(Q44590938)

English

Urine uric acid to creatinine rtio--a screening test for inherited disorders of purine metabolism. Phosphoribosyltransferase (PRT) deficiency in X-linked cerebral palsy and in a variant of gout

scientific article published in October 1968

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Europe PubMed Central

PubMed publication ID

4 December 2017

Urine uric acid to creatinine rtio--a screening test for inherited disorders of purine metabolism. Phosphoribosyltransferase (PRT) deficiency in X-linked cerebral palsy and in a variant of gout (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

1 reference

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author name string

Kaufman JM

1

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Greene ML

2

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Europe PubMed Central

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4 December 2017

Seegmiller JE

3

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Europe PubMed Central

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4 December 2017

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publication date

1 October 1968

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Europe PubMed Central

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4 December 2017

The Journal of Pediatrics

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Europe PubMed Central

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4 December 2017

73

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Europe PubMed Central

PubMed publication ID

4 December 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

583-592

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980274-4

7 January 2021

Juvenile gout with brain involvement

1 reference

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7 January 2021

HEREDITARY CHOREOATHETOSIS, SELF-MUTILATION AND HYPERURICEMIA IN YOUNG MALES

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980274-4

7 January 2021

Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

1 reference

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7 January 2021

A specific enzyme defect in gout associated with overproduction of uric acid

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980274-4

7 January 2021

Treatment of x-linked primary hyperuricemia with allopurinol

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980274-4

7 January 2021

Biochemistry of uric acid and its relation to gout

1 reference

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7 January 2021

Biochemistry of uric acid and its relation to gout

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980274-4

7 January 2021

Biochemistry of uric acid and its relation to gout

1 reference

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7 January 2021

Relationships between glycogen storage disease and tophaceous gout

1 reference

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7 January 2021

Uric acid production in gout

1 reference

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7 January 2021

The nitrogen partition in newborn infant's urine

1 reference

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7 January 2021

Aminoimidazolecarboxamide excretion in vitamin-B12 and folic-acid deficiencies

1 reference

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7 January 2021

Urinary AICA (4-Amino-5-imidazolecarboxamide) Following an Oral Dose of AICA in Formiminotransferase Deficiency Syndrome

1 reference

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7 January 2021

Urinary Metabolites in Congenital Hyperuricosuria

1 reference

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7 January 2021

Hyperuricemia in mongolism

1 reference

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7 January 2021

Human circadian rhythms

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980274-4

7 January 2021

The renal excretion of uric acid in patients with gout and in nongouty subjects

1 reference

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7 January 2021

The Lesch-Nyhan Syndrome: Self-Destructive Biting, Mental Retardation, Neurological Disorder and Hyperuricaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980274-4

7 January 2021

based on heuristic

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Identifiers

10.1016/S0022-3476(68)80274-4

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

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