(Q48396811)

11 February 2018

title

The aetiology of neurological complications of organic acidaemias--a role for the blood-brain barrier. (English)

1 reference

11 February 2018

1 reference

S Kölker

1

1 reference

11 February 2018

S W Sauer

series ordinal

2

1 reference

11 February 2018

R A H Surtees

series ordinal

3

1 reference

11 February 2018

J V Leonard

series ordinal

4

1 reference

11 February 2018

publication date

14 October 2006

1 reference

11 February 2018

Journal of Inherited Metabolic Disease

published in

1 reference

11 February 2018

volume

29

1 reference

11 February 2018

issue

6

1 reference

11 February 2018

page(s)

701-4; discussion 705-6

1 reference

11 February 2018

https://scigraph.springernature.com/pub.10.1007/s10545-006-0415-8

exact match

0 references

cites work

Glutaric aciduria type I and kynurenine pathway metabolites: a modified hypothesis

1 reference

12 December 2020

Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohort

1 reference

12 December 2020

Bioenergetics in glutaryl-coenzyme A dehydrogenase deficiency: a role for glutaryl-coenzyme A.

1 reference

12 December 2020

Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency

1 reference

12 December 2020

L-2-hydroxyglutaric acidemia: A novel inherited neurometabolic disease

1 reference

12 December 2020

NMDA receptor activation and respiratory chain complex V inhibition contribute to neurodegeneration in d-2-hydroxyglutaric aciduria

1 reference

12 December 2020

Neurological outcome of methylmalonic acidaemia

1 reference

12 December 2020

Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiency.

1 reference

12 December 2020

Kynurenines in the CNS: from endogenous obscurity to therapeutic importance

1 reference

12 December 2020

Physiology and pathophysiology of organic acids in cerebrospinal fluid

1 reference

12 December 2020

Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Stroke-like encephalopathy in an infant with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.

1 reference

12 December 2020

Neurological manifestations of organic acid disorders.

1 reference

12 December 2020

Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Liver transplantation in urea cycle disorders

1 reference

12 December 2020

Transporter-mediated permeation of drugs across the blood-brain barrier

1 reference

12 December 2020

Type I glutaric aciduria, part 1: natural history of 77 patients

1 reference

12 December 2020

Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Functional and molecular identification of sodium-coupled dicarboxylate transporters in rat primary cultured cerebrocortical astrocytes and neurons

1 reference

12 December 2020

Quinolinic acid: a potent endogenous excitant at amino acid receptors in CNS

1 reference

12 December 2020

Glutaric aciduria: biochemical and morphologic considerations.

1 reference

12 December 2020

Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuria

1 reference

12 December 2020

Endothelial effects of 3-hydroxyglutaric acid: implications for glutaric aciduria type I.

1 reference

12 December 2020

Methylmalonate toxicity in primary neuronal cultures

1 reference

12 December 2020

Argininosuccinic aciduria: clinical and biochemical findings in three children with the late onset form, with special emphasis on cerebrospinal fluid findings of amino acids and pyrimidines.

1 reference

12 December 2020

Sensitivity and specificity of free and total glutaric acid and 3-hydroxyglutaric acid measurements by stable-isotope dilution assays for the diagnosis of glutaric aciduria type I

1 reference

12 December 2020

A diet-induced mouse model for glutaric aciduria type I.

1 reference

12 December 2020

Glutaryl-CoA Dehydrogenase Deficiency in Spain: Evidence of Two Groups of Patients, Genetically, and Biochemically Distinct

1 reference

12 December 2020

Cerebral dicarboxylate transport and metabolism studied with isotopically labelled fumarate, malate and malonate

1 reference

12 December 2020

10.1007/S10545-006-0415-8

Identifiers

DOI

1 reference

11 February 2018

PubMed ID

17041745

1 reference

11 February 2018