-
1
-
-
84924923845
-
Myopathy due to a defect in muscle glycogen breakdown
-
Mc Ardle B. Myopathy due to a defect in muscle glycogen breakdown. Clin Sci 1951;10:13-36.
-
(1951)
Clin Sci
, vol.10
, pp. 13-36
-
-
Mc Ardle, B.1
-
3
-
-
0003038372
-
Metabolic myopathies
-
Vinken PJ, Bruyn GW, Ringel SP, editors. Amsterdam: North Holand
-
DiMauro S. Metabolic myopathies. In: Vinken PJ, Bruyn GW, Ringel SP, editors. Handbook of Clinical Neurology. Amsterdam: North Holand; 1978. p. 175-234.
-
(1978)
Handbook of Clinical Neurology
, pp. 175-234
-
-
DiMauro, S.1
-
4
-
-
85030939535
-
Glycogénoses musculaires
-
17180 A10, 4-1984, 18 p.
-
Pellissier JF, De Barsy T., Toga M. Glycogénoses musculaires. - Encycl. Méd. Chir., (Paris, France), Neurologie, 17180 A10, 4-1984, 18 p.
-
Encycl. Méd. Chir., (Paris, France), Neurologie
-
-
Pellissier, J.F.1
De Barsy, T.2
Toga, M.3
-
5
-
-
0018086688
-
Fatal infantile form of muscle phosphorylase deficiency
-
DiMauro S, Hartlage PL. Fatal infantile form of muscle phosphorylase deficiency. Neurology 1978;28:1124-9.
-
(1978)
Neurology
, vol.28
, pp. 1124-1129
-
-
DiMauro, S.1
Hartlage, P.L.2
-
7
-
-
0026352029
-
Une autre étiologie de la claudication intermittente des mâchoires: La maladie de Mac Ardle (glycogénose musculaire de type V)
-
Dupond JL, Maire I, De Wazieres B, Billerey C, Morin G, Desmurs H. Une autre étiologie de la claudication intermittente des mâchoires: la maladie de Mac Ardle (glycogénose musculaire de type V). Ann Med Interne 1991;142(7):556-7.
-
(1991)
Ann Med Interne
, vol.142
, Issue.7
, pp. 556-557
-
-
Dupond, J.L.1
Maire, I.2
De Wazieres, B.3
Billerey, C.4
Morin, G.5
Desmurs, H.6
-
8
-
-
0030973265
-
État dépressif, rhabdomyolyse et syndrome inflammatoire chez un patient de 71 ans
-
Colin JY, Coquet M, Ghit K, Mottaz P. État dépressif, rhabdomyolyse et syndrome inflammatoire chez un patient de 71 ans. Rev Med Interne 1997;18(Suppl 3):303-4.
-
(1997)
Rev Med Interne
, vol.18
, Issue.SUPPL. 3
, pp. 303-304
-
-
Colin, J.Y.1
Coquet, M.2
Ghit, K.3
Mottaz, P.4
-
9
-
-
0032900071
-
Late-onset McArdle's disease mimicking treatment-resistant polymyositis. Report of a case and review of the literature
-
Pego R, Gonzalez-Gay MA, Garcia-Porrua C, Branas F, Navarro C. Late-onset McArdle's disease mimicking treatment-resistant polymyositis. Report of a case and review of the literature. Rev Rhum Engl Ed 1999;66:236-7.
-
(1999)
Rev Rhum Engl Ed
, vol.66
, pp. 236-237
-
-
Pego, R.1
Gonzalez-Gay, M.A.2
Garcia-Porrua, C.3
Branas, F.4
Navarro, C.5
-
10
-
-
0034028548
-
McArdle's disease presenting with asymmetric, late-onset arm weakness
-
Wolfe GI, Baker NS, Haller RG, Bums DK, Barohm RJ. McArdle's disease presenting with asymmetric, late-onset arm weakness. Muscle Nerve 2000;23:641-5.
-
(2000)
Muscle Nerve
, vol.23
, pp. 641-645
-
-
Wolfe, G.I.1
Baker, N.S.2
Haller, R.G.3
Bums, D.K.4
Barohm, R.J.5
-
11
-
-
0021966688
-
McArdle's disease in an elderly woman
-
Harris RA, Dowben RM. McArdle's disease in an elderly woman. South Med J 1985;78:191-3.
-
(1985)
South Med J
, vol.78
, pp. 191-193
-
-
Harris, R.A.1
Dowben, R.M.2
-
13
-
-
0022973083
-
The second wind phenomenon in McArdle's disease
-
Braakhekke JP, de Bruin MI, Stegeman DF, Wevers RA, Binkhorst RA, Joosten EM. The second wind phenomenon in McArdle's disease. Brain 1986;109:1087-101.
-
(1986)
Brain
, vol.109
, pp. 1087-1101
-
-
Braakhekke, J.P.1
De Bruin, M.I.2
Stegeman, D.F.3
Wevers, R.A.4
Binkhorst, R.A.5
Joosten, E.M.6
-
14
-
-
0035041025
-
ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle's disease
-
Lofberg M, Lindholm H, Naveri H, Majander A, Suomalainen A, Paetau A, et al. ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle's disease. Neuromuscul Disord 2001;11:370-5.
-
(2001)
Neuromuscul Disord
, vol.11
, pp. 370-375
-
-
Lofberg, M.1
Lindholm, H.2
Naveri, H.3
Majander, A.4
Suomalainen, A.5
Paetau, A.6
-
15
-
-
0016784092
-
McArdle's disease: A review
-
Lubran MM. McArdle's disease: a review. Ann Clin Lab Sci 1975;5:115-22.
-
(1975)
Ann Clin Lab Sci
, vol.5
, pp. 115-122
-
-
Lubran, M.M.1
-
17
-
-
0011228610
-
Late-onset type of skeletal muscle phosphorylase deficiency. A new familial variety with completely and partially affected subjects
-
Engel WK, Eyerman EL, Williams HE. Late-onset type of skeletal muscle phosphorylase deficiency. A new familial variety with completely and partially affected subjects. N Eng J Med 1963;268:135-7.
-
(1963)
N Eng J Med
, vol.268
, pp. 135-137
-
-
Engel, W.K.1
Eyerman, E.L.2
Williams, H.E.3
-
18
-
-
0018423953
-
Debranche deficiency: Neuromuscular disorder in 5 adults
-
Di Mauro S, Hartwig GB, Hays A, Eastwood A, Franco R, Olarte M, et al. Debranche deficiency: neuromuscular disorder in 5 adults. Ann Neurol 1979;5:422-36.
-
(1979)
Ann Neurol
, vol.5
, pp. 422-436
-
-
Di Mauro, S.1
Hartwig, G.B.2
Hays, A.3
Eastwood, A.4
Franco, R.5
Olarte, M.6
-
19
-
-
0035954322
-
A non-ischemic test for screening of patients with exercise intolerance
-
Hogrel JY, Laforet P, Ben Yaou R, Chevrot M, Eymard B, Lombes A. A non-ischemic test for screening of patients with exercise intolerance. Neurology 2001;56:1733-8.
-
(2001)
Neurology
, vol.56
, pp. 1733-1738
-
-
Hogrel, J.Y.1
Laforet, P.2
Ben Yaou, R.3
Chevrot, M.4
Eymard, B.5
Lombes, A.6
-
20
-
-
0036327398
-
-
Kazemi-Esfarjani P, Skomorowska E, Jensen TD, Haller RG, Vissing J. Ann Neurol 2002;52:153-9.
-
(2002)
Ann Neurol
, vol.52
, pp. 153-159
-
-
Kazemi-Esfarjani, P.1
Skomorowska, E.2
Jensen, T.D.3
Haller, R.G.4
Vissing, J.5
-
21
-
-
0034089669
-
Congenital and metabolic myopathies of childhood or adult onset
-
Miro O, Laguno M, Masanes F, Perea M, Urbano-Marquez A, Grau JM. Congenital and metabolic myopathies of childhood or adult onset. Semin Arthritis Rheum 2000;29:335-47.
-
(2000)
Semin Arthritis Rheum
, vol.29
, pp. 335-347
-
-
Miro, O.1
Laguno, M.2
Masanes, F.3
Perea, M.4
Urbano-Marquez, A.5
Grau, J.M.6
-
22
-
-
0014041429
-
An electromyographic diagnostic screening test in McArdle's disease and a case report
-
Dyken ML, Smith DM, Peake RL. An electromyographic diagnostic screening test in McArdle's disease and a case report. Neurology 1967;17:45-50.
-
(1967)
Neurology
, vol.17
, pp. 45-50
-
-
Dyken, M.L.1
Smith, D.M.2
Peake, R.L.3
-
23
-
-
0020630541
-
Late-onset McArdle's disease with unusual electromyographic findings
-
Pourmand R, Sanders DB, Corwin HM. Late-onset Mc Ardle's disease with unusual electromyographic findings. Arch Neurol 1983;40:374-7.
-
(1983)
Arch Neurol
, vol.40
, pp. 374-377
-
-
Pourmand, R.1
Sanders, D.B.2
Corwin, H.M.3
-
24
-
-
0024805328
-
McArdle's disease presenting as treatment resistant polymyositis
-
Higgs JB, Blaivas M, Albers JW. McArdle's disease presenting as treatment resistant polymyositis. J Rheumatol 1989:161588-91.
-
(1989)
J Rheumatol
, pp. 161588-161591
-
-
Higgs, J.B.1
Blaivas, M.2
Albers, J.W.3
-
25
-
-
0014051789
-
À propos d'une nouvelle observation d'absence de phosphorylase dans le muscle strié (maladie de Mac Ardle)
-
Delwaide PJ, Reznik M, Lemaire R, Lelievre P, Bonnet F. À propos d'une nouvelle observation d'absence de phosphorylase dans le muscle strié (maladie de Mac Ardle). Rev Neurol 1967;116:119-40.
-
(1967)
Rev Neurol
, vol.116
, pp. 119-140
-
-
Delwaide, P.J.1
Reznik, M.2
Lemaire, R.3
Lelievre, P.4
Bonnet, F.5
-
26
-
-
0242673503
-
McArdle's disease. Report of the first case in japan and its electromyographic and histological studies
-
Yasuto I, Tetsuji S, Hiroshi S. McArdle's disease. Report of the first case in japan and its electromyographic and histological studies. Clin Neurol 1975;15:457.
-
(1975)
Clin Neurol
, vol.15
, pp. 457
-
-
Yasuto, I.1
Tetsuji, S.2
Hiroshi, S.3
|