-
1
-
-
0028905205
-
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
-
Richard, I., Broux, O., Allamand, V., Fougerousse, F., Chiannilkulchai, N., Bourg, N., Brenguier, L., Devaud, C., Pasturaud, P., Roudaut, C. et al. (1995) Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A. Cell, 81, 27-40.
-
(1995)
Cell
, vol.81
, pp. 27-40
-
-
Richard, I.1
Broux, O.2
Allamand, V.3
Fougerousse, F.4
Chiannilkulchai, N.5
Bourg, N.6
Brenguier, L.7
Devaud, C.8
Pasturaud, P.9
Roudaut, C.10
-
2
-
-
78149455943
-
Expanding members and roles of the calpain superfamily and their genetically modified animals
-
Sorimachi, H., Hata, S. and Ono, Y. (2010) Expanding members and roles of the calpain superfamily and their genetically modified animals. Exp. Anim., 59, 549-566.
-
(2010)
Exp. Anim.
, vol.59
, pp. 549-566
-
-
Sorimachi, H.1
Hata, S.2
Ono, Y.3
-
3
-
-
33846372980
-
Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)
-
Kramerova, I., Beckmann, J.S. and Spencer, M.J. (2007) Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A). Biochim. Biophys. Acta, 1772, 128-144.
-
(2007)
Biochim. Biophys. Acta
, vol.1772
, pp. 128-144
-
-
Kramerova, I.1
Beckmann, J.S.2
Spencer, M.J.3
-
4
-
-
33847232234
-
A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay
-
Milic, A., Daniele, N., Lochmuller, H., Mora, M., Comi, G.P., Moggio, M., Noulet, F., Walter, M.C., Morandi, L., Poupiot, J. et al. (2007) A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay. Neuromuscul. Disord., 17, 148-156.
-
(2007)
Neuromuscul. Disord.
, vol.17
, pp. 148-156
-
-
Milic, A.1
Daniele, N.2
Lochmuller, H.3
Mora, M.4
Comi, G.P.5
Moggio, M.6
Noulet, F.7
Walter, M.C.8
Morandi, L.9
Poupiot, J.10
-
5
-
-
0038337815
-
The calpain system
-
Goll, D.E., Thompson, V.F., Li, H., Wei, W. and Cong, J. (2003) The calpain system. Physiol. Rev., 83, 731-801.
-
(2003)
Physiol. Rev.
, vol.83
, pp. 731-801
-
-
Goll, D.E.1
Thompson, V.F.2
Li, H.3
Wei, W.4
Cong, J.5
-
6
-
-
3042597817
-
Insertion sequence 1 of muscle-specific calpain, p94, acts as an internal propeptide
-
Diaz, B.G., Moldoveanu, T., Kuiper, M.J., Campbell, R.L. and Davies, P.L. (2004) Insertion sequence 1 of muscle-specific calpain, p94, acts as an internal propeptide. J. Biol. Chem., 279, 27656-27666.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 27656-27666
-
-
Diaz, B.G.1
Moldoveanu, T.2
Kuiper, M.J.3
Campbell, R.L.4
Davies, P.L.5
-
7
-
-
0344629442
-
Calpain 3 is activated through autolysis within the active site and lyses sarcomeric and sarcolemmal components
-
Taveau, M., Bourg, N., Sillon, G., Roudaut, C., Bartoli, M. and Richard, I. (2003) Calpain 3 is activated through autolysis within the active site and lyses sarcomeric and sarcolemmal components. Mol. Cell Biol., 23, 9127-9135.
-
(2003)
Mol. Cell Biol.
, vol.23
, pp. 9127-9135
-
-
Taveau, M.1
Bourg, N.2
Sillon, G.3
Roudaut, C.4
Bartoli, M.5
Richard, I.6
-
8
-
-
54449100812
-
Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle
-
Kramerova, I., Kudryashova, E., Wu, B., Ottenheijm, C., Granzier, H. and Spencer, M.J. (2008) Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle. Hum. Mol. Genet., 17, 3271-3280.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3271-3280
-
-
Kramerova, I.1
Kudryashova, E.2
Wu, B.3
Ottenheijm, C.4
Granzier, H.5
Spencer, M.J.6
-
9
-
-
0000728204
-
The sarcoplasmic reticulum and the transverse tubules
-
Engel, A.G. and Franzini-Armstrong, C. (eds), McGraw-Hill, Inc., New York
-
Franzini-Armstrong, C. (1994) The sarcoplasmic reticulum and the transverse tubules. In Engel, A.G. and Franzini-Armstrong, C. (eds), Myology. McGraw-Hill, Inc., New York, Vol. 1, pp. 176-199.
-
(1994)
Myology
, vol.1
, pp. 176-199
-
-
Franzini-Armstrong, C.1
-
10
-
-
84872877697
-
Alteration of sarcoplasmic reticulum Ca release in skeletal muscle from calpain 3-deficient mice
-
Dayanithi, G., Richard, I., Viero, C., Mazuc, E., Mallie, S., Valmier, J., Bourg, N., Herasse, M., Marty, I., Lefranc, G. et al. (2009) Alteration of sarcoplasmic reticulum Ca release in skeletal muscle from calpain 3-deficient mice. Int. J. Cell Biol., 2009, 340346.
-
(2009)
Int. J. Cell Biol.
, vol.2009
, pp. 340346
-
-
Dayanithi, G.1
Richard, I.2
Viero, C.3
Mazuc, E.4
Mallie, S.5
Valmier, J.6
Bourg, N.7
Herasse, M.8
Marty, I.9
Lefranc, G.10
-
11
-
-
79952451731
-
Non-proteolytic functions of calpain-3 in sarcoplasmic reticulum in skeletal muscles
-
Ojima, K., Ono, Y., Ottenheijm, C., Hata, S., Suzuki, H., Granzier, H. and Sorimachi, H. (2011) Non-proteolytic functions of calpain-3 in sarcoplasmic reticulum in skeletal muscles. J. Mol. Biol., 407, 439-449.
-
(2011)
J. Mol. Biol.
, vol.407
, pp. 439-449
-
-
Ojima, K.1
Ono, Y.2
Ottenheijm, C.3
Hata, S.4
Suzuki, H.5
Granzier, H.6
Sorimachi, H.7
-
12
-
-
2942720949
-
The role of calcium and calcium/calmodulin-dependent kinases in skeletal muscle plasticity and mitochondrial biogenesis
-
Chin, E.R. (2004) The role of calcium and calcium/calmodulin-dependent kinases in skeletal muscle plasticity and mitochondrial biogenesis. Proc. Nutr. Soc., 63, 279-286.
-
(2004)
Proc. Nutr. Soc.
, vol.63
, pp. 279-286
-
-
Chin, E.R.1
-
13
-
-
33746328957
-
Signaling pathways in skeletal muscle remodeling
-
Bassel-Duby, R. and Olson, E.N. (2006) Signaling pathways in skeletal muscle remodeling. Ann. Rev. Biochem., 75, 19-37.
-
(2006)
Ann. Rev. Biochem.
, vol.75
, pp. 19-37
-
-
Bassel-Duby, R.1
Olson, E.N.2
-
14
-
-
0024443063
-
Studies of the regulatory mechanism of Ca2+/calmodulin-dependent protein kinase II
-
Fong, Y.L., Taylor, W.L., Means, A.R. and Soderling, T.R. (1989) Studies of the regulatory mechanism of Ca2+/calmodulin-dependent protein kinase II. Mutation of threonine 286 to alanine and aspartate. J. Biol. Chem., 264, 16759-16763.
-
(1989)
Mutation of threonine 286 to alanine and aspartate. J. Biol. Chem.
, vol.264
, pp. 16759-16763
-
-
Fong, Y.L.1
Taylor, W.L.2
Means, A.R.3
Soderling, T.R.4
-
15
-
-
23044495913
-
Role of Ca2+/calmodulin-dependent kinases in skeletal muscle plasticity
-
Chin, E.R. (2005) Role of Ca2+/calmodulin-dependent kinases in skeletal muscle plasticity. J. Appl. Physiol., 99, 414-423.
-
(2005)
J. Appl. Physiol.
, vol.99
, pp. 414-423
-
-
Chin, E.R.1
-
16
-
-
34848858523
-
Histone deacetylase degradation and MEF2 activation promote the formation of slow-twitch myofibers
-
Potthoff, M.J., Wu, H., Arnold, M.A., Shelton, J.M., Backs, J., McAnally, J., Richardson, J.A., Bassel-Duby, R. and Olson, E.N. (2007) Histone deacetylase degradation and MEF2 activation promote the formation of slow-twitch myofibers. J. Clin. Invest., 117, 2459-2467.
-
(2007)
J. Clin. Invest.
, vol.117
, pp. 2459-2467
-
-
Potthoff, M.J.1
Wu, H.2
Arnold, M.A.3
Shelton, J.M.4
Backs, J.5
McAnally, J.6
Richardson, J.A.7
Bassel-Duby, R.8
Olson, E.N.9
-
17
-
-
80051703420
-
Pathogenity of some limb girdle muscular dystrophy mutations can result from reduced anchorage to myofibrils and altered stability of calpain 3
-
Ermolova, N., Kudryashova, E., DiFranco, M., Vergara, J., Kramerova, I. and Spencer, M.J. (2011) Pathogenity of some limb girdle muscular dystrophy mutations can result from reduced anchorage to myofibrils and altered stability of calpain 3. Hum. Mol. Genet., 20, 3331-3345.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 3331-3345
-
-
Ermolova, N.1
Kudryashova, E.2
DiFranco, M.3
Vergara, J.4
Kramerova, I.5
Spencer, M.J.6
-
18
-
-
33847021853
-
Functional effects of mutations identified in patients with multiminicore disease
-
Zorzato, F., Jungbluth, H., Zhou, H., Muntoni, F. and Treves, S. (2007) Functional effects of mutations identified in patients with multiminicore disease. IUBMB Life, 59, 14-20.
-
(2007)
IUBMB Life
, vol.59
, pp. 14-20
-
-
Zorzato, F.1
Jungbluth, H.2
Zhou, H.3
Muntoni, F.4
Treves, S.5
-
19
-
-
34547757463
-
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
-
Zhou, H., Jungbluth, H., Sewry, C.A., Feng, L., Bertini, E., Bushby, K., Straub, V., Roper, H., Rose, M.R., Brockington, M. et al. (2007) Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies. Brain, 130, 2024-2036.
-
(2007)
Brain
, vol.130
, pp. 2024-2036
-
-
Zhou, H.1
Jungbluth, H.2
Sewry, C.A.3
Feng, L.4
Bertini, E.5
Bushby, K.6
Straub, V.7
Roper, H.8
Rose, M.R.9
Brockington, M.10
-
20
-
-
84864018328
-
-
Dubowitz, V. and Sewry, C.A. (2007) Muscle Biopsy: A Practical Approach. Sanders/Elsevier, Edinburgh.
-
(2007)
-
-
Dubowitz, V.1
Sewry, C.A.2
-
21
-
-
0027496090
-
Changes in myosin heavy chain isoform expression of overloaded rat skeletal muscles
-
Sugiura, T., Miyata, H., Kawai, Y., Matoba, H. and Murakami, N. (1993) Changes in myosin heavy chain isoform expression of overloaded rat skeletal muscles. Int. J. Biochem., 25, 1609-1613.
-
(1993)
Int. J. Biochem.
, vol.25
, pp. 1609-1613
-
-
Sugiura, T.1
Miyata, H.2
Kawai, Y.3
Matoba, H.4
Murakami, N.5
-
22
-
-
68749103451
-
Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle
-
Kramerova, I., Kudryashova, E., Wu, B., Germain, S., Vandenborne, K., Romain, N., Haller, R., Verity, M.A. and Spencer, M.J. (2009) Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle. Hum. Mol. Genet., 18, 3194-3205.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3194-3205
-
-
Kramerova, I.1
Kudryashova, E.2
Wu, B.3
Germain, S.4
Vandenborne, K.5
Romain, N.6
Haller, R.7
Verity, M.A.8
Spencer, M.J.9
-
23
-
-
33746735537
-
Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypes
-
Kho, A.T., Kang, P.B., Kohane, I.S. and Kunkel, L.M. (2006) Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypes. BMC Musculoskelet. Disord., 7, 23-31.
-
(2006)
BMC Musculoskelet. Disord.
, vol.7
, pp. 23-31
-
-
Kho, A.T.1
Kang, P.B.2
Kohane, I.S.3
Kunkel, L.M.4
-
24
-
-
0034019038
-
Myosin heavy chain isoform expression following reduced neuromuscular activity: potential regulatory mechanisms
-
Talmadge, R.J. (2000) Myosin heavy chain isoform expression following reduced neuromuscular activity: potential regulatory mechanisms. Muscle Nerve, 23, 661-679.
-
(2000)
Muscle Nerve
, vol.23
, pp. 661-679
-
-
Talmadge, R.J.1
-
25
-
-
17344390859
-
Skeletal muscle Ca(2+)-independent kinase activity increases during either hypertrophy or running
-
Fluck, M., Waxham, M.N., Hamilton, M.T. and Booth, F.W. (2000) Skeletal muscle Ca(2+)-independent kinase activity increases during either hypertrophy or running. J. Appl. Physiol., 88, 352-358.
-
(2000)
J. Appl. Physiol.
, vol.88
, pp. 352-358
-
-
Fluck, M.1
Waxham, M.N.2
Hamilton, M.T.3
Booth, F.W.4
-
26
-
-
0034640259
-
Three-dimensional reconstructions of calcium/calmodulin-dependent (CaM) kinase IIalpha and truncated CaM kinase IIalpha reveal a unique organization for its structural core and functional domains
-
Kolodziej, S.J., Hudmon, A., Waxham, M.N. and Stoops, J.K. (2000) Three-dimensional reconstructions of calcium/calmodulin-dependent (CaM) kinase IIalpha and truncated CaM kinase IIalpha reveal a unique organization for its structural core and functional domains. J. Biol. Chem., 275, 14354-14359.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 14354-14359
-
-
Kolodziej, S.J.1
Hudmon, A.2
Waxham, M.N.3
Stoops, J.K.4
-
27
-
-
0035830935
-
Cellular signaling through multifunctional Ca2+/calmodulin-dependent protein kinase II
-
Soderling, T.R., Chang, B. and Brickey, D. (2001) Cellular signaling through multifunctional Ca2+/calmodulin-dependent protein kinase II. J. Biol. Chem., 276, 3719-3722.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 3719-3722
-
-
Soderling, T.R.1
Chang, B.2
Brickey, D.3
-
28
-
-
26444610334
-
Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway
-
Kramerova, I., Kudryashova, E., Venkatraman, G. and Spencer, M.J. (2005) Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway. Hum. Mol. Genet., 14, 2125-2134.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2125-2134
-
-
Kramerova, I.1
Kudryashova, E.2
Venkatraman, G.3
Spencer, M.J.4
-
29
-
-
77952650308
-
CaMKII regulates contraction- but not insulin-induced glucose uptake in mouse skeletal muscle
-
Witczak, C.A., Jessen, N., Warro, D.M., Toyoda, T., Fujii, N., Anderson, M.E., Hirshman, M.F. and Goodyear, L.J. (2010) CaMKII regulates contraction- but not insulin-induced glucose uptake in mouse skeletal muscle. Am. J. Physiol. Endocrinol. Metab., 298, E1150-E1160.
-
(2010)
Am. J. Physiol. Endocrinol. Metab.
, vol.298
-
-
Witczak, C.A.1
Jessen, N.2
Warro, D.M.3
Toyoda, T.4
Fujii, N.5
Anderson, M.E.6
Hirshman, M.F.7
Goodyear, L.J.8
-
30
-
-
0034893933
-
Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy
-
Chae, J., Minami, N., Jin, Y., Nakagawa, M., Murayama, K., Igarashi, F. and Nonaka, I. (2001) Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy. Neuromus. Dis., 11, 547-555.
-
(2001)
Neuromus. Dis.
, vol.11
, pp. 547-555
-
-
Chae, J.1
Minami, N.2
Jin, Y.3
Nakagawa, M.4
Murayama, K.5
Igarashi, F.6
Nonaka, I.7
-
31
-
-
0029963979
-
Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island
-
Fardeau, M., Hillaire, D., Mignard, C., Feingold, N., Feingold, J., Mignard, D., de Ubeda, B., Collin, H., Tome, F.M., Richard, I. et al. (1996) Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island. Brain, 119, 295-308.
-
(1996)
Brain
, vol.119
, pp. 295-308
-
-
Fardeau, M.1
Hillaire, D.2
Mignard, C.3
Feingold, N.4
Feingold, J.5
Mignard, D.6
de Ubeda, B.7
Collin, H.8
Tome, F.M.9
Richard, I.10
-
32
-
-
33646176985
-
Targeted inhibition of Ca2+/calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle
-
Chakkalakal, J.V., Michel, S.A., Chin, E.R., Michel, R.N. and Jasmin, B.J. (2006) Targeted inhibition of Ca2+/calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle. Hum. Mol. Genet., 15, 1423-1435.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 1423-1435
-
-
Chakkalakal, J.V.1
Michel, S.A.2
Chin, E.R.3
Michel, R.N.4
Jasmin, B.J.5
-
33
-
-
33845596500
-
Peroxisome proliferatoractivated receptor gamma coactivator 1 coactivators, energy homeostasis, and metabolism
-
Handschin, C. and Spiegelman, B.M. (2006) Peroxisome proliferatoractivated receptor gamma coactivator 1 coactivators, energy homeostasis, and metabolism. Endocr. Rev., 27, 728-735.
-
(2006)
Endocr. Rev.
, vol.27
, pp. 728-735
-
-
Handschin, C.1
Spiegelman, B.M.2
-
34
-
-
0038810035
-
An autoregulatory loop controls peroxisome proliferator-activated receptor gamma coactivator 1alpha expression in muscle
-
Handschin, C., Rhee, J., Lin, J., Tarr, P.T. and Spiegelman, B.M. (2003) An autoregulatory loop controls peroxisome proliferator-activated receptor gamma coactivator 1alpha expression in muscle. Proc. Natl Acad. Sci. USA, 100, 7111-7116.
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 7111-7116
-
-
Handschin, C.1
Rhee, J.2
Lin, J.3
Tarr, P.T.4
Spiegelman, B.M.5
-
35
-
-
34147109662
-
PGC-1alpha regulates the neuromuscular junction program and ameliorates Duchenne muscular dystrophy
-
Handschin, C., Kobayashi, Y.M., Chin, S., Seale, P., Campbell, K.P. and Spiegelman, B.M. (2007) PGC-1alpha regulates the neuromuscular junction program and ameliorates Duchenne muscular dystrophy. Genes Dev., 21, 770-783.
-
(2007)
Genes Dev
, vol.21
, pp. 770-783
-
-
Handschin, C.1
Kobayashi, Y.M.2
Chin, S.3
Seale, P.4
Campbell, K.P.5
Spiegelman, B.M.6
-
36
-
-
0025169498
-
Isolation of transcriptionally active nuclei from striated muscle using Percoll density gradients
-
Hahn, C.G. and Covault, J. (1990) Isolation of transcriptionally active nuclei from striated muscle using Percoll density gradients. Anal. Biochem., 190, 193-197.
-
(1990)
Anal. Biochem.
, vol.190
, pp. 193-197
-
-
Hahn, C.G.1
Covault, J.2
-
37
-
-
33645291760
-
Trizol-based method for sample preparation and isoelectric focusing of halophilic proteins
-
Kirkland, P.A., Busby, J., Stevens, S. Jr. and Maupin-Furlow, J.A. (2006) Trizol-based method for sample preparation and isoelectric focusing of halophilic proteins. Anal. Biochem., 351, 254-259.
-
(2006)
Anal. Biochem.
, vol.351
, pp. 254-259
-
-
Kirkland, P.A.1
Busby, J.2
Stevens Jr., S.3
Maupin-Furlow, J.A.4
-
38
-
-
3242725958
-
Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro
-
Kramerova, I., Kudryashova, E., Tidball, J.G. and Spencer, M.J. (2004) Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro. Hum. Mol. Genet., 13, 1373-1388.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1373-1388
-
-
Kramerova, I.1
Kudryashova, E.2
Tidball, J.G.3
Spencer, M.J.4
-
39
-
-
56649091065
-
Gene expression profiling in limb-girdle muscular dystrophy 2A
-
Saenz, A., Azpitarte, M., Armananzas, R., Leturcq, F., Alzualde, A., Inza, I., Garcia-Bragado, F., De la Herran, G., Corcuera, J., Cabello, A. et al. (2008) Gene expression profiling in limb-girdle muscular dystrophy 2A. PLoS One, 3, e3750.
-
(2008)
PLoS One
, vol.3
-
-
Saenz, A.1
Azpitarte, M.2
Armananzas, R.3
Leturcq, F.4
Alzualde, A.5
Inza, I.6
Garcia-Bragado, F.7
De la Herran, G.8
Corcuera, J.9
Cabello, A.10
-
40
-
-
0036823748
-
A web-accessible complete transcriptome of normal human and DMD muscle
-
Bakay, M., Zhao, P., Chen, J. and Hoffman, E.P. (2002) A web-accessible complete transcriptome of normal human and DMD muscle. Neuromuscul. Disord., 12 (Suppl. 1), S125-S141.
-
(2002)
Neuromuscul. Disord.
, vol.12
, Issue.SUPPL. 1
-
-
Bakay, M.1
Zhao, P.2
Chen, J.3
Hoffman, E.P.4
-
41
-
-
0141568971
-
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
-
Haslett, J.N., Sanoudou, D., Kho, A.T., Han, M., Bennett, R.R., Kohane, I.S., Beggs, A.H. and Kunkel, L.M. (2003) Gene expression profiling of Duchenne muscular dystrophy skeletal muscle. Neurogenetics, 4, 163-171.
-
(2003)
Neurogenetics
, vol.4
, pp. 163-171
-
-
Haslett, J.N.1
Sanoudou, D.2
Kho, A.T.3
Han, M.4
Bennett, R.R.5
Kohane, I.S.6
Beggs, A.H.7
Kunkel, L.M.8
-
42
-
-
0002670572
-
The clinical examination of voluntary muscles
-
Walton, J.N. (ed.), Churchill Livingstone, Edinburgh, UK
-
Gardner-Medwin, D. and Walton, J.N. (1974) The clinical examination of voluntary muscles. In Walton, J.N. (ed.), Disorders of Voluntary Muscles. Churchill Livingstone, Edinburgh, UK, pp. 517-560.
-
(1974)
Disorders of Voluntary Muscles
, pp. 517-560
-
-
Gardner-Medwin, D.1
Walton, J.N.2
|