Literature DB >> 14035019

Idiopathic recurrent rhabdomyolysis with myoglobinuria. Case report, with diagnostic recommendations and demonstration of unusual heme compounds in the urine.

R J KOSSMANN, W A CAMP, R L ENGLE.   

Abstract

Entities:  

Keywords:  MUSCULAR DISEASES; MYOGLOBIN

Mesh:

Substances:

Year:  1963        PMID: 14035019     DOI: 10.1016/0002-9343(63)90079-2

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


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  4 in total

1.  IDIOPATHIC RHABDOMYOLYSIS.

Authors:  E E WALLER
Journal:  Calif Med       Date:  1964-10

2.  HEREDITARY METABOLIC MYOPATHY WITH PAROXYSMAL MYOGLOBINURIA DUE TO ABNORMAL GLYCOLYSIS.

Authors:  L E LARSSON; H LINDERHOLM; R MUELLER; T RINGQVIST; R SOERNAES
Journal:  J Neurol Neurosurg Psychiatry       Date:  1964-10       Impact factor: 10.154

Review 3.  Idiopathic rhabdomyolysis.

Authors:  D C Savage; M Forbes; G W Pearce
Journal:  Arch Dis Child       Date:  1971-10       Impact factor: 3.791

4.  Myoglobinuria and skeletal muscle phosphorylase deficiency: report of a case of McArdle's disease.

Authors:  J C Nixon; W K Hobbs; J Greenblatt
Journal:  Can Med Assoc J       Date:  1966-05-07       Impact factor: 8.262

  4 in total

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