(Q52048583)

English

Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.

scientific article published in September 1991

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scholarly article

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity. (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

1 reference

based on heuristic

inferred from title

triosephosphate isomerase deficiency

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based on heuristic

inferred from title

4

object named as

M Gahr

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

author name string

S W Eber

1

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

A Pekrun

2

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

A Bardosi

3

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

W K Krietsch

5

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

J Krüger

6

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

R Matthei

7

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

W Schröter

8

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

publication date

1 September 1991

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

European Journal of Pediatrics

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

150

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

11

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Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

761-766

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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inferred from PubMed ID database lookup

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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Stepwise degradations and deamidation of the eye lens protein α-crystallin in ageing

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

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Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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Polymorphonuclear leukocyte function in term and preterm newborn infants

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https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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Posttranslational modifications of enzymes

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https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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inferred from PubMed ID database lookup

Hereditary deficiency of phosphoglycerate kinase: a new variant in erythrocytes and leucocytes, not associated with haemolytic anaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary deficiency of triosephosphate isomerase in four unrelated families

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of human triosephosphate isomerase isozymes: further evidence for the single structural locus hypothesis with Japanese variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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Triosephosphate isomerase deficiency. A case report with neuropathological findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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Congenital hemolytic anemia due to triosephosphate isomerase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Isolation and Crystallization of Yeast and Rabbit Liver Triose Phosphate Isomerase and a Comparative Characterization with the Rabbit Muscle Enzyme

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triose phosphate isomerase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

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Electrophoretic abnormality in triosephosphate isomerase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

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/1959537

12 December 2020

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Phagocytic activities in neonatal monocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary triose phosphate isomerase deficiency: seven new homozygous cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triose phosphate isomerase deficiency: report of a family.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human triose-phosphate isomerase deficiency: a single amino acid substitution results in a thermolabile enzyme

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucuronyl transferase deficiency and mild hereditary spherocytosis: effect of splenectomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

based on heuristic

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Triosephosphate isomerase deficiency: 2 new cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/1959537

12 December 2020

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Identifiers

10.1007/BF02026706

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/1959537

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