(Q72476120)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7837763%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

Menstrual cycle and gonadal steroid effects on symptomatic hyperammonaemia of urea-cycle-based and idiopathic aetiologies (English)

1 reference

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27 October 2019

author name string

W W Grody

1

1 reference

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27 October 2019

R J Chang

2

1 reference

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27 October 2019

N M Panagiotis

3

1 reference

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27 October 2019

D Matz

4

1 reference

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27 October 2019

S D Cederbaum

5

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27 October 2019

publication date

1 January 1994

1 reference

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Journal of Inherited Metabolic Disease

27 October 2019

published in

1 reference

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27 October 2019

volume

17

1 reference

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27 October 2019

issue

5

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27 October 2019

page(s)

566-574

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https://scigraph.springernature.com/pub.10.1007/bf00711592

27 October 2019

exact match

0 references

cites work

Differentiation of transient hyperammonemia of the newborn and urea cycle enzyme defects by clinical presentation

1 reference

12 December 2020

ENZYMES OF ARGININE METABOLISM IN MAMMALIAN CELL CULTURE. I. REPRESSION OF ARGININOSUCCINATE SYNTHETASE AND ARGININOSUCCINASE

1 reference

12 December 2020

Electroencephalogram Changes Secondary to Asparaginase

1 reference

12 December 2020

Lysinuric protein intolerance

1 reference

12 December 2020

Treatment of hyperammonemic coma caused by inborn errors of urea synthesis

1 reference

12 December 2020

Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma

1 reference

12 December 2020

Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation

1 reference

12 December 2020

Advances in the detection of amino acids in biological fluids

1 reference

12 December 2020

Qualitative abnormality of liver argininosuccinate synthetase in a patient with citrullinemia

1 reference

12 December 2020

[Hyperammonemia coma following uretero-sigmoidostomy]

1 reference

12 December 2020

Regulation of glucocorticoids of arginase and argininosuccinate synthetase in cultured rat hepatoma cells

1 reference

12 December 2020

Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome

1 reference

12 December 2020

Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia

1 reference

12 December 2020

Hyperammonemia in pediatric diseases

1 reference

12 December 2020

Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysis

1 reference

12 December 2020

Treatment of adult-type citrullinemia with administration of citrate

1 reference

12 December 2020

Studies on the pathophysiology of encephalopathy in Reye's syndrome; Hyperammonemia in Reye's syndrome

1 reference

12 December 2020

Transient idiopathic hyperammonaemia in adults

1 reference

12 December 2020

Ammonia encephalopathy secondary to urinary tract infection with Proteus mirabilis

1 reference

12 December 2020

Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoids

1 reference

12 December 2020

Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in women

1 reference

12 December 2020

Hepatic encephalopathy

1 reference

12 December 2020

Properties of fetal and adult red blood cell arginase: a possible prenatal diagnostic test for arginase deficiency

1 reference

12 December 2020

Hyperargininemia with Arginase Deficiency

1 reference

12 December 2020

Current status of hyperammonemic syndromes

1 reference

12 December 2020

Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme

1 reference

12 December 2020

Arginine therapy of argininosuccinase deficiency

1 reference

12 December 2020

Valproate-induced inhibition of urea synthesis and hyperammonaemia in healthy subjects

1 reference

12 December 2020

Ornitbine transcarbamylase deficiency in the newborn infant

1 reference

12 December 2020

Lysinuric protein intolerance: a two-year trial of dietary supplementation therapy with citrulline and lysine

1 reference

12 December 2020

Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00711592

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7837763%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference