(Q67355186)

English

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

scientific article published on 01 June 1978

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669702%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

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

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669702%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

triosephosphate isomerase deficiency

1 reference

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inferred from title

neuromuscular disease

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hemolytic anemia

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author name string

J L Vives-Corrons

1

1 reference

Europe PubMed Central

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12 September 2019

H Rubinson-Skala

2

1 reference

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12 September 2019

M Mateo

3

1 reference

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12 September 2019

J Estella

4

1 reference

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12 September 2019

E Feliu

5

1 reference

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12 September 2019

J C Dreyfus

6

1 reference

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12 September 2019

publication date

1 June 1978

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12 September 2019

1 reference

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12 September 2019

42

1 reference

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12 September 2019

171-180

1 reference

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12 September 2019

2

1 reference

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12 September 2019

https://scigraph.springernature.com/pub.10.1007/bf00283637

0 references

HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

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inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

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A new isozyme of triose phosphate isomerase specific to hominoids.

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

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A newly defined X-linked trait in man with demonstration of the Lyon effect in carrier females

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

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Acquired granulocyte disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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Deficiencies associated with Embden-Meyerhof pathway and other metabolic pathways

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

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Biological defense mechanisms. The effect of bacteria and serum on superoxide production by granulocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: Clinical and familial studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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Comparison of the electrophoretic properties of triosephosphate isomerases of various tissues and species.

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

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[Acquired erythroenzymopathies. I. Quantitative anomalies observed in 100 cases of various hemopathies]

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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Congenital hemolytic anemia due to triosephosphate isomerase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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Probable Localization of a Triosephosphate Isomerase Gene to the Short Arm of the Number 5 Human Chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on erythrocyte glycolysis. I. Determination of the glycolytic intermediates in human erythrocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triose phosphate isomerase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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Electrophoretic abnormality in triosephosphate isomerase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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A unique electrophoretic pattern of triosephosphate isomerase in human cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

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The hemolytic effect of primaquine. VI. An in vitro test for sensitivity of erythrocytes to primaquine

1 reference

https://pubmed.ncbi.nlm.nih.gov/669702

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00283637

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:669702%20AND%20SRC:MED&resulttype=core&format=json

12 September 2019

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

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12 September 2019

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