-
1
-
-
0001154148
-
Nonlysosomal glycogenoses
-
Engel AG, Franzini-Armstrong C (eds): New York, McGraw-Hill
-
DiMauro S, Tsujino S: Nonlysosomal glycogenoses, in Engel AG, Franzini-Armstrong C (eds): Myology, 2nd ed, vol 2. New York, McGraw-Hill, 1994, pp 1554-1576.
-
(1994)
Myology, 2nd Ed
, vol.2
, pp. 1554-1576
-
-
DiMauro, S.1
Tsujino, S.2
-
2
-
-
0026778353
-
Rhabdomyolysis in childhood. A primer on normal muscle function and selected myopathies characterized by disordered energy production
-
Brumback RA, Feeback DL, Leech RW: Rhabdomyolysis in childhood. A primer on normal muscle function and selected myopathies characterized by disordered energy production. Pediatr Clin North Am 1992;39:821-858.
-
(1992)
Pediatr Clin North Am
, vol.39
, pp. 821-858
-
-
Brumback, R.A.1
Feeback, D.L.2
Leech, R.W.3
-
3
-
-
0027194215
-
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)
-
Tsujino S, Shanske S, DiMauro S: Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease). N Engl J Med 1993;329:241-245.
-
(1993)
N Engl J Med
, vol.329
, pp. 241-245
-
-
Tsujino, S.1
Shanske, S.2
DiMauro, S.3
-
4
-
-
0031751198
-
Glycogen storage diseases of muscle
-
DiMauro S, Bruno C: Glycogen storage diseases of muscle. Curr Opin Neurol 1998;11:477-484.
-
(1998)
Curr Opin Neurol
, vol.11
, pp. 477-484
-
-
DiMauro, S.1
Bruno, C.2
-
5
-
-
0018423953
-
Debrancher deficiency: Neuromuscular disorder in five adults
-
DiMauro S, Hartwig GB, Hays AP, et al: Debrancher deficiency: Neuromuscular disorder in five adults. Ann Neurol 1979;5:422-436.
-
(1979)
Ann Neurol
, vol.5
, pp. 422-436
-
-
DiMauro, S.1
Hartwig, G.B.2
Hays, A.P.3
-
6
-
-
0031940193
-
Mutation analysis in myophosphorylase deficiency (McArdle's disease)
-
Vorgerd M, Kubish C, Burwinkel B, et al: Mutation analysis in myophosphorylase deficiency (McArdle's disease). Ann Neurol 1998;43:326-331.
-
(1998)
Ann Neurol
, vol.43
, pp. 326-331
-
-
Vorgerd, M.1
Kubish, C.2
Burwinkel, B.3
-
7
-
-
0015914021
-
Pitfalls in interpreting serum creatine phosphokinase activity
-
Nevins MA, Sara M, Bright M, Lyon LJ: Pitfalls in interpreting serum creatine phosphokinase activity. JAMA 1973;224:1382-1387.
-
(1973)
JAMA
, vol.224
, pp. 1382-1387
-
-
Nevins, M.A.1
Sara, M.2
Bright, M.3
Lyon, L.J.4
-
8
-
-
0019169473
-
Creatine kinase in hyperlipoproteinemic patients treated with clofibrate
-
Schneider J, Muhfellner G, Kaffarnik H: Creatine kinase in hyperlipoproteinemic patients treated with clofibrate. Artery 1980;8:164-170.
-
(1980)
Artery
, vol.8
, pp. 164-170
-
-
Schneider, J.1
Muhfellner, G.2
Kaffarnik, H.3
-
9
-
-
0021349184
-
Unusual manifestations of hypothyroidism
-
Klein I, Lewey GS: Unusual manifestations of hypothyroidism. Arch Intern Med 1984;144:123-128.
-
(1984)
Arch Intern Med
, vol.144
, pp. 123-128
-
-
Klein, I.1
Lewey, G.S.2
-
11
-
-
0023845307
-
Persistent hyperCKemia: Fourteen patients studied in retrospect
-
Brewster LM, de Visser M: Persistent hyperCKemia: Fourteen patients studied in retrospect. Acta Neurol Scand 1988;77:60-63.
-
(1988)
Acta Neurol Scand
, vol.77
, pp. 60-63
-
-
Brewster, L.M.1
De Visser, M.2
-
12
-
-
0002656167
-
Approaches to the membrane theory of Duchenne muscular dystrophy
-
Angelini C, Danieli GA, Fontanari D (eds): Amsterdam, Excerpta Medica
-
Rowland LP, Willner J, Cerri C, et al: Approaches to the membrane theory of Duchenne muscular dystrophy, in Angelini C, Danieli GA, Fontanari D (eds): Muscular Dystrophy Research: Advances and New Trends. Amsterdam, Excerpta Medica, 1980, pp 3-13.
-
(1980)
Muscular Dystrophy Research: Advances and New Trends
, pp. 3-13
-
-
Rowland, L.P.1
Willner, J.2
Cerri, C.3
-
14
-
-
0023132925
-
High serum levels of creatine kinase: Asymptomatic prelude to distal myopathy
-
Galassi G, Rowland LP, Hays AP, et al: High serum levels of creatine kinase: Asymptomatic prelude to distal myopathy. Muscle Nerve 1987;10:346-350.
-
(1987)
Muscle Nerve
, vol.10
, pp. 346-350
-
-
Galassi, G.1
Rowland, L.P.2
Hays, A.P.3
-
15
-
-
0024544201
-
Asymptomatic hyper-CK-emia: An electrophysiologic and histopathologic study
-
Joy JL, Oh SJ: Asymptomatic hyper-CK-emia: An electrophysiologic and histopathologic study. Muscle Nerve 1989;12:206-209.
-
(1989)
Muscle Nerve
, vol.12
, pp. 206-209
-
-
Joy, J.L.1
Oh, S.J.2
-
16
-
-
0025127475
-
Asymptomatic hyperCKemia: Detection of an isolated carrier of Duchenne muscular dystrophy
-
Tachi N, Wakai S, Yutoh Y, et al: Asymptomatic hyperCKemia: Detection of an isolated carrier of Duchenne muscular dystrophy. J Child Neurol 1990;5:351-353.
-
(1990)
J Child Neurol
, vol.5
, pp. 351-353
-
-
Tachi, N.1
Wakai, S.2
Yutoh, Y.3
-
17
-
-
0025870190
-
Unexplained increases in serum creatine kinase levels: Its relation to malignant hyperthermia susceptibility
-
Lingaraju N, Rosenberg H: Unexplained increases in serum creatine kinase levels: Its relation to malignant hyperthermia susceptibility. Anesth Analg 1991;72:702-705.
-
(1991)
Anesth Analg
, vol.72
, pp. 702-705
-
-
Lingaraju, N.1
Rosenberg, H.2
-
18
-
-
0029159952
-
Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family
-
Frydman M, Straussberg R, Shomrat R, et al: Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family. Am J Med Genet 1995;58:209-212.
-
(1995)
Am J Med Genet
, vol.58
, pp. 209-212
-
-
Frydman, M.1
Straussberg, R.2
Shomrat, R.3
-
19
-
-
0030909759
-
Malignant hyperthermia testing in patients with persistently increased serum creatine kinase levels
-
Weglinski MR, Wedel DJ, Engel AG: Malignant hyperthermia testing in patients with persistently increased serum creatine kinase levels. Anesth Analg 1997;84:1038-1041.
-
(1997)
Anesth Analg
, vol.84
, pp. 1038-1041
-
-
Weglinski, M.R.1
Wedel, D.J.2
Engel, A.G.3
-
20
-
-
0031694106
-
Idiopathic hyperCKemia revisited, editorial
-
Afifi AK: Idiopathic hyperCKemia revisited, editorial. J Child Neurol 1998;13:251-252.
-
(1998)
J Child Neurol
, vol.13
, pp. 251-252
-
-
Afifi, A.K.1
-
21
-
-
0031666666
-
Asymptomatic McArdle's disease associated with hyperCKemia and absence of myophosphorylase
-
Gospe SM, El-Schahawi M, Shanske S, et al: Asymptomatic McArdle's disease associated with hyperCKemia and absence of myophosphorylase. Neurology 1998;51:1228-1229.
-
(1998)
Neurology
, vol.51
, pp. 1228-1229
-
-
Gospe, S.M.1
El-Schahawi, M.2
Shanske, S.3
|