-
2
-
-
3242666915
-
Ventilatory support in facioscapulohumeral muscular dystrophy
-
Wohlgemuth M., van der Kooi E.L., van Kesteren R.G., van der Maarel S.M., and Padberg G.W. Ventilatory support in facioscapulohumeral muscular dystrophy. Neurology 63 (2004) 176-178
-
(2004)
Neurology
, vol.63
, pp. 176-178
-
-
Wohlgemuth, M.1
van der Kooi, E.L.2
van Kesteren, R.G.3
van der Maarel, S.M.4
Padberg, G.W.5
-
3
-
-
0023202070
-
Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy: a general association with genetic and therapeutic implications
-
Fitzsimons R.B., Gurwin E.B., and Bird A.C. Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy: a general association with genetic and therapeutic implications. Brain 110 (1987) 631-648
-
(1987)
Brain
, vol.110
, pp. 631-648
-
-
Fitzsimons, R.B.1
Gurwin, E.B.2
Bird, A.C.3
-
4
-
-
0028930856
-
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy
-
Padberg G.W., Brouwer O.F., de Keizer R.F., et al. On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy. Muscle Nerve (1995) S73-S80
-
(1995)
Muscle Nerve
-
-
Padberg, G.W.1
Brouwer, O.F.2
de Keizer, R.F.3
-
5
-
-
34250356405
-
Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child
-
Shields C.L., Zahler J., Falk N., et al. Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child. Arch Ophthalmol 125 (2007) 840-842
-
(2007)
Arch Ophthalmol
, vol.125
, pp. 840-842
-
-
Shields, C.L.1
Zahler, J.2
Falk, N.3
-
6
-
-
0031743597
-
Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy
-
Laforêt P., de Toma C., Eymard B., et al. Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy. Neurology 51 (1998) 1454-1456
-
(1998)
Neurology
, vol.51
, pp. 1454-1456
-
-
Laforêt, P.1
de Toma, C.2
Eymard, B.3
-
7
-
-
0026922062
-
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
-
Wijmenga C., Hewitt J.E., Sandkuijl L.A., et al. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nat Genet 2 (1992) 26-30
-
(1992)
Nat Genet
, vol.2
, pp. 26-30
-
-
Wijmenga, C.1
Hewitt, J.E.2
Sandkuijl, L.A.3
-
8
-
-
0029038951
-
Correlation between fragment size at D4F104S1 and age of onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD) [Erratum in: Hum Mol Genet 1995;4:1243-1244]
-
Lunt P.W., Jardine P.E., Koch M.C., et al. Correlation between fragment size at D4F104S1 and age of onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD) [Erratum in: Hum Mol Genet 1995;4:1243-1244]. Hum Mol Genet 4 (1995) 951-958
-
(1995)
Hum Mol Genet
, vol.4
, pp. 951-958
-
-
Lunt, P.W.1
Jardine, P.E.2
Koch, M.C.3
-
9
-
-
0029984970
-
Evidence for anticipation and association of deletion size with severity of facioscapulohumeral muscular dystrophy
-
The FSH-DY Group
-
Tawil R., Forrester J., Griggs R.C., et al., The FSH-DY Group. Evidence for anticipation and association of deletion size with severity of facioscapulohumeral muscular dystrophy. Ann Neurol 39 (1996) 744-748
-
(1996)
Ann Neurol
, vol.39
, pp. 744-748
-
-
Tawil, R.1
Forrester, J.2
Griggs, R.C.3
-
10
-
-
0030009384
-
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
-
Tupler R., Berardinelli A., Barbierato L., et al. Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy. J Med Genet 33 (1996) 366-370
-
(1996)
J Med Genet
, vol.33
, pp. 366-370
-
-
Tupler, R.1
Berardinelli, A.2
Barbierato, L.3
-
11
-
-
0029113034
-
The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes
-
Lyle R., Wright T.J., Clark L.N., and Hewitt J.E. The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes. Genomics 28 (1995) 389-397
-
(1995)
Genomics
, vol.28
, pp. 389-397
-
-
Lyle, R.1
Wright, T.J.2
Clark, L.N.3
Hewitt, J.E.4
-
12
-
-
0344436078
-
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
-
Gabriëls J., Beckers M.C., Ding H., et al. Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element. Gene 236 (1999) 25-32
-
(1999)
Gene
, vol.236
, pp. 25-32
-
-
Gabriëls, J.1
Beckers, M.C.2
Ding, H.3
-
13
-
-
0028040601
-
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy
-
Hewitt J.E., Lyle R., Clark L.N., et al. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hum Mol Genet 3 (1994) 1287-1295
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1287-1295
-
-
Hewitt, J.E.1
Lyle, R.2
Clark, L.N.3
-
14
-
-
34547754037
-
Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy
-
Clapp J., Mitchell L.M., Bolland D.J., et al. Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy. Am J Hum Genet 81 (2007) 264-279
-
(2007)
Am J Hum Genet
, vol.81
, pp. 264-279
-
-
Clapp, J.1
Mitchell, L.M.2
Bolland, D.J.3
-
15
-
-
9244232833
-
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35
-
van Deutekom J.C.T., Lemmers R.J.L.F., Grewal P.K., et al. Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35. Hum Mol Genet 5 (1996) 581-590
-
(1996)
Hum Mol Genet
, vol.5
, pp. 581-590
-
-
van Deutekom, J.C.T.1
Lemmers, R.J.L.F.2
Grewal, P.K.3
-
16
-
-
0032541318
-
FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates
-
Grewal P.K., Todd L.C., van der Maarel S., Frants R.R., and Hewitt J.E. FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates. Gene 216 (1998) 13-19
-
(1998)
Gene
, vol.216
, pp. 13-19
-
-
Grewal, P.K.1
Todd, L.C.2
van der Maarel, S.3
Frants, R.R.4
Hewitt, J.E.5
-
17
-
-
2342572330
-
FRG1P is localised in the nucleolus, Cajal bodies, and speckles
-
van Koningsbruggen S., Dirks R.W., Mommaas A.M., et al. FRG1P is localised in the nucleolus, Cajal bodies, and speckles. J Med Genet 41 (2004) e46
-
(2004)
J Med Genet
, vol.41
-
-
van Koningsbruggen, S.1
Dirks, R.W.2
Mommaas, A.M.3
-
18
-
-
0037047439
-
Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
Gabellini D., Green M., and Tupler R. Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell 110 (2002) 339-348
-
(2002)
Cell
, vol.110
, pp. 339-348
-
-
Gabellini, D.1
Green, M.2
Tupler, R.3
-
19
-
-
0345227304
-
Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q
-
Jiang G., Yang F., van Overveld P.G., Vedanarayanan V., van der Maarel S., and Ehrlich M. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q. Hum Mol Genet 12 (2003) 2909-2921
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2909-2921
-
-
Jiang, G.1
Yang, F.2
van Overveld, P.G.3
Vedanarayanan, V.4
van der Maarel, S.5
Ehrlich, M.6
-
20
-
-
0344875044
-
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
-
Winokur S.T., Chen Y.W., Masny P.S., et al. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Hum Mol Genet 12 (2003) 2895-2907
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2895-2907
-
-
Winokur, S.T.1
Chen, Y.W.2
Masny, P.S.3
-
21
-
-
33847234593
-
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
-
Osborne R.J., Welle S., Venance S.L., Thornton C.A., and Tawil R. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology 68 (2007) 569-577
-
(2007)
Neurology
, vol.68
, pp. 569-577
-
-
Osborne, R.J.1
Welle, S.2
Venance, S.L.3
Thornton, C.A.4
Tawil, R.5
-
22
-
-
4544273261
-
Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?
-
Masny P.S., Bengtsson U., Chung S.A., et al. Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?. Hum Mol Genet 13 (2004) 1857-1871
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1857-1871
-
-
Masny, P.S.1
Bengtsson, U.2
Chung, S.A.3
-
23
-
-
34548392207
-
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD
-
de Greef J.C., Wohlgemuth M., Chan O.A., et al. Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD. Neurology 69 (2007) 1018-1026
-
(2007)
Neurology
, vol.69
, pp. 1018-1026
-
-
de Greef, J.C.1
Wohlgemuth, M.2
Chan, O.A.3
-
24
-
-
38049094992
-
A nuclear matrix attachment site in the 4q35 locus has an enhancer-blocking activity in vivo: implications for the facio-scapulo-humeral dystrophy
-
Petrov A., Allinne J., Pirozhkova I., Laoudj D., Lipinski M., and Vassetzky Y.S. A nuclear matrix attachment site in the 4q35 locus has an enhancer-blocking activity in vivo: implications for the facio-scapulo-humeral dystrophy. Genome Res 18 (2008) 39-45
-
(2008)
Genome Res
, vol.18
, pp. 39-45
-
-
Petrov, A.1
Allinne, J.2
Pirozhkova, I.3
Laoudj, D.4
Lipinski, M.5
Vassetzky, Y.S.6
-
25
-
-
0032976224
-
Definitive molecular diagnosis of facioscapulohumeral dystrophy
-
Orrell R.W., Tawil R., Forrester J., Kissel J.T., Mendell J.R., and Figlewicz D.A. Definitive molecular diagnosis of facioscapulohumeral dystrophy. Neurology 52 (1999) 1822-1826
-
(1999)
Neurology
, vol.52
, pp. 1822-1826
-
-
Orrell, R.W.1
Tawil, R.2
Forrester, J.3
Kissel, J.T.4
Mendell, J.R.5
Figlewicz, D.A.6
-
26
-
-
0029827344
-
Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1
-
van Deutekom J.C., Bakker E., Lemmers R.J., et al. Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1. Hum Mol Genet 5 (1996) 1997-2003
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1997-2003
-
-
van Deutekom, J.C.1
Bakker, E.2
Lemmers, R.J.3
-
27
-
-
0032477313
-
Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports
-
Bushby K.M., Pollitt C., Johnson M.A., Rogers M.T., and Chinnery P.F. Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports. Neuromuscul Disord 8 (1998) 574-579
-
(1998)
Neuromuscul Disord
, vol.8
, pp. 574-579
-
-
Bushby, K.M.1
Pollitt, C.2
Johnson, M.A.3
Rogers, M.T.4
Chinnery, P.F.5
-
28
-
-
33745680948
-
Retinal vascular abnormalities in FSHD: a therapeutic message; clues to pathogenesis
-
Upadhyaya M., and Cooper D.N. (Eds), BIOS Scientific Publishers, New York
-
Fitzsimons R.B. Retinal vascular abnormalities in FSHD: a therapeutic message; clues to pathogenesis. In: Upadhyaya M., and Cooper D.N. (Eds). Facioscapulohumeral muscular dystrophy (FSHD): clinical medicine and molecular cell biology (2004), BIOS Scientific Publishers, New York 185-195
-
(2004)
Facioscapulohumeral muscular dystrophy (FSHD): clinical medicine and molecular cell biology
, pp. 185-195
-
-
Fitzsimons, R.B.1
-
29
-
-
0023763124
-
The effects of strength training in patients with selected neuromuscular disorders
-
McCartney N., Moroz D., Garner S.H., and McComas A.J. The effects of strength training in patients with selected neuromuscular disorders. Med Sci Sports Exerc 20 (1988) 362-368
-
(1988)
Med Sci Sports Exerc
, vol.20
, pp. 362-368
-
-
McCartney, N.1
Moroz, D.2
Garner, S.H.3
McComas, A.J.4
-
30
-
-
0023870777
-
Muscle strengthening through high-resistance weight training in patients with neuromuscular disorders
-
Milner-Brown H.S., and Miller R.G. Muscle strengthening through high-resistance weight training in patients with neuromuscular disorders. Arch Phys Med Rehabil 69 (1988) 14-19
-
(1988)
Arch Phys Med Rehabil
, vol.69
, pp. 14-19
-
-
Milner-Brown, H.S.1
Miller, R.G.2
-
31
-
-
0014013249
-
The effect of exercise in muscular dystrophy
-
Vignos Jr. P.J., and Watkins M.P. The effect of exercise in muscular dystrophy. JAMA 197 (1966) 843-848
-
(1966)
JAMA
, vol.197
, pp. 843-848
-
-
Vignos Jr., P.J.1
Watkins, M.P.2
-
32
-
-
15244356311
-
Aerobic training improves exercise performance in facioscapulohumeral muscular dystrophy
-
Olsen D.B., Ørngreen M.C., and Vissing J. Aerobic training improves exercise performance in facioscapulohumeral muscular dystrophy. Neurology 64 (2005) 1064-1066
-
(2005)
Neurology
, vol.64
, pp. 1064-1066
-
-
Olsen, D.B.1
Ørngreen, M.C.2
Vissing, J.3
-
33
-
-
4143138627
-
Strength training and albuterol in facioscapulohumeral muscular dystrophy
-
van der Kooi E.L., Vogels O.J., van Asseldonk R.J., et al. Strength training and albuterol in facioscapulohumeral muscular dystrophy. Neurology 63 (2004) 702-708
-
(2004)
Neurology
, vol.63
, pp. 702-708
-
-
van der Kooi, E.L.1
Vogels, O.J.2
van Asseldonk, R.J.3
-
34
-
-
0027195365
-
Scapulothoracic arthrodesis in facioscapulohumeral muscular dystrophy: review of seventeen procedures with three to twenty-one-year follow up
-
Bunch W.H., and Siegel I.M. Scapulothoracic arthrodesis in facioscapulohumeral muscular dystrophy: review of seventeen procedures with three to twenty-one-year follow up. J Bone Joint Surg Am 75 (1993) 372-376
-
(1993)
J Bone Joint Surg Am
, vol.75
, pp. 372-376
-
-
Bunch, W.H.1
Siegel, I.M.2
-
36
-
-
38949086661
-
Fixation of winged scapula in facioscapulohumeral muscular dystrophy
-
Giannini S., Faldini C., Pagkrati S., et al. Fixation of winged scapula in facioscapulohumeral muscular dystrophy. Clin Med Res 5 (2007) 155-162
-
(2007)
Clin Med Res
, vol.5
, pp. 155-162
-
-
Giannini, S.1
Faldini, C.2
Pagkrati, S.3
-
37
-
-
33745746655
-
Long-term results of scapulothoracic arthrodesis of facioscapulohumeral muscular dystrophy
-
Rhee Y.G., and Ha J.H. Long-term results of scapulothoracic arthrodesis of facioscapulohumeral muscular dystrophy. J Shoulder Elbow Surg 15 (2006) 445-450
-
(2006)
J Shoulder Elbow Surg
, vol.15
, pp. 445-450
-
-
Rhee, Y.G.1
Ha, J.H.2
-
39
-
-
13244295347
-
Brachial plexopathy following thoracoscapular fusion in facioscapulohumeral muscular dystrophy
-
Wolfe G.I., Young P.K., Nations S.P., Burkhead W.Z., McVey A.L., and Barohn R.J. Brachial plexopathy following thoracoscapular fusion in facioscapulohumeral muscular dystrophy. Neurology 64 (2005) 572-573
-
(2005)
Neurology
, vol.64
, pp. 572-573
-
-
Wolfe, G.I.1
Young, P.K.2
Nations, S.P.3
Burkhead, W.Z.4
McVey, A.L.5
Barohn, R.J.6
-
41
-
-
0030794634
-
Use of gold weights to correct lagophthalmos in neuromuscular disease
-
Sansone V., Boynton J., and Palenski C. Use of gold weights to correct lagophthalmos in neuromuscular disease. Neurology 48 (1997) 1500-1503
-
(1997)
Neurology
, vol.48
, pp. 1500-1503
-
-
Sansone, V.1
Boynton, J.2
Palenski, C.3
-
42
-
-
0015323857
-
Inflammatory myopathy with facioscapulohumeral distribution
-
Munsat T.L., Piper D., Cancilla P., and Mednick J. Inflammatory myopathy with facioscapulohumeral distribution. Neurology 22 (1972) 335-347
-
(1972)
Neurology
, vol.22
, pp. 335-347
-
-
Munsat, T.L.1
Piper, D.2
Cancilla, P.3
Mednick, J.4
-
43
-
-
0015786604
-
"Polymyositis" with involvement of facial and distal musculature: one form of the facioscapulohumeral syndrome?
-
Bates D., Stevens J.C., and Hudgson P. "Polymyositis" with involvement of facial and distal musculature: one form of the facioscapulohumeral syndrome?. J Neurol Sci 19 (1973) 105-108
-
(1973)
J Neurol Sci
, vol.19
, pp. 105-108
-
-
Bates, D.1
Stevens, J.C.2
Hudgson, P.3
-
44
-
-
0019979615
-
Inflammatory facioscapulohumeral muscular dystrophy and Coats syndrome
-
Wulff J.D., Lin J.T., and Kepes J.J. Inflammatory facioscapulohumeral muscular dystrophy and Coats syndrome. Ann Neurol 12 (1982) 398-401
-
(1982)
Ann Neurol
, vol.12
, pp. 398-401
-
-
Wulff, J.D.1
Lin, J.T.2
Kepes, J.J.3
-
45
-
-
0031031974
-
A pilot study of prednisone in facioscapulohumeral muscular dystrophy
-
The FSH-DY Group
-
Tawil R., McDermott M.P., Pandya S., et al., The FSH-DY Group. A pilot study of prednisone in facioscapulohumeral muscular dystrophy. Neurology 48 (1997) 46-49
-
(1997)
Neurology
, vol.48
, pp. 46-49
-
-
Tawil, R.1
McDermott, M.P.2
Pandya, S.3
-
46
-
-
0025777405
-
Decreased myofibrillar protein breakdown following treatment with clenbuterol
-
Benson D.W., Foley-Nelson T., Chance W.T., Zhang F.S., James J.H., and Fischer J.E. Decreased myofibrillar protein breakdown following treatment with clenbuterol. J Surg Res 50 (1991) 1-5
-
(1991)
J Surg Res
, vol.50
, pp. 1-5
-
-
Benson, D.W.1
Foley-Nelson, T.2
Chance, W.T.3
Zhang, F.S.4
James, J.H.5
Fischer, J.E.6
-
47
-
-
0027027228
-
Tissue specific responses to clenbuterol; temporal changes in protein metabolism of striated muscle and visceral tissues from rats
-
Matlin C.A., Hay S.M., McMillan D.N., and Delday M.I. Tissue specific responses to clenbuterol; temporal changes in protein metabolism of striated muscle and visceral tissues from rats. Growth Regul 2 (1992) 161-166
-
(1992)
Growth Regul
, vol.2
, pp. 161-166
-
-
Matlin, C.A.1
Hay, S.M.2
McMillan, D.N.3
Delday, M.I.4
-
48
-
-
0026568326
-
Effect of clenbuterol on skeletal muscle atrophy in mice induced by the glucocorticoid dexamethasone
-
Agbenyega E.T., and Wareham A.C. Effect of clenbuterol on skeletal muscle atrophy in mice induced by the glucocorticoid dexamethasone. Comp Biochem Physiol Comp Physiol 102 (1992) 141-145
-
(1992)
Comp Biochem Physiol Comp Physiol
, vol.102
, pp. 141-145
-
-
Agbenyega, E.T.1
Wareham, A.C.2
-
49
-
-
0024433181
-
Muscle wasting associated with endotoxemia in the rat: modification by the β2-adrenoceptor agonist clenbuterol
-
Choo J.J., Horan M.A., Little R.A., and Rothwell N.J. Muscle wasting associated with endotoxemia in the rat: modification by the β2-adrenoceptor agonist clenbuterol. Biosci Rep 9 (1989) 615-621
-
(1989)
Biosci Rep
, vol.9
, pp. 615-621
-
-
Choo, J.J.1
Horan, M.A.2
Little, R.A.3
Rothwell, N.J.4
-
50
-
-
0032493104
-
Examining the potential drug therapies for muscular dystrophy utilising the dy/dy mouse: I. Clenbuterol
-
Hayes A., and Williams D.A. Examining the potential drug therapies for muscular dystrophy utilising the dy/dy mouse: I. Clenbuterol. J Neurol Sci 157 (1998) 122-128
-
(1998)
J Neurol Sci
, vol.157
, pp. 122-128
-
-
Hayes, A.1
Williams, D.A.2
-
51
-
-
0023178857
-
Clenbuterol, a β2 agonist, retards atrophy in denervated muscles
-
Zeman R.J., Ludemann R., and Etlinger J.D. Clenbuterol, a β2 agonist, retards atrophy in denervated muscles. Am J Physiol 252 (1987) E152-E155
-
(1987)
Am J Physiol
, vol.252
-
-
Zeman, R.J.1
Ludemann, R.2
Etlinger, J.D.3
-
52
-
-
0026452918
-
Salbutamol, a β2-adrenoceptor agonist, increases skeletal muscle strength in young men [Erratum in: Clin Sci 1993;84(6):following XX]
-
Martineau L., Horan M.A., Rothwell N.J., and Little R.A. Salbutamol, a β2-adrenoceptor agonist, increases skeletal muscle strength in young men [Erratum in: Clin Sci 1993;84(6):following XX]. Clin Sci (Lond) 83 (1992) 615-621
-
(1992)
Clin Sci (Lond)
, vol.83
, pp. 615-621
-
-
Martineau, L.1
Horan, M.A.2
Rothwell, N.J.3
Little, R.A.4
-
53
-
-
0035940617
-
Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral muscular dystrophy
-
The FSH-DY Group
-
Kissel J.T., McDermott M.P., Mendell J.R., et al., The FSH-DY Group. Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral muscular dystrophy. Neurology 57 (2001) 1434-1440
-
(2001)
Neurology
, vol.57
, pp. 1434-1440
-
-
Kissel, J.T.1
McDermott, M.P.2
Mendell, J.R.3
-
54
-
-
0027285526
-
Cellular energetics of dystrophic muscle
-
Kemp G.J., Taylor D.J., Dunn J.F., Frostick S.P., and Radda G.K. Cellular energetics of dystrophic muscle. J Neurol Sci 116 (1993) 201-206
-
(1993)
J Neurol Sci
, vol.116
, pp. 201-206
-
-
Kemp, G.J.1
Taylor, D.J.2
Dunn, J.F.3
Frostick, S.P.4
Radda, G.K.5
-
56
-
-
0343022262
-
Creatine monohydrate in muscular dystrophies: a double-blind placebo controlled clinical study
-
Walter M.C., Lochmüller H., Reilich P., et al. Creatine monohydrate in muscular dystrophies: a double-blind placebo controlled clinical study. Neurology 54 (2000) 1848-1850
-
(2000)
Neurology
, vol.54
, pp. 1848-1850
-
-
Walter, M.C.1
Lochmüller, H.2
Reilich, P.3
-
57
-
-
3843080877
-
Drug treatment for facioscapulohumeral muscular dystrophy
-
CD002276
-
Rose M.R., and Tawil R. Drug treatment for facioscapulohumeral muscular dystrophy. Cochrane Database Syst Rev 2 (2004) CD002276
-
(2004)
Cochrane Database Syst Rev
, Issue.2
-
-
Rose, M.R.1
Tawil, R.2
-
58
-
-
13444293017
-
The function of myostatin and strategies of myostatin blockade: new hope for therapies aimed at promoting growth of skeletal muscle
-
Patel K., and Amthor H. The function of myostatin and strategies of myostatin blockade: new hope for therapies aimed at promoting growth of skeletal muscle. Neuromuscul Disord 15 (2005) 117-126
-
(2005)
Neuromuscul Disord
, vol.15
, pp. 117-126
-
-
Patel, K.1
Amthor, H.2
-
59
-
-
44849140764
-
A phase I/II trial of MYO-029 in adult subjects with muscular dystrophy
-
Wagner K.R., Fleckenstein J.L., Amato A.A., et al. A phase I/II trial of MYO-029 in adult subjects with muscular dystrophy. Ann Neurol 63 (2008) 561-571
-
(2008)
Ann Neurol
, vol.63
, pp. 561-571
-
-
Wagner, K.R.1
Fleckenstein, J.L.2
Amato, A.A.3
-
60
-
-
25444435141
-
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy
-
van Overveld P.G., Enthoven L., Ricci E., et al. Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy. Ann Neurol 58 (2005) 569-576
-
(2005)
Ann Neurol
, vol.58
, pp. 569-576
-
-
van Overveld, P.G.1
Enthoven, L.2
Ricci, E.3
-
61
-
-
33750488776
-
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy
-
van der Kooi E.L., de Greef J.C., Wohlgemuth M., et al. No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy. Neuromuscul Disord 16 (2006) 766-769
-
(2006)
Neuromuscul Disord
, vol.16
, pp. 766-769
-
-
van der Kooi, E.L.1
de Greef, J.C.2
Wohlgemuth, M.3
-
62
-
-
29144466479
-
Regulation of muscle growth by multiple ligands signaling through activin type II receptors
-
Lee S.J., Reed L.A., Davies M.V., et al. Regulation of muscle growth by multiple ligands signaling through activin type II receptors. Proc Natl Acad Sci U S A 102 (2005) 18117-18122
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 18117-18122
-
-
Lee, S.J.1
Reed, L.A.2
Davies, M.V.3
-
63
-
-
53049083486
-
Novel myostatin inhibitors increase muscle mass in wild-type and mdx mice
-
abstract
-
Lachey J., Pullen A., Pearsall R., and Seehra J. Novel myostatin inhibitors increase muscle mass in wild-type and mdx mice. Neuromuscul Disord 17 (2007) 785 abstract
-
(2007)
Neuromuscul Disord
, vol.17
, pp. 785
-
-
Lachey, J.1
Pullen, A.2
Pearsall, R.3
Seehra, J.4
-
64
-
-
27944486698
-
Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients
-
Vilquin J.T., Marolleau J.P., Sacconi S., et al. Normal growth and regenerating ability of myoblasts from unaffected muscles of facioscapulohumeral muscular dystrophy patients. Gene Ther 12 (2005) 1651-1662
-
(2005)
Gene Ther
, vol.12
, pp. 1651-1662
-
-
Vilquin, J.T.1
Marolleau, J.P.2
Sacconi, S.3
-
65
-
-
37349061115
-
Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies
-
Morosetti R., Mirabella M., Gliubizzi C., et al. Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies. Stem Cells 25 (2007) 3173-3182
-
(2007)
Stem Cells
, vol.25
, pp. 3173-3182
-
-
Morosetti, R.1
Mirabella, M.2
Gliubizzi, C.3
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