(Q63681442)

English

Fatal neonatal liver failure and mitochondrial cytopathy (oxidative phosphorylation deficiency): A light and electron microscopic study of the liver

scientific article published on 01 October 1993

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scholarly article

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11 October 2019

Fatal neonatal liver failure and mitochondrial cytopathy (oxidative phosphorylation deficiency): a light and electron microscopic study of the liver (English)

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8406357%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

phosphorylation

1 reference

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inferred from title

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mitochondrial myopathy

1 reference

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Valérie Cormier-Daire

8

1 reference

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11 October 2019

author name string

P Bioulac-Sage

1

1 reference

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11 October 2019

F Parrot-Roulaud

2

1 reference

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11 October 2019

J P Mazat

3

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11 October 2019

T Lamireau

4

1 reference

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11 October 2019

M Coquet

5

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11 October 2019

B Sandler

6

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11 October 2019

J L Demarquez

7

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11 October 2019

A Munnich

9

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11 October 2019

M Carré

10

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11 October 2019

language of work or name

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publication date

1 October 1993

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11 October 2019

1 reference

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11 October 2019

18

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11 October 2019

4

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11 October 2019

839-846

1 reference

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11 October 2019

Mitochondrial DNA mutations and neuromuscular disease

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

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Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical aspects of mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Fatal neonatal hepatocellular deficiency with lactic acidosis: a defect of the respiratory chain

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Hepatic failure in disorders of oxidative phosphorylation with neonatal onset

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Fatal neonatal liver failure and mitochondrial cytopathy: an observation with antenatal ascites

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Fatal infantile liver failure associated with mitochondrial DNA depletion

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial phosphoenolpyruvate carboxykinase deficiency.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Medium-chain acyl CoA dehydrogenase deficiency: electron microscopic differentiation from Reye syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Valproate use associated with persistent hyperammonemia and mitochondrial injury in a child with Down's syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Infantile Diffuse Cerebral Degeneration With Hepatic Cirrhosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Liver involvement in Alpers disease.

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Subacute necrotizing encephalomyelopathy in an infant

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Idiopathic neonatal iron storage involving the liver, pancreas, heart, and endocrine and exocrine glands

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Neonatal hemochromatosis

1 reference

https://api.crossref.org/works/10.1002%2FHEP.1840180414

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HEP.1840180414

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8406357%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8406357%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

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