Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency. (Q52059815)

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scientific article published in January 1990

Language	Label	Description	Also known as
English	Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.	scientific article published in January 1990

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

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

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

author name string

A Bardosi

1

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

S W Eber

2

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

M Hendrys

3

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

A Pekrun

4

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

publication date

1 January 1990

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

Acta Neuropathologica

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

79

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

4

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

387-394

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary deficiency of lactate dehydrogenase M-subunit

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

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/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

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/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triosephosphate isomerase deficiency. A case report with neuropathological findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Muscle Phosphoglycerate Mutase Deficiency: Newly Discovered Metabolic Myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructural and histochemical abnormalities of skeletal muscle in a patient with a new variant (type Homburg) of glucosephosphate isomerase (GPI) deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

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/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

alpha-Glycerophosphate oxidase of flight muscle mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generalised glucosephosphate isomerase (GPI) deficiency causing haemolytic anaemia, neuromuscular symptoms and impairment of granulocytic function: a new syndrome due to a new stable GPI variant with diminished specific activity (GPI Homburg).

1 reference

https://pubmed.ncbi.nlm.nih.gov/2339591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00308714

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

release_6c4s7z4fpva5zfg6rl5emnx2zq

1 reference

https://api.fatcat.wiki/v0/release/6c4s7z4fpva5zfg6rl5emnx2zq

24 November 2022

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mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 April 2018

http://europepmc.org/abstract/MED/2339591

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