Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.

Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.

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Q46720533

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Metabonomic analysis of HIV-infected biofluids.Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.

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Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.

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2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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Quantitative acylcarnitine pro ...... on and organic acid disorders.

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Quantitative acylcarnitine pro ...... on and organic acid disorders.

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Quantitative acylcarnitine pro ...... on and organic acid disorders.

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Quantitative acylcarnitine pro ...... on and organic acid disorders.

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Quantitative acylcarnitine pro ...... on and organic acid disorders.

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Quantitative acylcarnitine pro ...... on and organic acid disorders.

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Andrea Schulze-Bergkamen

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Cheryl R Greenberg

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Dirk Kohlmüller

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Dorothea Haas

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Ertan Mayatepek

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Georg F Hoffmann

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Henning Schulze-Bergkamen

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Johannes Zschocke

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Jürgen G Okun

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Martin Lindner

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P2860

Disorders of mitochondrial fatty acyl-CoA beta-oxidation

Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder

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

Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship

Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that res

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

Evaluation of urinary acylglycines by electrospray tandem mass spectrometry in mitochondrial energy metabolism defects and organic acidurias.

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients.

Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implications.

Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns.

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2005-09-23T00:00:00Z

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Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.

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P2860

P2860

Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.

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