(Q67953219)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

title

Hereditary defect in carnitine membrane transport is expressed in skin fibroblasts (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

author name string

B O Eriksson

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

S Lindstedt

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

I Nordin

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

publication date

1 August 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

19 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

volume

147

1 reference

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19 September 2019

page(s)

662-663

1 reference

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19 September 2019

issue

6

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00442488

19 September 2019

exact match

0 references

cites work

Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transport

1 reference

12 December 2020

Primary systemic carnitine deficiency under successful therapy: clinical, biochemical, ultrahistochemical and renal clearance studies.

1 reference

12 December 2020

The syndrome of systemic carnitine deficiency: Clinical, morphologic, biochemical, and pathophysiologic features

1 reference

12 December 2020

Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome

1 reference

12 December 2020

Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome

1 reference

12 December 2020

Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00442488

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3181209%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 September 2019

0 references

1 reference