with Duchenne muscular dystrophy. NMR Biomed 2011, 24:253-262.
-
(2011)
NMR Biomed
, vol.24
, pp. 253-262
-
-
Kreis, R.1
Wingeier, K.2
Vermathen, P.3
-
22
-
-
0030586992
-
An in vivo and in vitro H-magnetic resonance spectroscopy study of mdx mouse brain: abnormal development or neural necrosis?
-
Tracey I., Dunn J.F., Parkes H.G., Radda G.K. An in vivo and in vitro H-magnetic resonance spectroscopy study of mdx mouse brain: abnormal development or neural necrosis?. J Neurol Sci 1996, 141:13-18.
-
(1996)
J Neurol Sci
, vol.141
, pp. 13-18
-
-
Tracey, I.1
Dunn, J.F.2
Parkes, H.G.3
Radda, G.K.4
-
23
-
-
38649105136
-
Duchenne muscular dystrophy: a cerebellar disorder?
-
Cyrulnik S.E., Hinton V.J. Duchenne muscular dystrophy: a cerebellar disorder?. Neurosci Biobehav Rev 2008, 32:486-496.
-
(2008)
Neurosci Biobehav Rev
, vol.32
, pp. 486-496
-
-
Cyrulnik, S.E.1
Hinton, V.J.2
-
24
-
-
0029975308
-
Brain metabolism is abnormal in the mdx model of Duchenne muscular dystrophy
-
Tracey I., Dunn J.F., Radda G.K. Brain metabolism is abnormal in the mdx model of Duchenne muscular dystrophy. Brain 1996, 119(Pt 3):1039-1044.
-
(1996)
Brain
, vol.119
, pp. 1039-1044
-
-
Tracey, I.1
Dunn, J.F.2
Radda, G.K.3
-
25
-
-
0028211227
-
Dystrophin and dystrophin-related protein in the brains of normal and mdx mice
-
Uchino M., Yoshioka K., Miike T., et al. Dystrophin and dystrophin-related protein in the brains of normal and mdx mice. Muscle Nerve 1994, 17:533-538.
-
(1994)
Muscle Nerve
, vol.17
, pp. 533-538
-
-
Uchino, M.1
Yoshioka, K.2
Miike, T.3
-
26
-
-
0023904860
-
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
-
Koenig M., Monaco A.P., Kunkel L.M. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell 1988, 53:219-228.
-
(1988)
Cell
, vol.53
, pp. 219-228
-
-
Koenig, M.1
Monaco, A.P.2
Kunkel, L.M.3
-
27
-
-
0025880635
-
What does dystrophin do in normal muscle?
-
Lansman J.B., Franco A. What does dystrophin do in normal muscle?. J Muscle Res Cell Motil 1991, 12:409-411.
-
(1991)
J Muscle Res Cell Motil
, vol.12
, pp. 409-411
-
-
Lansman, J.B.1
Franco, A.2
-
29
-
-
0031974345
-
Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
-
Gee S.H., Madhavan R., Levinson S.R., Caldwell J.H., Sealock R., Froehner S.C. Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins. J Neurosci 1998, 18:128-137.
-
(1998)
J Neurosci
, vol.18
, pp. 128-137
-
-
Gee, S.H.1
Madhavan, R.2
Levinson, S.R.3
Caldwell, J.H.4
Sealock, R.5
Froehner, S.C.6
-
30
-
-
0033612935
-
Dystrophin is required for organizing large acetylcholine receptor aggregates
-
Kong J., Anderson J.E. Dystrophin is required for organizing large acetylcholine receptor aggregates. Brain Res 1999, 839:298-304.
-
(1999)
Brain Res
, vol.839
, pp. 298-304
-
-
Kong, J.1
Anderson, J.E.2
-
31
-
-
84872417904
-
Effects of in vivo injury on the neuromuscular junction in healthy and dystrophic muscles
-
Pratt S.J., Shah S.B., Ward C.W., Inacio M.P., Stains J.P., Lovering R.M. Effects of in vivo injury on the neuromuscular junction in healthy and dystrophic muscles. J Physiol 2013, 591:559-570.
-
(2013)
J Physiol
, vol.591
, pp. 559-570
-
-
Pratt, S.J.1
Shah, S.B.2
Ward, C.W.3
Inacio, M.P.4
Stains, J.P.5
Lovering, R.M.6
-
32
-
-
84864876833
-
Microtubules underlie dysfunction in duchenne muscular dystrophy
-
Khairallah R.J., Shi G., Sbrana F., et al. Microtubules underlie dysfunction in duchenne muscular dystrophy. Sci Signal 2012, 5:ra56.
-
(2012)
Sci Signal
, vol.5
, pp. ra56
-
-
Khairallah, R.J.1
Shi, G.2
Sbrana, F.3
-
33
-
-
33745168598
-
Muscle damage in mdx (dystrophic) mice: role of calcium and reactive oxygen species
-
Whitehead N.P., Yeung E.W., Allen D.G. Muscle damage in mdx (dystrophic) mice: role of calcium and reactive oxygen species. Clin Exp Pharmacol Physiol 2006, 33:657-662.
-
(2006)
Clin Exp Pharmacol Physiol
, vol.33
, pp. 657-662
-
-
Whitehead, N.P.1
Yeung, E.W.2
Allen, D.G.3
-
35
-
-
84875370616
-
In vivo high-resolution localized (1) H MR spectroscopy in the awake rat brain at 7 T
-
Xu S., Ji Y., Chen X., Yang Y., Gullapalli R.P., Masri R. In vivo high-resolution localized (1) H MR spectroscopy in the awake rat brain at 7 T. Magn Reson Med 2013, 69:937-943.
-
(2013)
Magn Reson Med
, vol.69
, pp. 937-943
-
-
Xu, S.1
Ji, Y.2
Chen, X.3
Yang, Y.4
Gullapalli, R.P.5
Masri, R.6
-
36
-
-
0034959727
-
Automatic quantitation of localized in vivo 1H spectra with LCModel
-
Provencher S.W. Automatic quantitation of localized in vivo 1H spectra with LCModel. NMR Biomed 2001, 14:260-264.
-
(2001)
NMR Biomed
, vol.14
, pp. 260-264
-
-
Provencher, S.W.1
-
37
-
-
80054110405
-
Diffusion kurtosis as an in vivo imaging marker for reactive astrogliosis in traumatic brain injury
-
Zhuo J., Xu S., Proctor J.L., et al. Diffusion kurtosis as an in vivo imaging marker for reactive astrogliosis in traumatic brain injury. Neuroimage 2012, 59:467-477.
-
(2012)
Neuroimage
, vol.59
, pp. 467-477
-
-
Zhuo, J.1
Xu, S.2
Proctor, J.L.3
-
38
-
-
49249138157
-
Comparative analysis of the frequency and distribution of stem and progenitor cells in the adult mouse brain
-
Golmohammadi M.G., Blackmore D.G., Large B., et al. Comparative analysis of the frequency and distribution of stem and progenitor cells in the adult mouse brain. Stem Cells 2008, 26:979-987.
-
(2008)
Stem Cells
, vol.26
, pp. 979-987
-
-
Golmohammadi, M.G.1
Blackmore, D.G.2
Large, B.3
-
39
-
-
0036839039
-
Molecular pathophysiology of myofiber injury in deficiencies of the dystrophin-glycoprotein complex
-
Petrof B.J. Molecular pathophysiology of myofiber injury in deficiencies of the dystrophin-glycoprotein complex. Am J Phys Med Rehabil 2002, 81:S162-74.
-
(2002)
Am J Phys Med Rehabil
, vol.81
, pp. S162-S174
-
-
Petrof, B.J.1
-
40
-
-
0035190381
-
The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies
-
Rando T.A. The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies. Muscle Nerve 2001, 24:1575-1594.
-
(2001)
Muscle Nerve
, vol.24
, pp. 1575-1594
-
-
Rando, T.A.1
-
41
-
-
0344420060
-
Dystrophin and mutations: one gene, several proteins, multiple phenotypes
-
Muntoni F., Torelli S., Ferlini A. Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet Neurol 2003, 2:731-740.
-
(2003)
Lancet Neurol
, vol.2
, pp. 731-740
-
-
Muntoni, F.1
Torelli, S.2
Ferlini, A.3
-
42
-
-
0035032229
-
Biochemical and histochemical analysis of 71 kDa dystrophin isoform (Dp71f) in rat brain
-
Garcia-Tovar C.G., Perez A., Luna J., et al. Biochemical and histochemical analysis of 71 kDa dystrophin isoform (Dp71f) in rat brain. Acta Histochem 2001, 103:209-224.
-
(2001)
Acta Histochem
, vol.103
, pp. 209-224
-
-
Garcia-Tovar, C.G.1
Perez, A.2
Luna, J.3
-
43
-
-
70349573300
-
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression
-
Daoud F., Angeard N., Demerre B., et al. Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression. Hum Mol Genet 2009, 18:3779-3794.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3779-3794
-
-
Daoud, F.1
Angeard, N.2
Demerre, B.3
-
44
-
-
0033920086
-
Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening
-
Moizard M.P., Toutain A., Fournier D., et al. Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening. Eur J Hum Genet 2000, 8:552-556.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 552-556
-
-
Moizard, M.P.1
Toutain, A.2
Fournier, D.3
-
45
-
-
77649282617
-
Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophy
-
Taylor P.J., Betts G.A., Maroulis S., et al. Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophy. PLoS ONE 2010, 5:e8803.
-
(2010)
PLoS ONE
, vol.5
, pp. e8803
-
-
Taylor, P.J.1
Betts, G.A.2
Maroulis, S.3
-
46
-
-
0027484533
-
Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients
-
Lenk U., Hanke R., Thiele H., Speer A. Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients. Hum Mol Genet 1993, 2:1877-1881.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1877-1881
-
-
Lenk, U.1
Hanke, R.2
Thiele, H.3
Speer, A.4
-
47
-
-
1542381809
-
Diversity of the brain dystrophin-glycoprotein complex
-
Culligan K., Ohlendieck K. Diversity of the brain dystrophin-glycoprotein complex. J Biomed Biotechnol 2002, 2:31-36.
-
(2002)
J Biomed Biotechnol
, vol.2
, pp. 31-36
-
-
Culligan, K.1
Ohlendieck, K.2
-
48
-
-
0025648083
-
Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons
-
Lidov H.G., Byers T.J., Watkins S.C., Kunkel L.M. Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons. Nature 1990, 348:725-728.
-
(1990)
Nature
, vol.348
, pp. 725-728
-
-
Lidov, H.G.1
Byers, T.J.2
Watkins, S.C.3
Kunkel, L.M.4
-
49
-
-
0026474587
-
Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy
-
Kim T.W., Wu K., Xu J.L., Black I.B. Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy. Proc Natl Acad Sci U S A 1992, 89:11642-11644.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 11642-11644
-
-
Kim, T.W.1
Wu, K.2
Xu, J.L.3
Black, I.B.4
-
50
-
-
0038407772
-
Severe alterations of endothelial and glial cells in the blood-brain barrier of dystrophic mdx mice
-
Nico B., Frigeri A., Nicchia G.P., et al. Severe alterations of endothelial and glial cells in the blood-brain barrier of dystrophic mdx mice. Glia 2003, 42:235-251.
-
(2003)
Glia
, vol.42
, pp. 235-251
-
-
Nico, B.1
Frigeri, A.2
Nicchia, G.P.3
-
51
-
-
84907169008
-
Lack of dystrophin results in abnormal cerebral diffusion and perfusion in vivo
-
Goodnough C.L., Gao Y., Li X., et al. Lack of dystrophin results in abnormal cerebral diffusion and perfusion in vivo. Neuroimage 2014, 102(Pt 2):809-816.
-
(2014)
Neuroimage
, vol.102
, pp. 809-816
-
-
Goodnough, C.L.1
Gao, Y.2
Li, X.3
-
52
-
-
2442715460
-
Taurine transporter knockout depletes muscle taurine levels and results in severe skeletal muscle impairment but leaves cardiac function uncompromised
-
Warskulat U., Flogel U., Jacoby C., et al. Taurine transporter knockout depletes muscle taurine levels and results in severe skeletal muscle impairment but leaves cardiac function uncompromised. FASEB J 2004, 18:577-579.
-
(2004)
FASEB J
, vol.18
, pp. 577-579
-
-
Warskulat, U.1
Flogel, U.2
Jacoby, C.3
-
53
-
-
0026595620
-
Physiological actions of taurine
-
Huxtable R.J. Physiological actions of taurine. Physiol Rev 1992, 72:101-163.
-
(1992)
Physiol Rev
, vol.72
, pp. 101-163
-
-
Huxtable, R.J.1
-
55
-
-
55349131743
-
Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice
-
Hollingworth S., Zeiger U., Baylor S.M. Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice. J Physiol 2008, 586:5063-5075.
-
(2008)
J Physiol
, vol.586
, pp. 5063-5075
-
-
Hollingworth, S.1
Zeiger, U.2
Baylor, S.M.3
-
56
-
-
2942696374
-
The action potential-evoked sarcoplasmic reticulum calcium release is impaired in mdx mouse muscle fibres
-
Woods C.E., Novo D., DiFranco M., Vergara J.L. The action potential-evoked sarcoplasmic reticulum calcium release is impaired in mdx mouse muscle fibres. J Physiol 2004, 557:59-75.
-
(2004)
J Physiol
, vol.557
, pp. 59-75
-
-
Woods, C.E.1
Novo, D.2
DiFranco, M.3
Vergara, J.L.4
-
58
-
-
85003758675
-
Disruption of action potential and calcium signaling properties in malformed myofibers from dystrophin-deficient mice
-
Hernandez-Ochoa E.O., Pratt S.J., Garcia-Pelagio K.P., Schneider M.F., Lovering R.M. Disruption of action potential and calcium signaling properties in malformed myofibers from dystrophin-deficient mice. Physiol Rep 2015, 3(4):e12366. pii. 10.14814/phy2.12366.
-
(2015)
Physiol Rep
, vol.3
, Issue.4
, pp. e12366
-
-
Hernandez-Ochoa, E.O.1
Pratt, S.J.2
Garcia-Pelagio, K.P.3
Schneider, M.F.4
Lovering, R.M.5
-
59
-
-
27844464496
-
Propagation in the transverse tubular system and voltage dependence of calcium release in normal and mdx muscle fibres
-
Woods C.E., Novo D., DiFranco M., Capote J., Vergara J.L. Propagation in the transverse tubular system and voltage dependence of calcium release in normal and mdx muscle fibres. J Physiol 2005, 568:867-880.
-
(2005)
J Physiol
, vol.568
, pp. 867-880
-
-
Woods, C.E.1
Novo, D.2
DiFranco, M.3
Capote, J.4
Vergara, J.L.5
-
62
-
-
0018758714
-
Catalase, superoxide dismutase, glutathione reductase and thiobarbituric acid-reactive products in normal and dystrophic human muscle
-
Kar N.C., Pearson C.M. Catalase, superoxide dismutase, glutathione reductase and thiobarbituric acid-reactive products in normal and dystrophic human muscle. Clin Chim Acta 1979, 94:277-280.
-
(1979)
Clin Chim Acta
, vol.94
, pp. 277-280
-
-
Kar, N.C.1
Pearson, C.M.2
-
63
-
-
0021236449
-
Changes in superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase activities and thiobarbituric acid-reactive products levels in early stages of development in dystrophic chickens
-
Mizuno Y. Changes in superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase activities and thiobarbituric acid-reactive products levels in early stages of development in dystrophic chickens. Exp Neurol 1984, 84:58-73.
-
(1984)
Exp Neurol
, vol.84
, pp. 58-73
-
-
Mizuno, Y.1
-
64
-
-
0022480606
-
Activities of antioxidant enzymes in muscle, liver and lung of chickens with inherited muscular dystrophy
-
Murphy M.E., Kehrer J.P. Activities of antioxidant enzymes in muscle, liver and lung of chickens with inherited muscular dystrophy. Biochem Biophys Res Commun 1986, 134:550-556.
-
(1986)
Biochem Biophys Res Commun
, vol.134
, pp. 550-556
-
-
Murphy, M.E.1
Kehrer, J.P.2
-
65
-
-
0036133505
-
Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse
-
Rae C., Griffin J.L., Blair D.H., et al. Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse. Neuromuscul Disord 2002, 12:121-129.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 121-129
-
-
Rae, C.1
Griffin, J.L.2
Blair, D.H.3
-
66
-
-
0022471783
-
Reduced phosphorylcholine hydrolysis by homogenates of temporal regions of Alzheimer's brain
-
Kanfer J.N., McCartney D.G. Reduced phosphorylcholine hydrolysis by homogenates of temporal regions of Alzheimer's brain. Biochem Biophys Res Commun 1986, 139:315-319.
-
(1986)
Biochem Biophys Res Commun
, vol.139
, pp. 315-319
-
-
Kanfer, J.N.1
McCartney, D.G.2
-
67
-
-
0023818756
-
31P nuclear magnetic resonance study of the brain in Alzheimer's disease
-
Pettegrew J.W., Moossy J., Withers G., McKeag D., Panchalingam K. 31P nuclear magnetic resonance study of the brain in Alzheimer's disease. J Neuropathol Exp Neurol 1988, 47:235-248.
-
(1988)
J Neuropathol Exp Neurol
, vol.47
, pp. 235-248
-
-
Pettegrew, J.W.1
Moossy, J.2
Withers, G.3
McKeag, D.4
Panchalingam, K.5
-
68
-
-
0032924418
-
Oxidative inactivation of brain alkaline phosphatase responsible for hydrolysis of phosphocholine
-
Sok D.E. Oxidative inactivation of brain alkaline phosphatase responsible for hydrolysis of phosphocholine. J Neurochem 1999, 72:355-362.
-
(1999)
J Neurochem
, vol.72
, pp. 355-362
-
-
Sok, D.E.1
-
69
-
-
45549091580
-
Between channels and tears: aim at ROS to save the membrane of dystrophic fibres
-
Reggiani C. Between channels and tears: aim at ROS to save the membrane of dystrophic fibres. J Physiol 2008, 586:1779.
-
(2008)
J Physiol
, vol.586
, pp. 1779
-
-
Reggiani, C.1
-
70
-
-
0033258164
-
Short communication: altered synaptic clustering of GABAA receptors in mice lacking dystrophin (mdx mice)
-
Knuesel I., Mastrocola M., Zuellig R.A., Bornhauser B., Schaub M.C., Fritschy J.M. Short communication: altered synaptic clustering of GABAA receptors in mice lacking dystrophin (mdx mice). Eur J Neurosci 1999, 11:4457-4462.
-
(1999)
Eur J Neurosci
, vol.11
, pp. 4457-4462
-
-
Knuesel, I.1
Mastrocola, M.2
Zuellig, R.A.3
Bornhauser, B.4
Schaub, M.C.5
Fritschy, J.M.6
-
71
-
-
84925507915
-
Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers
-
Goyenvalle A., Griffith G., Babbs A., et al. Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers. Nat Med 2015, 21:270-275.
-
(2015)
Nat Med
, vol.21
, pp. 270-275
-
-
Goyenvalle, A.1
Griffith, G.2
Babbs, A.3
-
72
-
-
34347374860
-
Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma
-
Chamberlain J.S., Metzger J., Reyes M., Townsend D., Faulkner J.A. Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma. FASEB J 2007, 21:2195-2204.
-
(2007)
FASEB J
, vol.21
, pp. 2195-2204
-
-
Chamberlain, J.S.1
Metzger, J.2
Reyes, M.3
Townsend, D.4
Faulkner, J.A.5
-
73
-
-
0023780812
-
Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy
-
Glesby M.J., Rosenmann E., Nylen E.G., Wrogemann K. Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy. Muscle Nerve 1988, 11:852-856.
-
(1988)
Muscle Nerve
, vol.11
, pp. 852-856
-
-
Glesby, M.J.1
Rosenmann, E.2
Nylen, E.G.3
Wrogemann, K.4
-
74
-
-
0027751262
-
Muscular weakness in the mdx mouse
-
Muntoni F., Mateddu A., Marchei F., Clerk A., Serra G. Muscular weakness in the mdx mouse. J Neurol Sci 1993, 120:71-77.
-
(1993)
J Neurol Sci
, vol.120
, pp. 71-77
-
-
Muntoni, F.1
Mateddu, A.2
Marchei, F.3
Clerk, A.4
Serra, G.5
-
75
-
-
0033007573
-
Characteristics of skeletal muscle in mdx mutant mice
-
De la P.S., Morin S., Koenig J. Characteristics of skeletal muscle in mdx mutant mice. Int Rev Cytol 1999, 191:99-148.
-
(1999)
Int Rev Cytol
, vol.191
, pp. 99-148
-
-
De la, P.S.1
Morin, S.2
Koenig, J.3
-
76
-
-
0021713536
-
Muscle development in mdx mutant mice
-
Dangain J., Vrbova G. Muscle development in mdx mutant mice. Muscle Nerve 1984, 7:700-704.
-
(1984)
Muscle Nerve
, vol.7
, pp. 700-704
-
-
Dangain, J.1
Vrbova, G.2
-
77
-
-
0014630886
-
The central nervous system in Duchenne muscular dystrophy
-
Dubowitz V., Crome L. The central nervous system in Duchenne muscular dystrophy. Brain 1969, 92:805-808.
-
(1969)
Brain
, vol.92
, pp. 805-808
-
-
Dubowitz, V.1
Crome, L.2
-
78
-
-
0027929953
-
Cognitive impairment in Duchenne muscular dystrophy
-
Bresolin N., Castelli E., Comi G.P., et al. Cognitive impairment in Duchenne muscular dystrophy. Neuromuscul Disord 1994, 4:359-369.
-
(1994)
Neuromuscul Disord
, vol.4
, pp. 359-369
-
-
Bresolin, N.1
Castelli, E.2
Comi, G.P.3
-
79
-
-
0021801023
-
Increased head circumference in patients with Duchenne muscular dystrophy
-
Schmidt B., Watters G.V., Rosenblatt B., Silver K. Increased head circumference in patients with Duchenne muscular dystrophy. Ann Neurol 1985, 17:620-621.
-
(1985)
Ann Neurol
, vol.17
, pp. 620-621
-
-
Schmidt, B.1
Watters, G.V.2
Rosenblatt, B.3
Silver, K.4
-
80
-
-
0025799702
-
Head circumference and intellectual performance of patients with Duchenne muscular dystrophy
-
Appleton R.E., Bushby K., Gardner-Medwin D., Welch J., Kelly P.J. Head circumference and intellectual performance of patients with Duchenne muscular dystrophy. Dev Med Child Neurol 1991, 33:884-890.
-
(1991)
Dev Med Child Neurol
, vol.33
, pp. 884-890
-
-
Appleton, R.E.1
Bushby, K.2
Gardner-Medwin, D.3
Welch, J.4
Kelly, P.J.5
-
81
-
-
0013977481
-
Mental deficiency associated with muscular dystrophy. A neuropathological study
-
Rosman N.P., Kakulas B.A. Mental deficiency associated with muscular dystrophy. A neuropathological study. Brain 1966, 89:769-788.
-
(1966)
Brain
, vol.89
, pp. 769-788
-
-
Rosman, N.P.1
Kakulas, B.A.2
-
82
-
-
0014774537
-
The cerebral defect and myopathy in Duchenne muscular dystrophy. A comparative clinicopathological study
-
Rosman N.P. The cerebral defect and myopathy in Duchenne muscular dystrophy. A comparative clinicopathological study. Neurology 1970, 20:329-335.
-
(1970)
Neurology
, vol.20
, pp. 329-335
-
-
Rosman, N.P.1
-
83
-
-
0026274633
-
Mental development in Duchenne muscular dystrophy. Correlation of data of the brain scanner]
-
Septien L., Gras P., Borsotti J.P., Giroud M., Nivelon J.L., Dumas R. Mental development in Duchenne muscular dystrophy. Correlation of data of the brain scanner]. Pediatrie 1991, 46:817-819.
-
(1991)
Pediatrie
, vol.46
, pp. 817-819
-
-
Septien, L.1
Gras, P.2
Borsotti, J.P.3
Giroud, M.4
Nivelon, J.L.5
Dumas, R.6
-
84
-
-
0025357201
-
Etiology of intellectual impairment in Duchenne muscular dystrophy
-
al-Qudah A.A., Kobayashi J., Chuang S., Dennis M., Ray P. Etiology of intellectual impairment in Duchenne muscular dystrophy. Pediatr Neurol 1990, 6:57-59.
-
(1990)
Pediatr Neurol
, vol.6
, pp. 57-59
-
-
al-Qudah, A.A.1
Kobayashi, J.2
Chuang, S.3
Dennis, M.4
Ray, P.5
-
85
-
-
0025277792
-
The C57BL/10Bg sps/sps mouse: a mutant with absence-like seizures; neurochemical and behavioral correlates
-
Ortiz J.G., Negron A.E., Garcia M.T., Rosado J.E., Maldonaldo C.S. The C57BL/10Bg sps/sps mouse: a mutant with absence-like seizures; neurochemical and behavioral correlates. Neurosci Lett 1990, 114:231-236.
-
(1990)
Neurosci Lett
, vol.114
, pp. 231-236
-
-
Ortiz, J.G.1
Negron, A.E.2
Garcia, M.T.3
Rosado, J.E.4
Maldonaldo, C.S.5
-
86
-
-
79960242985
-
Reduced postsynaptic GABAA receptor number and enhanced gaboxadol induced change in holding currents in Purkinje cells of the dystrophin-deficient mdx mouse
-
Kueh S.L., Dempster J., Head S.I., Morley J.W. Reduced postsynaptic GABAA receptor number and enhanced gaboxadol induced change in holding currents in Purkinje cells of the dystrophin-deficient mdx mouse. Neurobiol Dis 2011, 43:558-564.
-
(2011)
Neurobiol Dis
, vol.43
, pp. 558-564
-
-
Kueh, S.L.1
Dempster, J.2
Head, S.I.3
Morley, J.W.4
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