Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy

James E. Carroll; Beverly J. Norris; Michael H. Brooke

doi:10.1212/wnl.35.1.96

Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy

James E. Carroll, Beverly J. Norris, Michael H. Brooke

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

21 Scopus citations

Abstract

Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

Original language	English (US)
Pages (from-to)	96-97
Number of pages	2
Journal	Neurology
Volume	35
Issue number	1
DOIs	https://doi.org/10.1212/wnl.35.1.96
State	Published - Jan 1985
Externally published	Yes

ASJC Scopus subject areas

Clinical Neurology

Access to Document

10.1212/wnl.35.1.96

Cite this

@article{1d6e7cf3803940e2852c5e47e714ccb4,

title = "Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy",

abstract = "Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.",

author = "Carroll, {James E.} and Norris, {Beverly J.} and Brooke, {Michael H.}",

year = "1985",

month = jan,

doi = "10.1212/wnl.35.1.96",

language = "English (US)",

volume = "35",

pages = "96--97",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams and Wilkins",

number = "1",

}

TY - JOUR

T1 - Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy

AU - Carroll, James E.

AU - Norris, Beverly J.

AU - Brooke, Michael H.

PY - 1985/1

Y1 - 1985/1

N2 - Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

AB - Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [l-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

UR - http://www.scopus.com/inward/record.url?scp=0022004273&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0022004273&partnerID=8YFLogxK

U2 - 10.1212/wnl.35.1.96

DO - 10.1212/wnl.35.1.96

M3 - Article

C2 - 3966007

AN - SCOPUS:0022004273

SN - 0028-3878

VL - 35

SP - 96

EP - 97

JO - Neurology

JF - Neurology

IS - 1

ER -

Defective [U-14 C] palmitic acid oxidation in duchenne muscular dystrophy

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this