(Q43776338)

26 November 2017

Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands (English)

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Erratum to: Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands

26 November 2017

corrigendum / erratum

1 reference

10.1007/S10545-014-9722-7

DOI

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1007/S10545-014-9722-7

author

Olav Wendelboe Nielsen

object named as

Olav W Nielsen

2

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Lars Køber

6

object named as

Lars Køber

1 reference

26 November 2017

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Jan Rasmussen

1

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26 November 2017

Nils Janzen

3

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26 November 2017

Morten Duno

4

1 reference

26 November 2017

Hannes Gislason

5

1 reference

26 November 2017

Ulrike Steuerwald

7

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26 November 2017

Allan M Lund

8

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26 November 2017

8 May 2013

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Journal of Inherited Metabolic Disease

26 November 2017

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26 November 2017

37

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26 November 2017

2

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26 November 2017

215-222

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https://scigraph.springernature.com/pub.10.1007/s10545-013-9606-2

26 November 2017

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cites work

Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Comparison of amino acids and acylcarnitines assay methods used in newborn screening assays by tandem mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Expanded newborn screening: social and ethical issues

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Stability of acylcarnitines and free carnitine in dried blood samples: implications for retrospective diagnosis of inborn errors of metabolism and neonatal screening for carnitine transporter deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Measurement of plasma/serum acylcarnitines using tandem mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Disorders of carnitine transport and the carnitine cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Biochemical screening of 504,049 newborns in Denmark, the Faroe Islands and Greenland--experience and development of a routine program for expanded newborn screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Carnitine transporter and holocarboxylase synthetase deficiencies in The Faroe Islands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Application of electrospray tandem mass spectrometry to neonatal screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Primary carnitine deficiency and pivalic acid exposure causing encephalopathy and fatal cardiac events

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Kinetics, pharmacokinetics, and regulation of L-carnitine and acetyl-L-carnitine metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Determination of the reference range of endogenous plasma carnitines in healthy adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Accurate measurement of free carnitine in dried blood spots by isotope-dilution electrospray tandem mass spectrometry without butylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Strategies for the diagnosis of mitochondrial fatty acid beta-oxidation disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Carnitine: a nutritional, biosynthetic, and functional perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Screening newborns for inborn errors of metabolism by tandem mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Carnitine transporter defect diagnosed by newborn screening with electrospray tandem mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Linkage disequilibrium and demographic history of the isolated population of the Faroe Islands

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-013-9606-2

Increased serum carnitine concentration in renal insufficiency

21 January 2018

1 reference

12 December 2020

Carnitine transporter defect: diagnosis in asymptomatic adult women following analysis of acylcarnitines in their newborn infants

1 reference

12 December 2020

Age and sex dependency of carnitine concentration in human serum and skeletal muscle

1 reference

12 December 2020

Hereditary defect in carnitine membrane transport is expressed in skin fibroblasts

1 reference

12 December 2020

Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency

1 reference

12 December 2020

Perturbation of serum carnitine levels in human adults by chronic renal disease and dialysis therapy

1 reference

12 December 2020

Expanded newborn screening: reducing harm, assessing benefit

1 reference

12 December 2020

[Correlation of serum carnitine levels with age and sex among Chinese adults in Nanjing].

1 reference

12 December 2020

Expanded newborn screening identifies maternal primary carnitine deficiency

1 reference

12 December 2020

Acylcarnitines: analysis in plasma and whole blood using tandem mass spectrometry

1 reference

12 December 2020

Carnitine transporter deficiency in two Faeroese children

1 reference

12 December 2020

Carnitine metabolism in human subjects I. Normal metabolism,

1 reference

12 December 2020

Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessment

1 reference

12 December 2020

10.1007/S10545-013-9606-2

Identifiers

DOI

1 reference

Dimensions Publication ID

26 November 2017

0 references

1 reference