Rhabdomyolysis: a review (Q33957693)

30 July 2017

1 reference

title

Rhabdomyolysis: a review (English)

1 reference

30 July 2017

1 reference

Jason D Warren

1

1 reference

PubMed ID

11870710

30 July 2017

Peter C Blumbergs

series ordinal

2

1 reference

PubMed ID

11870710

30 July 2017

Philip D Thompson

series ordinal

3

1 reference

30 July 2017

1 March 2002

1 reference

30 July 2017

1 reference

30 July 2017

25

1 reference

30 July 2017

3

1 reference

30 July 2017

332-347

1 reference

Acute rhabdomyolysis after concurrent administration of interleukin-2, interferon-alfa, and chemotherapy for metastatic melanoma

30 July 2017

1 reference

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

21 January 2018

1 reference

Gasoline vapors induce severe rhabdomyolysis.

21 January 2018

1 reference

Early management of shock and prophylaxis of acute renal failure in traumatic rhabdomyolysis

21 January 2018

1 reference

Acute renal failure after a meal of quail.

21 January 2018

1 reference

21 January 2018

1 reference

21 January 2018

MUSCLE G6PD DEFICIENCY

1 reference

Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria

21 January 2018

1 reference

Neuroleptic malignant syndrome.

21 January 2018

1 reference

Neuroleptic Malignant syndrome caused by dopamine-depleting drugs in a patient with Huntington disease

21 January 2018

1 reference

Crush Injuries with Impairment of Renal Function

21 January 2018

1 reference

The membrane-associated 40 KD fatty acid binding protein (Berk's protein), a putative fatty acid transporter is present in human skeletal muscle

21 January 2018

1 reference

Acute rhabdomyolysis in patients infected by human immunodeficiency virus.

21 January 2018

1 reference

Disorders of lipid metabolism in skeletal muscle

21 January 2018

1 reference

21 January 2018

1 reference

Rhabdomyolysis in hypokalaemic periodic paralysis: a clue to the mechanism that terminates the paralytic attack?

21 January 2018

1 reference

Lipid-lowering drugs and mitochondrial function: effects of HMG-CoA reductase inhibitors on serum ubiquinone and blood lactate/pyruvate ratio

21 January 2018

1 reference

Rhabdomyolysis and acute renal failure resulting from alcohol and drug abuse

21 January 2018

1 reference

Muscle Carnitine Palmityltransferase Deficiency and Myoglobinuria

21 January 2018

1 reference

Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study

21 January 2018

1 reference

Nifedipine Diminishes Exercise-Induced Muscle Damage in Mouse

21 January 2018

1 reference

Pathogenesis and treatment of neuroleptic malignant syndrome

21 January 2018

1 reference

Rhabdomyolysis after intramuscular iron-dextran in malabsorption

21 January 2018

1 reference

Hypothyroid myopathy: apropos of a case with a great increase of creatine phosphokinase, myoglobinemia and transient kidney failure

21 January 2018

1 reference

Rhabdomyolysis and hypoxia associated with prolonged propofol infusion in children

21 January 2018

1 reference

Acute peripheral neuropathy, rhabdomyolysis, and severe lactic acidosis associated with 3243 A to G mitochondrial DNA mutation

21 January 2018

1 reference

The anesthetic myopathies and malignant hyperthermias.

21 January 2018

1 reference

Blood lactate threshold and type II fibre predominance in patients with exertional heatstroke

21 January 2018

1 reference

Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient

21 January 2018

1 reference

Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families.

21 January 2018

1 reference

Altered brain development in Turner's syndrome: an event-related potential study.

21 January 2018

1 reference

Rhabdomyolysis secondary to keyboard overuse: occupational hazard of the computer age.

21 January 2018

1 reference

Clinical pharmacology, therapeutic use and potential of COMT inhibitors in Parkinson's disease

21 January 2018

1 reference

Medium chain 3-ketoacyl-coenzyme A thiolase deficiency: a new disorder of mitochondrial fatty acid beta-oxidation

21 January 2018

1 reference

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

21 January 2018

1 reference

A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria

21 January 2018

1 reference

Catastrophic medical events with exhaustive exercise: "white collar rhabdomyolysis".

21 January 2018

1 reference

Postpartum manifestation of a necrotising lipid storage myopathy associated with muscle carnitine deficiency

21 January 2018

1 reference

Clinical features, pathogenesis and management of drug-induced rhabdomyolysis

21 January 2018

1 reference

Exercise-induced muscle damage

21 January 2018

1 reference

Paraneoplastic necrotizing myopathy: clinical and pathological features

21 January 2018

1 reference

Nicotinic acid-associated myopathy: a report of three cases

21 January 2018

1 reference

The pathophysiology of altered calcium metabolism in rhabdomyolysis-induced acute renal failure. Interactions of parathyroid hormone, 25-hydroxycholecalciferol, and 1,25-dihydroxycholecalciferol

21 January 2018

1 reference

Malignant hyperthermia and central core disease: disorders of Ca2+ release channels

21 January 2018

1 reference

Status dystonicus: the syndrome and its management.

21 January 2018

1 reference

Biochemical evidence for a complex involving dihydropyridine receptor and ryanodine receptor in triad junctions of skeletal muscle

21 January 2018

1 reference

Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle

21 January 2018

1 reference

Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy

21 January 2018

1 reference

Very long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria.

21 January 2018

1 reference

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

21 January 2018

1 reference

Acute necrotizing myopathy and podophyllin toxicity. Report of a fatal case

21 January 2018

1 reference

Dantrolene sodium reduces the enhanced leakage of creatine kinase caused by ethanol, cocaine, and electrical stimulation in isolated fast and slow muscles of rat.

21 January 2018

1 reference

Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency

21 January 2018

1 reference

In vitro contraction test for malignant hyperthermia in patients with unexplained recurrent rhabdomyolysis

21 January 2018

1 reference

Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency.

21 January 2018

1 reference

Drug-induced rhabdomyolysis--mechanisms and management

21 January 2018

1 reference

Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

21 January 2018

1 reference

Rhabdomyolysis and drugs of abuse

21 January 2018

1 reference

Diabetic muscular infarction

21 January 2018

1 reference

Cramping pain and prolonged elevation of serum creatine kinase levels in a patient with Guillain-Barré syndrome following Campylobacter jejuni enteritis

21 January 2018

1 reference

Recognition and management of fatty acid oxidation defects: a series of 107 patients.

21 January 2018

1 reference

Idiopathic rhabdomyolysis.

21 January 2018

1 reference

High-dose itraconazole in the treatment of severe mycoses

21 January 2018

1 reference

Infectious etiologies of rhabdomyolysis: three case reports and review

21 January 2018

1 reference

Gene shifting: a novel therapy for mitochondrial myopathy.

21 January 2018

1 reference

Short-chainL-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: A new cause for recurrent myoglobinuria and encephalopathy

21 January 2018

1 reference

Metabolic causes of myoglobinuria

21 January 2018

1 reference

Carnitine palmitoyl transferase deficiency in malignant hyperthermia

21 January 2018

1 reference

Acute pediatric rhabdomyolysis.

21 January 2018

1 reference

Mitochondrial calcium overload: A general mechanism for cell-necrosis in muscle diseases

21 January 2018

1 reference

Myoadenylate deaminase deficiency: successful symptomatic therapy by high dose oral administration of ribose

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MUS.10053

1 reference

30 July 2017

1 reference

PubMed ID

11870710