Literature DB >> 13293306

Electrophoretic properties of myoglobin and its character in sickle-cell diseases and paroxysmal myoglobinuria.

T A PRANKERD.   

Abstract

Entities:  

Keywords:  ANEMIA, SICKLE CELL/blood in; HEMOGLOBIN; HEMOGLOBINURIA, PAROXYSMAL

Mesh:

Substances:

Year:  1956        PMID: 13293306     DOI: 10.1111/j.1365-2141.1956.tb06687.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


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  3 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.  The detection of myoglobin in urine and its distinction from normal and variant haemoglobins.

Authors:  F E Boulton; R G Huntsman
Journal:  J Clin Pathol       Date:  1971-12       Impact factor: 3.411

  3 in total

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