(Q28341674)

English

Deficit of uridine diphosphate galactose in galactosaemia

scientific article (publication date: 1989)

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scholarly article

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Deficit of uridine diphosphate galactose in galactosaemia (English)

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author name string

W G Ng

1

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Y K Xu

2

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F R Kaufman

3

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G N Donnell

4

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language of work or name

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publication date

1989

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Journal of Inherited Metabolic Disease

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12

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257-66

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3

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Hereditary orotic aciduria: long-term therapy with uridine and a trial of uracil

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https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Curious neurologic sequelae in galactosemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Observations on the influence of orotic acid on galactosemetabolism in congenital galactosemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new mass screening method for determining UDP-galactose in blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical studies of a human low‐activity galactose‐1‐phosphate uridyl transferase variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of galactose-1-phosphate in erythrocytes: A rapid and simple enzymatic method

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neuropathology of galactosemia. A histopathological and biochemical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyruvate carboxylase defect: metabolic studies on cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibition and inactivation of bovine mammary and liver UDP-galactose-4-epimerases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Speech and language deficits in early-treated children with galactosemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibitor studies on uridine diphosphoglucose pyrophosphorylase

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation of ovarian function with galactose-1-phosphate uridyl transferase levels in galactosemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formation of Galactose-1-Phosphate from Uridine Diphosphate Galactose in Erythrocytes from Patients with Galactosemia[31]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein measurement with the Folin phenol reagent

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive cerebellar and extrapyramidal motor disturbances in galactosaemic twins.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uridine diphosphate glucose pyrophosphorylase. IV. Crystallization and properties of the enzyme from human liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypergonadotropic hypogonadism in female patients with galactosemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2515367

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01799215

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Springer Nature article ID

10.1007/bf01799215

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