Urinary excretion of C6-C10 dicarboxylic acids in glycogen storage disease types I and III

J. Dosman; J. C. Crawhall; G. A. Klassen; O. A. Mamer; P. Neumann

doi:10.1016/0009-8981(74)90065-5

Urinary excretion of C6-C10 dicarboxylic acids in glycogen storage disease types I and III

J. Dosman, J. C. Crawhall, G. A. Klassen, O. A. Mamer, P. Neumann

Research output: Contribution to journal › Article › peer-review

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Abstract

Dicarboxylic acids of chain length C6-C10 have been identified in the urine of three patients with Type I glycogen storage disease and one patient with Type III glycogen storage disease. It is suggested that the appearance of these acids in the urine is the result of inadequate gluconeogenesis with consequent alteration in the metabolic oxidative pathway of fatty acids.

Original language	English
Pages (from-to)	93-101
Number of pages	9
Journal	Clinica Chimica Acta
Volume	51
Issue number	1
DOIs	https://doi.org/10.1016/0009-8981(74)90065-5
Publication status	Published - Feb 28 1974
Externally published	Yes

Bibliographical note

Funding Information:
This work was supported by grants No. MA-3331, MA-3719 and MT-3238 from the Medical Council of Canada. The authors wish to thank Miss S.S. Tjoa for her technical assistance.

ASJC Scopus Subject Areas

Biochemistry
Clinical Biochemistry
Biochemistry, medical

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abstract = "Dicarboxylic acids of chain length C6-C10 have been identified in the urine of three patients with Type I glycogen storage disease and one patient with Type III glycogen storage disease. It is suggested that the appearance of these acids in the urine is the result of inadequate gluconeogenesis with consequent alteration in the metabolic oxidative pathway of fatty acids.",

author = "J. Dosman and Crawhall, {J. C.} and Klassen, {G. A.} and Mamer, {O. A.} and P. Neumann",

note = "Funding Information: This work was supported by grants No. MA-3331, MA-3719 and MT-3238 from the Medical Council of Canada. The authors wish to thank Miss S.S. Tjoa for her technical assistance.",

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AU - Dosman, J.

AU - Crawhall, J. C.

AU - Klassen, G. A.

AU - Mamer, O. A.

AU - Neumann, P.

N1 - Funding Information: This work was supported by grants No. MA-3331, MA-3719 and MT-3238 from the Medical Council of Canada. The authors wish to thank Miss S.S. Tjoa for her technical assistance.

PY - 1974/2/28

Y1 - 1974/2/28

N2 - Dicarboxylic acids of chain length C6-C10 have been identified in the urine of three patients with Type I glycogen storage disease and one patient with Type III glycogen storage disease. It is suggested that the appearance of these acids in the urine is the result of inadequate gluconeogenesis with consequent alteration in the metabolic oxidative pathway of fatty acids.

AB - Dicarboxylic acids of chain length C6-C10 have been identified in the urine of three patients with Type I glycogen storage disease and one patient with Type III glycogen storage disease. It is suggested that the appearance of these acids in the urine is the result of inadequate gluconeogenesis with consequent alteration in the metabolic oxidative pathway of fatty acids.

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Urinary excretion of C6-C10 dicarboxylic acids in glycogen storage disease types I and III

Abstract

Bibliographical note

ASJC Scopus Subject Areas

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