(Q31893794)

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Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies

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scholarly article

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Europe PubMed Central

PubMed publication ID

4 July 2017

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Europe PubMed Central

Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

glutathione synthetase deficiency

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based on heuristic

inferred from title

author name string

Corrons JL

1

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Alvarez R

2

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Pujades A

3

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Zarza R

4

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Oliva E

5

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Lasheras G

6

1 reference

Europe PubMed Central

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4 July 2017

Callis M

7

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Ribes A

8

1 reference

Europe PubMed Central

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4 July 2017

Gelbart T

9

1 reference

Europe PubMed Central

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4 July 2017

Beutler E

10

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4 July 2017

language of work or name

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publication date

1 February 2001

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4 July 2017

British Journal of Haematology

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4 July 2017

112

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Europe PubMed Central

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4 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

475-482

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Erythrocyte glutathione synthetase deficiency leads not only to glutathione but also to glutathione-S-transferase deficiency

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

γ-Glutamyl-cysteine synthetase deficiency. A cause of hereditary hemolytic anemia

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Glutathione Synthetase Deficiency as a Cause of Hereditary Hemolytic Disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Chronic intrastriatal L-pyroglutamate: neuropathology and neuron sparing like Huntington's disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

5-Oxoprolinuria in an adolescent with chronic metabolic acidosis, mental retardation, and psychosis.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Chronic inhibition of glutamate uptake produces a model of slow neurotoxicity

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Mutations in the glutathione synthetase gene cause 5-oxoprolinuria

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Oxidative damage to neutrophils in glutathione synthetase deficiency

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2001.02526.X

21 January 2018

Identifiers

10.1046/J.1365-2141.2001.02526.X

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

ResearchGate publication ID

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