(Q93648045)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4065896%20AND%20SRC:MED&resulttype=core&format=json

8 May 2020

title

Hereditary triose phosphate isomerase deficiency: seven new homozygous cases (English)

1 reference

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8 May 2020

1 reference

R Rosa

1

1 reference

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8 May 2020

M O Prehu

2

1 reference

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8 May 2020

M C Calvin

3

1 reference

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8 May 2020

J Badoual

4

1 reference

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8 May 2020

D Alix

5

1 reference

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8 May 2020

R Girod

6

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8 May 2020

publication date

1 January 1985

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8 May 2020

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8 May 2020

volume

71

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8 May 2020

page(s)

235-240

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8 May 2020

issue

3

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HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

8 May 2020

cites work

1 reference

12 December 2020

The isolation and characterization of the multiple forms of human skeletal muscle triosephosphate isomerase

1 reference

12 December 2020

Familial diphosphoglyceratemutase deficiency. Influence on the oxygen affinity curves of hemoglobin

1 reference

12 December 2020

Origin of the triosephosphate isomerase isozymes in humans: genetic evidence for the expression of a single structural locus

1 reference

12 December 2020

Neurological findings in triosephosphate isomerase deficiency

1 reference

12 December 2020

Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany--a study of 3000 people

1 reference

12 December 2020

Molecular basis for the accumulation of acidic isozymes of triosephosphate isomerase on aging

1 reference

12 December 2020

Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants

1 reference

12 December 2020

Hereditary deficiency of triosephosphate isomerase in four unrelated families

1 reference

12 December 2020

Triosephosphate isomerase deficiency. A case report with neuropathological findings.

1 reference

12 December 2020

Congenital hemolytic anemia due to triosephosphate isomerase deficiency

1 reference

12 December 2020

Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain

1 reference

12 December 2020

[Diphosphoglyceromutase deficiency: new cases associated with erythrocytosis]

1 reference

12 December 2020

Electrophoretic abnormality in triosephosphate isomerase deficiency

1 reference

12 December 2020

Genetic and non-genetic variation of triose phosphate isomerase isozymes in human tissues

1 reference

12 December 2020

12pter to 12p12.2: possible assignment of human triose phosphate isomerase

1 reference

12 December 2020

Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p

1 reference

12 December 2020

Rate of spontaneous mutation at human loci encoding protein structure

1 reference

12 December 2020

International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysis.

1 reference

12 December 2020

Frequency of enzyme deficiency variants in erythrocytes of newborn infants

1 reference

12 December 2020

Electrophoretic variants of blood proteins in Japanese. III. Triosephosphate isomerase

1 reference

12 December 2020

The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes

1 reference

12 December 2020

Enzymatic mechanisms of red cell adaptation to anemia.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00284582

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4065896%20AND%20SRC:MED&resulttype=core&format=json

8 May 2020

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