(Q33957693)

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Rhabdomyolysis: a review

scientific article

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scholarly article

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Europe PubMed Central

30 July 2017

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Europe PubMed Central

Rhabdomyolysis: a review (English)

1 reference

Europe PubMed Central

30 July 2017

1 reference

based on heuristic

inferred from title

author name string

Jason D Warren

1

1 reference

Europe PubMed Central

30 July 2017

Peter C Blumbergs

2

1 reference

Europe PubMed Central

30 July 2017

Philip D Thompson

3

1 reference

Europe PubMed Central

30 July 2017

publication date

1 March 2002

1 reference

Europe PubMed Central

30 July 2017

Muscle and Nerve

1 reference

Europe PubMed Central

30 July 2017

25

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Europe PubMed Central

30 July 2017

3

1 reference

Europe PubMed Central

30 July 2017

332-347

1 reference

Europe PubMed Central

30 July 2017

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Gasoline vapors induce severe rhabdomyolysis.

1 reference

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21 January 2018

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

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21 January 2018

Acute renal failure after a meal of quail.

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21 January 2018

Serotonin syndrome.

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21 January 2018

MUSCLE G6PD DEFICIENCY

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Neuroleptic malignant syndrome.

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Crush Injuries with Impairment of Renal Function

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Acute rhabdomyolysis in patients infected by human immunodeficiency virus.

1 reference

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21 January 2018

Disorders of lipid metabolism in skeletal muscle

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21 January 2018

1 reference

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21 January 2018

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

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21 January 2018

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

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21 January 2018

Rhabdomyolysis and acute renal failure resulting from alcohol and drug abuse

1 reference

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21 January 2018

Muscle Carnitine Palmityltransferase Deficiency and Myoglobinuria

1 reference

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21 January 2018

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

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21 January 2018

Nifedipine Diminishes Exercise-Induced Muscle Damage in Mouse

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21 January 2018

Pathogenesis and treatment of neuroleptic malignant syndrome

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21 January 2018

Rhabdomyolysis after intramuscular iron-dextran in malabsorption

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21 January 2018

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

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21 January 2018

Rhabdomyolysis and hypoxia associated with prolonged propofol infusion in children

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21 January 2018

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

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21 January 2018

The anesthetic myopathies and malignant hyperthermias.

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21 January 2018

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

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21 January 2018

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

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21 January 2018

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.

1 reference

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21 January 2018

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

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21 January 2018

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

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21 January 2018

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

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Clinical features, pathogenesis and management of drug-induced rhabdomyolysis

1 reference

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21 January 2018

Exercise-induced muscle damage

1 reference

https://api.crossref.org/works/10.1002%2FMUS.10053

21 January 2018

Paraneoplastic necrotizing myopathy: clinical and pathological features

1 reference

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21 January 2018

Nicotinic acid-associated myopathy: a report of three cases

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Status dystonicus: the syndrome and its management.

1 reference

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

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21 January 2018

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

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21 January 2018

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

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21 January 2018

Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiency

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Exertional rhabdomyolysis in a patient with calcium adenosine triphosphatase deficiency.

1 reference

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21 January 2018

Drug-induced rhabdomyolysis--mechanisms and management

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Rhabdomyolysis and drugs of abuse

1 reference

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21 January 2018

Diabetic muscular infarction

1 reference

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21 January 2018

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

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21 January 2018

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

1 reference

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21 January 2018

Idiopathic rhabdomyolysis.

1 reference

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21 January 2018

High-dose itraconazole in the treatment of severe mycoses

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21 January 2018

Infectious etiologies of rhabdomyolysis: three case reports and review

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21 January 2018

Gene shifting: a novel therapy for mitochondrial myopathy.

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Metabolic causes of myoglobinuria

1 reference

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21 January 2018

Carnitine palmitoyl transferase deficiency in malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1002%2FMUS.10053

21 January 2018

Acute pediatric rhabdomyolysis.

1 reference

https://api.crossref.org/works/10.1002%2FMUS.10053

21 January 2018

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

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Identifiers

10.1002/MUS.10053

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

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