Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children : an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years. / Banner, Jytte; Kølvraa, S; Gregersen, N; Christensen, Erik; Gregersen, M.

I: Journal of Clinical Pathology, Bind 50, Nr. 4, 08.1997, s. 212-7.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Banner, J, Kølvraa, S, Gregersen, N, Christensen, E & Gregersen, M 1997, 'Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years', Journal of Clinical Pathology, bind 50, nr. 4, s. 212-7.

APA

Banner, J., Kølvraa, S., Gregersen, N., Christensen, E., & Gregersen, M. (1997). Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years. Journal of Clinical Pathology, 50(4), 212-7.

Vancouver

Banner J, Kølvraa S, Gregersen N, Christensen E, Gregersen M. Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years. Journal of Clinical Pathology. 1997 aug;50(4):212-7.

Author

Banner, Jytte ; Kølvraa, S ; Gregersen, N ; Christensen, Erik ; Gregersen, M. / Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children : an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years. I: Journal of Clinical Pathology. 1997 ; Bind 50, Nr. 4. s. 212-7.

Bibtex

@article{3e8b7ccb44cc42e6853cd7ebad69759a,
title = "Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years",
abstract = "Disorders of fatty acid metabolism are known to be responsible for cases of sudden and unexpected death in infancy. At least 14 disorders are known at present. 120 cases of sudden infant death syndrome (SIDS) had been examined for a prevalent mutation (G985) causing medium chain acyl CoA dehydrogenase deficiency, which is inherited in an autosomal recessive mode. No over-representation of either homozygous or heterozygous cases was found.",
keywords = "Acyl-CoA Dehydrogenase, Acyl-CoA Dehydrogenases, Cell Culture Techniques, Child, Preschool, Fatty Acids, Female, Fibroblasts, Heterozygote, Humans, Infant, Infant, Newborn, Lipid Metabolism, Inborn Errors, Male, Oxidation-Reduction, Point Mutation, Prospective Studies, Sudden Infant Death",
author = "Jytte Banner and S K{\o}lvraa and N Gregersen and Erik Christensen and M Gregersen",
year = "1997",
month = "8",
language = "English",
volume = "50",
pages = "212--7",
journal = "Journal of Clinical Pathology",
issn = "0021-9746",
publisher = "B M J Group",
number = "4",

}

RIS

TY - JOUR

T1 - Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children

T2 - an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years

AU - Banner, Jytte

AU - Kølvraa, S

AU - Gregersen, N

AU - Christensen, Erik

AU - Gregersen, M

PY - 1997/8

Y1 - 1997/8

N2 - Disorders of fatty acid metabolism are known to be responsible for cases of sudden and unexpected death in infancy. At least 14 disorders are known at present. 120 cases of sudden infant death syndrome (SIDS) had been examined for a prevalent mutation (G985) causing medium chain acyl CoA dehydrogenase deficiency, which is inherited in an autosomal recessive mode. No over-representation of either homozygous or heterozygous cases was found.

AB - Disorders of fatty acid metabolism are known to be responsible for cases of sudden and unexpected death in infancy. At least 14 disorders are known at present. 120 cases of sudden infant death syndrome (SIDS) had been examined for a prevalent mutation (G985) causing medium chain acyl CoA dehydrogenase deficiency, which is inherited in an autosomal recessive mode. No over-representation of either homozygous or heterozygous cases was found.

KW - Acyl-CoA Dehydrogenase

KW - Acyl-CoA Dehydrogenases

KW - Cell Culture Techniques

KW - Child, Preschool

KW - Fatty Acids

KW - Female

KW - Fibroblasts

KW - Heterozygote

KW - Humans

KW - Infant

KW - Infant, Newborn

KW - Lipid Metabolism, Inborn Errors

KW - Male

KW - Oxidation-Reduction

KW - Point Mutation

KW - Prospective Studies

KW - Sudden Infant Death

M3 - Journal article

C2 - 9350306

VL - 50

SP - 212

EP - 217

JO - Journal of Clinical Pathology

JF - Journal of Clinical Pathology

SN - 0021-9746

IS - 4

ER -

ID: 46809982