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Publications by K Bartlett

Child With a Defect in Leucine Metabolism Associated With Beta-Hydroxyisovaleric Aciduria and Beta-Methylcrotonylglycinuria.

Archives of Disease in Childhood

English

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538 Ethylmalonic-Adipic Aciduria: A New Defect of Butyrate Oxidation Associated With Hypoglycemia

Pediatric Research

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Isovaleric Acidemia: A New Genetic Defect of Leucine Metabolism.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

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Leucine Loading Test Is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH Defect

Internal Medicine

Molecular Biology

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Mapping Genetic Variants Associated With Beta-Adrenergic Responses in Inbred Mice

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A Case With Beta-Propeller Protein Associated Neurodegeneration With Smooth Response to Levodopa Treatment

Movement Disorders Clinical Practice

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Decreased Interferon Alpha/Beta Signature Associated With Human Lung Tumorigenesis

Journal of Interferon and Cytokine Research

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A Defect in Beta-Oxidation Causes Abnormal Inflorescence Development in Arabidopsis

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Mechanisms Associated With Rumpling of Pt-Modified Beta-NiAl Coatings

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The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism

American Journal of Human Genetics

English