(Q48163470)

9 February 2018

title

Defects in muscle fiber growth in fatal infantile cytochrome c oxidase deficiency (English)

1 reference

9 February 2018

author name string

Nonaka I

1

1 reference

9 February 2018

Koga Y

2

1 reference

9 February 2018

Okino E

3

1 reference

9 February 2018

Kikuchi A

4

1 reference

9 February 2018

Fujisawa K

5

1 reference

9 February 2018

Miyabayashi S

6

1 reference

9 February 2018

publication date

1 January 1988

1 reference

9 February 2018

published in

Brain and Development

1 reference

9 February 2018

volume

10

1 reference

9 February 2018

issue

4

1 reference

9 February 2018

page(s)

223-230

1 reference

9 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Cytochrome-c-oxidase deficiency in a floppy infant

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

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/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Cytochrome C oxidase deficiency in two siblings with leigh encephalomyelopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Benign reversible muscle cytochrome c oxidase deficiency: a second case

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Multiple cytochrome deficiency and deteriorated mitochondrial polypeptide composition in fatal infantile mitochondrial myopathy and renal dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Muscle fibre type differentiation and satellite cell population in Werdnig-Hoffmann disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Electron microscopic observations of satellite cells with special reference to the development of mammalian skeletal muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Fetal muscle characteristics in nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

Reincarnation in cultured muscle of mitochondrial abnormalities. Two patients with epilepsy and lactic acidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2888%2980002-0

7 January 2021

10.1016/S0387-7604(88)80002-0

Identifiers

DOI

0 references

1 reference

9 February 2018