(Q67271350)

English

Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle

scientific article published on 01 January 1983

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

myopathy with abnormal lipid metabolism

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

author name string

J Müller-Höcker

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

D Pongratz

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

J M Trijbels

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

W Endres

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

G Hübner

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

publication date

1 January 1983

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

Virchows Archiv. A, Pathological Anatomy and Histopathology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

399

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

11-23

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

Fatal cases of lipid storage myopathy with carnitine deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electron microscopic observations in thyrotoxic and corticosteroid-induced myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent Hypoglycemia Associated with Glutaric Aciduria Type II in an Adult

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morphological features in a neutral lipid storage disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Successful carnitine treatment in a non-carnitine-deficient lipid storage myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine "deficiency": lack of response to carnitine therapy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of ethidium bromide on the cytochrome content and ultrastructure of L cell mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Experimental lipid storage myopathy. A quantitative ultrastructural and biochemical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

INDUCTION OF SWELLING OF LIVER MITOCHONDRIA BY FATTY ACIDS OF VARIOUS CHAIN LENGTH

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid storage myopathy with normal carnitine levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disorders of lipid metabolism in muscle.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro analysis of hepatic carnitine biosynthesis in human systemic carnitine deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid storage myopathy, ichthyosis, and steatorrhea

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle carnitine deficiency. Genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of lipid droplets in human skeletal muscle in neuromuscular disorders: a histochemical, electron-microscopic and freeze-etch study

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The syndrome of carnitine deficiency: morphological and metabolic correlations in two cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipid storage myopathies. A review of metabolic defect and of treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial carnitine deficiency. A fatal case and subclinical state in a sister

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of glutaraldehyde on catalase. Biochemical and cytochemical studies with beef liver catalase and rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine deficiency induced during intermittent haemodialysis for renal failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myopathy associated with pigmentation following adrenalectomy for Cushing's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine palmitoyltransferase II deficiency with normal carnitine palmitoyltransferase I in skeletal muscle and leucocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle carnitine deficiency and fatal cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine deficiency in premature infants receiving total parenteral nutrition

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low carnitine levels in serum of pregnant women

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of carnitine in cachectic cirrhotic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uncoupling activity of long-chain fatty acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Sudanophilic (mitochondria) myopathy (author's transl)].

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructural features of intracellular lipid in normal human muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuromuscular disorders with abnormal muscle mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal lipid storage myopathy in an infant: case report and autopsy findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine levels in normal children and adults and in patients with diseases muscle.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased tissue carnitine concentrations in newborn infants receiving total parenteral nutrition

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Case of Metabolic Mimicry

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular carnitine synthesis and palmitate metabolism in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Letter: A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/6298999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00666215

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6298999%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q67271350&oldid=2172022560"