(Q54290252)

27 May 2018

title

[Glucose-6-phosphate dehydrogenase defect in Germany. II. Properties of the enzyme (type "Freiburg")]. (English)

1 reference

27 May 2018

author name string

D Busch

series ordinal

1

1 reference

27 May 2018

K Boie

series ordinal

2

1 reference

27 May 2018

language of work or name

German

0 references

publication date

1 January 1970

1 reference

27 May 2018

published in

Klinische Wochenschrift

1 reference

27 May 2018

volume

48

1 reference

27 May 2018

issue

2

1 reference

27 May 2018

page(s)

74-78

1 reference

27 May 2018

The glutathione instability of drug-sensitive red cells; a new method for the in vitro detection of drug sensitivity

cites work

1 reference

12 December 2020

Improved method for the determination of blood glutathione

1 reference

12 December 2020

Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease

1 reference

12 December 2020

Evidence for four types of erythrocyte glucose-6-phosphate dehydrogenase from G-6-PD-deficient human subjects

1 reference

12 December 2020

Congenital nonspherocytic hemolytic anemia with deficiency of erythrocytic pyruvate kinase

1 reference

12 December 2020

ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN CAUCASIANS: NEW INHERITED VARIANT

1 reference

12 December 2020

Athens variant of glucose-6-phosphate dehydrogenase

1 reference

12 December 2020

Sex-linkage of the Glucose-6-phosphate Dehydrogenase Gene in Equidae

1 reference

12 December 2020

Erythrocyte isolation from blood with cotton

1 reference

12 December 2020

DIFFERENT ENZYMIC EXPRESSIONS OF MUTANTS OF HUMAN GLUCOSE-6-PHOSPHATE DEHYDROGENASE

1 reference

12 December 2020

Electrophoretic heterogeneity of glucose-6-phosphate dehydrogenase and its relationship to enzyme deficiency in man.

1 reference

12 December 2020

"CHICAGO I" VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN CONGENITAL HEMOLYTIC DISEASE

1 reference

12 December 2020

VARIATION OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN DIFFERENT POPULATIONS.

1 reference

12 December 2020

[Transformation of drug-sensitive erythropathy into chronic hemolytic anemia in glucose-6-phosphatedehydrogenase deficiency]

1 reference

12 December 2020

TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE

1 reference

12 December 2020

ELECTROPHORETICALLY SLOW VARIANTS OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE FROM RED CELLS OF NEGROES

1 reference

12 December 2020

[NAD-NADH, NADP-NADPH and GSSG-GSH in human erythrocytes].

1 reference

12 December 2020

[Hereditary non-spherocytic hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency. Formation of an enzyme protein with modified characteristics in the blood cells of a German family]

1 reference

12 December 2020

On 2 new cases of hereditary nonspherocytic hemolytic anemia associated with glucose-6-phosphate-dehydrogenase deficiency in a North-German family. I

1 reference

12 December 2020

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

12 December 2020

The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01484620

1 reference

27 May 2018

1 reference

27 May 2018