Literature DB >> 14151259

[HEREDITARY GLUCOSE-6-PHOSPHATE DEHYDROGENASE INACTIVITY. METABOLIC DISORDER HEMOLYTIC MECHANISM AND GENETICS].

G FLATZ.   

Abstract

Keywords:  GENETICS, HUMAN; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY; HEMOLYSIS; METABOLIC DISEASES; PHYSIOLOGY; REVIEW

Mesh:

Substances:

Year:  1964        PMID: 14151259

Source DB:  PubMed          Journal:  Med Klin        ISSN: 0025-8458


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  4 in total

1.  [CHRONIC, NON-SPHEROCYTIC HEMOLYTIC JAUNDICE IN TOTAL ABSENCE OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY OF THE ERYTHROCYTES].

Authors:  H H HENNEMANN; U ESSERS; G STECHER
Journal:  Klin Wochenschr       Date:  1964-12-15

Review 2.  [Hereditary nonspherocytic hemolytic anemias].

Authors:  D Busch
Journal:  Blut       Date:  1966-05

3.  [Use of sulfamethoxypyrazine in persons with an erythrocytic glucose-6-phosphate deficiency].

Authors:  G Flatz; B Voss; S Voss
Journal:  Klin Wochenschr       Date:  1970-01-15

4.  [Glucose-6-phosphate dehydrogenase deficiency of erythrocytes in 3 German children. Determination of a new mutation].

Authors:  V Weidtman; O Tönz
Journal:  Klin Wochenschr       Date:  1966-04-15
  4 in total

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