Literature DB >> 13634937

[Double albumin peak as a hereditary blood protein anomaly].

F WUHRMANN.   

Abstract

Entities:  

Keywords:  SERUM ALBUMIN

Mesh：

Substances：

Year:  1959        PMID： 13634937

Source DB:  PubMed          Journal:  Schweiz Med Wochenschr        ISSN： 0036-7672


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  5 in total

1.  [PROGRESSIVE SPINAL MUSCULAR ATROPHY IN PARALBUMINEMIA].

Authors:  M ZANGENEH; H G MERTENS; I SCHWARZE
Journal:  Dtsch Z Nervenheilkd       Date:  1964-08-14

2.  Observations on double albumin. II. A peptide difference between two genetically determined human serum albumins.

Authors:  D GITLIN; K SCHMID; D P EARLE; H GIVERLBER
Journal:  J Clin Invest       Date:  1961-05       Impact factor: 14.808

3.  Another example of slow albumin allotype.

Authors:  J P Martin; L C Legueult; C Ropartz; J Mauze; A Lescaroux; A Richard; D Chauvat
Journal:  Humangenetik       Date:  1971

4.  [A human serum albumin variant (bisalbuminaemia). Occurrence and heredity in a family (area of Berlin)].

Authors:  M Rose; J Blaszczyk; G Geserick
Journal:  Humangenetik       Date:  1971

5.  [Alloalbuminemia (double albuminemia)].

Authors:  A Fateh-Moghadam; J Eisenburg; R Lamerz
Journal:  Klin Wochenschr       Date:  1969-09-15
  5 in total

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