Neutral-lipid storage disease: a new disorder of lipid metabolism.

British medical journal ·Vol. 1 ·No. 5957 ·1975-03-08 ·Pages 553-5

Chanarin I, Patel A, Slavin G, Wills EJ, Andrews TM, Stewart G

Abstract

暂无摘要

MeSH Terms

Adult Bone Marrow/pathology Carbon Radioisotopes Cells, Cultured Electromyography Female Fibroblasts/metabolism Histocytochemistry Humans Ichthyosis/etiology Intestinal Mucosa/pathology Lipid Metabolism Lipid Metabolism, Inborn Errors/blood,complications,pathology Muscles/pathology Muscular Diseases/etiology Neutrophils/metabolism Palmitic Acids/metabolism Skin/pathology

Chemicals

Carbon Radioisotopes Palmitic Acids

Authors & Affiliations

6 authors, click to expand affiliations / ORCID

Chanarin I

Patel A

Slavin G

Wills E J

Andrews T M

Stewart G

References (4)

4 references, click to expand

The familial occurrence of fat containing vacuoles in the leukocytes diagnosed in two brothers suffering from dystrophia musculorum progressiva (ERB.).
Acta Med Scand. 1953;145(6):419-23 PMID: 13079655
Jordans' anomaly in white blood cells. Report of case.
Blood. 1966 Aug;28(2):258-65 PMID: 5330405
Muscle carnitine palmityltransferase deficiency and myoglobinuria.
Science. 1973 Nov 20;182(4115):929-31 PMID: 4745596
Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome.
Science. 1973 Mar 2;179(4076):899-902 PMID: 4687787

Article Info

Journal

British medical journal

Abbr.

Br Med J

ISSN

0007-1447

DOI

10.1136/bmj.1.5957.553

Published

1975-03-08

Pages

553-5

Language

English

Region

England

NLM ID

0372673

PMCID

PMC1672681

Subset

External Links

PubMed source DOI: 10.1136/bmj.1.5957.553 PMC Full Text

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