Hyperammonemic encephalopathy caused by carnitine deficiency (Q36607259)

15 August 2017

Hyperammonemic encephalopathy caused by carnitine deficiency (English)

1 reference

15 August 2017

Berkeley N Limketkai

1

1 reference

PMC publication ID

2359173

15 August 2017

Stephen D Zucker

series ordinal

2

1 reference

15 August 2017

13 December 2007

1 reference

Journal of General Internal Medicine

15 August 2017

1 reference

15 August 2017

23

1 reference

15 August 2017

2

1 reference

15 August 2017

210-213

1 reference

The nutritional relationship linking sulfur to nitrogen in living organisms

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Effects of L-carnitine in patients with hepatic encephalopathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Kinetics, pharmacokinetics, and regulation of L-carnitine and acetyl-L-carnitine metabolism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Sulfur amino acid metabolism: pathways for production and removal of homocysteine and cysteine

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Carnitine transport: pathophysiology and metabolism of known molecular defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Regulation of mitochondrial carbamoyl-phosphate synthetase 1 activity by active site fatty acylation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Valproate-induced hyperammonemic encephalopathy in the presence of topiramate

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Genetic epidemiology of the carnitine transporter OCTN2 gene in a Japanese population and phenotypic characterization in Japanese pedigrees with primary systemic carnitine deficiency

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Carnitine deficiency and hyperammonemia in children receiving valproic acid with and without other anticonvulsant drugs

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Molecular and functional identification of sodium ion-dependent, high affinity human carnitine transporter OCTN2

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

The carnitine acyltransferases and their role in modulating acyl-CoA pools

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Reye's syndrome in the adult: case report and review of the literature.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Portal-Systemic Encephalopathy and Portacaval Anastomosis: A Prospective, Controlled Investigation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Carnitine prevents Reye-like syndrome in atypical carnitine deficiency.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Serum carnitine during valproic acid therapy

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Effects of a single, short intravenous dose of acetyl-L-carnitine on pattern-reversal visual-evoked potentials in cirrhotic patients with hepatic encephalopathy

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Hyperammonemic encephalopathy induced by a combination of valproate and pivmecillinam

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Carnitine transporter defect diagnosed by newborn screening with electrospray tandem mass spectrometry

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Systemic carnitine deficiency simulating recurrent Reye syndrome.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride diet.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2359173

Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle

20 September 2018

1 reference

12 December 2020

Correlation of carnitine levels to methionine and lysine intake

1 reference

12 December 2020

Ammonia encephalopathy secondary to urinary tract infection with Proteus mirabilis

1 reference

12 December 2020

Hyperammonemia during total parenteral nutrition in children

1 reference

12 December 2020

Carnitine deficiency and hyperammonemia associated with valproic acid therapy

1 reference

12 December 2020

Systemic carnitine deficiency: Clinical, biochemical, and morphological cure with L-carnitine

1 reference

12 December 2020

Effects of L-carnitine on urea synthesis following acute ammonia intoxication in mice

1 reference

12 December 2020

Renal handling of carnitine in children with carnitine deficiency and hyperammonemia associated with valproate therapy

1 reference

12 December 2020

Carnitine status in Reye and Reye-like syndromes

1 reference

12 December 2020

Fifteen years' experience with 212 hyperammonaemic cases at a Metabolic Unit

1 reference

12 December 2020

Prognostic factors of hepatic encephalopathy after portacaval anastomosis: a multivariate analysis in 50 patients

1 reference

12 December 2020

Deficient Muscle Carnitine Transport in Primary Carnitine Deficiency

1 reference

12 December 2020

10.1007/S11606-007-0473-0

Identifiers

DOI

1 reference

15 August 2017

1 reference

PMC publication ID

2359173

15 August 2017

PubMed publication ID

18080167

1 reference

PMC publication ID

2359173