Literature DB >> 13312696

Idiopathic paroxysmal myoglobinuria; report of two cases and evaluation of the syndrome.

L REINER, N KONIKOFF, M D ALTSCHULE, G J DAMMIN, J P MERRILL.   

Abstract

Entities:  

Keywords:  HEMOGLOBINURIA, PAROXYSMAL

Mesh：

Year:  1956        PMID： 13312696     DOI： 10.1001/archinte.1956.00250230031004

Source DB:  PubMed          Journal:  AMA Arch Intern Med        ISSN： 0888-2479


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  5 in total

1.  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

2.  [Demonstration of myoglobin by means of starch block electrophoresis].

Authors:  H R MARTI
Journal:  Klin Wochenschr       Date:  1961-03-15

3.  ANNOTATIONS.

Authors: 
Journal:  Br Med J       Date:  1957-01-19

4.  Ultrastructural changes in muscle mitochondria in situ, including the apparent development of internal septa, associated with the uptake and release of calcium.

Authors:  S J Publicover; C J Duncan; J L Smith
Journal:  Cell Tissue Res       Date:  1977-12-19       Impact factor: 5.249

Review 5.  Idiopathic rhabdomyolysis.

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

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