(Q33354440)

26 July 2017

1 reference

title

ON THE ROLE OF BLOOD CELLS IN THE DIAGNOSIS OF HEREDITARY METABOLIC DISEASES (English)

1 reference

reason for deprecated rank

26 July 2017

�ber die Rolle der Blutzellen in der Diagnostik erblicher Stoffwechselkrankheiten (German)

marking inconsistent with the registered/official identifier/name

1 reference

14 January 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

glucose-6-phosphate dehydrogenase deficiency

14 January 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

thrombocytopenic purpura

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

aspartate transaminase

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

glucosephosphates

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

Clinical Enzyme Test

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

1 reference

Glucose-6-phosphate dehydrogenase

14 January 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

author name string

F. LINNEWEH

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14092943

14 January 2024

language of work or name

German

0 references

publication date

1 October 1963

1 reference

full work available at URL

26 July 2017

http://link.springer.com/content/pdf/10.1007/BF01478534.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF01478534/fulltext.html

14 January 2024

1 reference

http://link.springer.com/content/pdf/10.1007/BF01478534

14 January 2024

1 reference

14 January 2024

published in

Klinische Wochenschrift

1 reference

26 July 2017

volume

41

1 reference

26 July 2017

page(s)

937-941

1 reference

Advances in the recognition of heterozygous characteristics in hereditary enzymopathies

26 July 2017

cites work

1 reference

12 December 2020

The enzymic defect of hereditary methemoglobinemia: diaphorase

1 reference

12 December 2020

The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia

1 reference

12 December 2020

A nanomole adaption of the automatic amino acid analysis according to Spackman, Stein, and Moore (1985)

1 reference

12 December 2020

Phosphorylase activity in leucocytes from patients with glycogen-storages disease

1 reference

12 December 2020

A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency: investigation of platelet enzymes

1 reference

12 December 2020

Leukocyte debranching enzyme in glycogen storage disease

1 reference

12 December 2020

Metabolism of the white blood cells in maple-syrup-urine disease

1 reference

12 December 2020

[Hemolysis and absence of glucose-6-phosphate dehydrogenase in erythrocytes; an enzyme abnormality of erythrocytes]

1 reference

12 December 2020

PYRIMIDINE METABOLISM IN MAN. IV. THE ENZYMATIC DEFECT OF OROTIC ACIDURIA.

1 reference

12 December 2020

A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency. II. Investigation of leukocyte enzymes

1 reference

12 December 2020

Enzymatic deficiency in primaquine-sensitive erythrocytes

1 reference

12 December 2020

Metabolic observations on the erythrocytes from cases of galactosaemia

1 reference

12 December 2020

Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia

1 reference

12 December 2020

Low leukocyte phosphorylase in hepatic phosphorylase-deficient glycogen storage disease

1 reference

12 December 2020

Detection of congenital galactosemia and the carrier state using galactose C14 and blood cells

1 reference

12 December 2020

Uridyl transferases and the formation of uridine diphosphogalactose

1 reference

12 December 2020

Studies on the pathogenesis of haemolysis in hereditary spherocytosis

1 reference

12 December 2020

Glucose-6-phosphatase of the liver in glycogen storage disease

1 reference

12 December 2020

Hereditary enzymatic effects as illustrated by hypophosphatasia

1 reference

12 December 2020

Enzymatic Deficiency in Primaquine-Sensitive Erythrocytes

series ordinal

1

1 reference

Uridyl Transferases and the Formation of Uridine Triphosphate : Uridyl Transferases and the Formation of Uridine Diphosphogalactose

14 January 2024

series ordinal

9

1 reference

14 January 2024

24

59

XXII

V. Schwarz

1955

1 reference

14 January 2024

Identifiers

DOI

10.1007/BF01478534

1 reference

release_hsld27xokjbkbkc5uca7sglujq

26 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hsld27xokjbkbkc5uca7sglujq

24 November 2022

mapped directly with Wikidata item

1 reference