(Q74570537)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

Possible role of mtDNA mutations in sudden infant death (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

author name string

Siri H Opdal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Ashild Vege

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Thore Egeland

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Musse A Musse

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Torleiv O Rognum

5

1 reference

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11 November 2019

publication date

1 July 2002

1 reference

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11 November 2019

1 reference

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11 November 2019

volume

27

1 reference

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11 November 2019

issue

1

1 reference

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11 November 2019

page(s)

23-29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

Use of new Nordic criteria for classification of SIDS to re-evaluate diagnoses of sudden unexpected infant death in the Nordic countries

11 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Risk of sudden infant death syndrome in subsequent siblings

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Population-based recurrence risk of sudden infant death syndrome compared with other infant and fetal deaths

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

SIDS--changes in the epidemiological pattern in eastern Norway 1984-1996.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Recurrence incidence of sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

The predictive value of behavioural risk factors for sudden infant death.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

An assessment of behavioural characteristics in infants who died of sudden infant death syndrome using the Early Infancy Temperament Questionnaire.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Mitochondrial DNA sequences for 118 individuals from northeastern Spain

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Diseases caused by nuclear genes affecting mtDNA stability

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Up-regulated epithelial expression of HLA-DR and secretory component in salivary glands: reflection of mucosal immunostimulation in sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

SIDS cases have increased levels of interleukin-6 in cerebrospinal fluid

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Factors potentiating the risk of sudden infant death syndrome associated with the prone position.

1 reference

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7 January 2021

The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

The ND1 T3308C mutation may be a mtDNA polymorphism. Report of two Portuguese patients

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

About the "Pathological" role of the mtDNA T3308C mutationellipsis

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Strand asymmetry in human mitochondrial DNA mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

Subunit III of cytochrome c oxidase is not involved in proton translocation: a site-directed mutagenesis study

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2802%2900384-3

7 January 2021

10.1016/S0887-8994(02)00384-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12160969%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference