Systemic carnitine deficiency. Report of a fatal case with multisystemic manifestations (Q67418623)

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13 September 2019

title

Systemic carnitine deficiency. Report of a fatal case with multisystemic manifestations (English)

1 reference

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13 September 2019

author name string

A. J. Ware

1

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23 July 2022

W. C. Burton

2

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23 July 2022

J. D. McGarry

3

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23 July 2022

J. F. Marks

4

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23 July 2022

A. G. Weinberg

5

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23 July 2022

language of work or name

English

0 references

publication date

1 December 1978

1 reference

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The Journal of Pediatrics

13 September 2019

published in

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13 September 2019

volume

93

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13 September 2019

issue

6

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13 September 2019

page(s)

959-964

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Fatal systemic carnitine deficiency with lipid storage in skeletal muscle, heart, liver and kidney

13 September 2019

cites work

1 reference

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Fatal cases of lipid storage myopathy with carnitine deficiency

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Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case

7 January 2021

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Lipid storage myopathy responsive to prednisone

7 January 2021

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

7 January 2021

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

7 January 2021

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Muscle carnitine deficiency. Association with lipid myopathy, vacuolar neuropathy, and vacuolated leukocytes

7 January 2021

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Hereditary carnitine deficiency of muscle

7 January 2021

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Letter: Inborn error of carnitine metabolism ("carnitine deficiency") in man

7 January 2021

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Letter: Carnitine deficiency

7 January 2021

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Carnitine deficiency of skeletal muscle: report of a treated case

7 January 2021

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Jamaican vomiting sickness. Biochemical investigation of two cases

7 January 2021

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Metabolic effects of hypoglycin and methylenecyclopropaneacetic acid

7 January 2021

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Hepatitis-associated lipid storage myopathy

7 January 2021

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

7 January 2021

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A Skeletal-Muscle Disorder Associated with Intermittent Symptoms and a Possible Defect of Lipid Metabolism

7 January 2021

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Muscle Carnitine Palmityltransferase Deficiency and Myoglobinuria

7 January 2021

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Partial Deficiency of Muscle Carnitine Palmitoyltransferase with Normal Ketone Production

7 January 2021

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Lipid storage myopathy with normal carnitine levels

7 January 2021

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BIOCHEMICAL LESION OF DIPHTHERIA TOXIN IN THE HEART.

7 January 2021

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Oral treatment of carnitine myopathy

7 January 2021

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10.1016/S0022-3476(78)81219-0

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:722440%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

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