18Fluoro-2-deoxyglucose (18FDG) PET scan of the brain in type IV 3-methylglutaconic aciduria: clinical and MRI correlations. (Q48260632)

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12 November 2019

title

18Fluoro-2-deoxyglucose (18FDG) PET scan of the brain in type IV 3-methylglutaconic aciduria: clinical and MRI correlations (English)

1 reference

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3-methylglutaconic aciduria

12 November 2019

main subject

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4

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12 November 2019

author name string

M Al-Essa

1

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12 November 2019

S Bakheet

2

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12 November 2019

L Al-Shamsan

3

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12 November 2019

J Powe

5

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12 November 2019

P T Ozand

6

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12 November 2019

publication date

1 January 1999

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12 November 2019

published in

Brain and Development

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12 November 2019

volume

21

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12 November 2019

issue

1

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12 November 2019

page(s)

24-29

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3-Methylglutaconic aciduria: a marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a 'new' type ('type 4')

12 November 2019

cites work

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Multiple syndromes of 3-methylglutaconic aciduria

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3-Methylglutaconic aciduria: ten new cases with a possible new phenotype.

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Inherited 3-methylglutaconic aciduria in two brothers—Another defect of leucine metabolism

1 reference

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7 January 2021

Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria

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7 January 2021

3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case

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3-Methylglutaconic and 3-methylglutaric aciduria in a patient with suspected 3-methylglutaconyl-CoA hydratase deficiency

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X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

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7 January 2021

3-methylglutaconic aciduria: report on a sibship with infantile progressive encephalopathy

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7 January 2021

Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria

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3-Methylglutaconic aciduria in two infants

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3-Methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism

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3-Methylglutaconic aciduria in "optic atrophy plus".

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Behr's syndrome and 3-methylglutaconic aciduria

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Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria

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7 January 2021

3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects

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7 January 2021

Quantification of 3-methylglutaconic acid in urine, plasma, and amniotic fluid by isotope-dilution gas chromatography/mass spectrometry

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7 January 2021

CT and MR of the brain in the diagnosis of organic acidemias. Experiences from 107 patients

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7 January 2021

Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria

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7 January 2021

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria

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7 January 2021

10.1016/S0387-7604(98)00064-3

Identifiers

DOI

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12 November 2019

1 reference