SchaerH., SteinmannB., JerusalemS., MaierC.Rhabdomyolysis induced by anaesthesia with intraoperative cardiac arrest. Br J Anaesth1977; 49: 495–499.
9.
SeayA.R., ZiterF.A., ThompsonJ.A.Cardiac arrest during induction of anaesthesia in Duchenne muscular dystrophy. J Pediatrics1978; 93: 88–90.
10.
MillerE.D., SandersD.B., RowlinsonJ.C., BerryF.A., SussmanM.D., EpsteinR.M.Anaesthesia-induced rhabdomyolysis in a patient with Duchenne's muscular dystrophy. Anesthesiology1978; 48: 146–148.
11.
LinterS.P.K., ThomasP.R., WithingtonP.S., HallM.G.Suxamethonium associated hypertonicity and cardiac arrest in unsuspected pesudohypertrophic muscular dystrophy. Br J Anaesth1982; 54: 1331–1332.
12.
McKishnieJ.D., GirvanD.P.Anaesthesia induced rhabdomyolysis. Can Anaesth Soc J1983; 30: 295–298.
13.
HendersonW.A.V.Succinylcholine induced cardiac arrest in unsuspected Duchenne muscular dystrophy. Can Anaesth Soc J1984; 31: 444–446.
14.
RubianoR., ChangJ-L, CarrollJ., SonbolianN., LarsonC.E.Acute rhabdomyolysis following halothane anaesthesia without succinylcholine. Anesthesiology1987; 67: 856–857.
15.
ChalkiadisG.A., BranchK.G.Cardiac arrest after Isoflurane anaesthesia in a patient with Duchenne's muscular dystrophy. Anaesthesia1990; 45: 22–25.
16.
DubowitzV.The muscular dystrophies. Postgrad Med J1992; 68: 500–506.
17.
MillerG., WesselH.B.Diagnosis of Dystrophinopathies: review for the Clinician. Pediatr Neurol1993; 9: 3–9.
18.
BushbyK.M.D.Recent advances in understanding muscular dystrophy. Arch. of Disease in Childhood1992; 67: 1310–1312.
19.
MedoriR., BrookeM.H., WaterstonR.H.Genetic abnormalities in Duchenne and Becker dystrophies: clinical correlations. Neurology1989; 39: 461–465.
20.
BaumbachL.L., ChamberlainJ.S., WardP.A., FarwellN.J., CaskeyC.T.Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies. Neurology1989; 39: 465–474.
21.
BushbyK.M.D., ThambyayahM., Gardner-MedwinD.Prevalence and incidence of Becker muscular dystrophy. Lancet1991; 337: 1022–1024.
22.
BaudendistelL., GoudsouzianN., CoteC., StraffordM.End-tidal CO2 monitoring. Its use in the diagnosis and management of malignant hyperthermia. Anaesthesia1984; 39: 1000–1003.
23.
GronertG.A., FowlerW., CardinetG.H., GrixA., EllisW.G., SchartzM.Z.Absence of malignant hyperthermia contractures in Becker-Duchenne dystrophy at age 2. Muscle Nerve1992; 15: 52–56.
24.
OhlendickK., MatsumuraK., IonasescuV.V.Duchenne muscular dystrophy. Deficiency of dystrophin-associated proteins in the sarcolemma. Neurology1993; 43: 795–800.
25.
BrownwellA.K.W.Malignant hyperthermia: relationship to other diseases. Br J Anaesth1988; 60: 303–308.
26.
PrendergastB.D., GeorgeC.F.Drug-induced rhabdomyolysis—mechanisms and management. Postgrad Med J1993; 69: 333–336.
27.
OkaS., IgarashiY., TakagiA., NishidaM., SatoK., NakadaK., IkedaK.Malignant hyperpyrexia and Duchenne muscular dystrophy. A case report. Can Anaesth Soc J1982; 29: 627–629.
BrownwellA.K.W., FowlowS.B., PaasukeR.T.Coexistence of malignant hyperthermia and Duchenne muscular dystrophy in the same pedigree. Neurology1985; 35 (Suppl 1): 195.
30.
ToninP., LewisP., ServideiS., DiMauroS.Metabolic causes of myoglobinurea. Ann Neurol1990; 27: 181–185.
31.
Lehmann-HornF., IaizzoP.A.Are myotonias and periodic paralyses associated with susceptibility to malignant hyperthermia?Br J Anaesth1990; 65: 692–697.
32.
Ibraghimov-BeskrovnayaO., ErvastiJ.M., LeveilleC.I., SlaughterC.A., SernettS.W., CampbellK.P.Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature1992; 355: 696–702.
FrancoA.Jr, LansmanJ.B.Calcium entry through stretch inactivated ion channels in mdx myotubules. Nature1990; 344: 670–673.
35.
MenkeA., JockuschH.Decreased osmotic stability of dystrophin-less muscle cells from the MDX mouse. Nature1991; 349-69–71.
36.
RyanJ.F., KagenL.J., HymanA.I.Myoglobinuria after a single dose of succinylcholine. N Engl J Med1971; 285: 824–827.
37.
TammistoT., AiraksinenM.Increase of creatine kinase activity in serum as a sign of muscular injury caused by intermittently administered suxamethonium during halothane anaesthesia. Br J Anaesth1966; 38: 510–515.
38.
FletcherJ.E., RosenbergH.In vitro interaction between halothane and succinylcholine in human skeletal muscle: Implications for malignant hyperthermia and masseter muscle rigidity. Anesthesiology1985; 63: 190–194.
39.
HarringtonJ.F., FordD.J., StrikerT.W.Myoglobinuria after succinylcholine in children undergoing halothane and non-halothane anaesthesia. Anesthesiology1984; 61: A431.
40.
WorthanH.M., KubanK.C.K., SullivanK.F., BrensanM.J.A national survey of anaesthetic complications in children with Duchenne's muscular dystrophy. Anesth Analg1987; 66: S190.
41.
WangJ.M., StanleyT.H.Duchenne muscular dystrophy and malignant hyperthermia—two case reports. Can Anaesth Soc J1986; 33: 492–497.
AzarI.The response of patients with neuromuscular disorders to muscle relaxants: A review. Anesthesiology1984; 61: 173–187.
44.
SethnaN.F., RockoffM.A., WorthenH.M., RosnowJ.M.Anaesthesia related complications in children with Duchenne muscular dystrophy. Anesthesiology1988; 68: 462–465.
45.
RichardsW.C.Anaesthesia and serum creatine phosphokinase levels in patients with Duchenne's pseduohypertrophic muscular dystrophy. Anesth Intens Care1972; 1: 150–153.
46.
HoffmanE.P., FischbeckK.H., BrownR.H.Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy. N Engl J Med1988; 318: 1363–1368.
47.
LittlefordJ.A., PatelL.R., BoseD., CameronC.B., McKillopC.Masseter muscle spasm in children: Implications of continuing the triggering anaesthetic. Anesth Analg1991; 72: 151–160.