(Q38257315)

1 September 2017

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title

Zellweger syndrome and secondary mitochondrial myopathy (English)

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1 September 2017

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Vincenzo Salpietro

1

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Martino Ruggieri

object named as

Martino Ruggieri

9

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author name string

Rahul Phadke

2

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1 September 2017

Anand Saggar

3

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1 September 2017

Iain P Hargreaves

4

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1 September 2017

Robert Yates

5

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1 September 2017

Christos Fokoloros

6

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1 September 2017

Kshitij Mankad

7

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1 September 2017

Jozef Hertecant

8

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1 September 2017

David McCormick

10

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1 September 2017

Maria Kinali

11

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1 September 2017

publication date

7 October 2014

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European Journal of Pediatrics

1 September 2017

published in

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1 September 2017

volume

174

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1 September 2017

issue

4

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1 September 2017

page(s)

557-563

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https://scigraph.springernature.com/pub.10.1007/s00431-014-2431-2

1 September 2017

exact match

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cites work

A new autosomal recessive syndrome with Zellweger-like manifestations.

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Mitochondrial disease: a practical approach for primary care physicians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Inhibition of mitochondrial complex IV leads to secondary loss complex II-III activity: implications for the pathogenesis and treatment of mitochondrial encephalomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Amyotrophic lateral sclerosis with ragged-red fibers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Rotenone-like action of the branched-chain phytanic acid induces oxidative stress in mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-014-2431-2

Mitochondrial dysfunction in neuromuscular disorders

21 January 2018

1 reference

12 December 2020

Peroxisome biogenesis disorders: molecular basis for impaired peroxisomal membrane assembly: in metabolic functions and biogenesis of peroxisomes in health and disease

1 reference

12 December 2020

Neurodegeneration in methylmalonic aciduria involves inhibition of complex II and the tricarboxylic acid cycle, and synergistically acting excitotoxicity

1 reference

12 December 2020

Mitochondrial damage: an important feature in a number of inborn errors of metabolism?

1 reference

12 December 2020

Mitochondrial myopathy with loosely coupled oxidative phosphorylation in a case of Zellweger syndrome. A cytochemical-ultrastructural study.

1 reference

12 December 2020

Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease

1 reference

12 December 2020

Mitochondrial myopathy of cerebro-hepato-renal (Zellweger) syndrome.

1 reference

12 December 2020

10.1007/S00431-014-2431-2

Identifiers

DOI

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Dimensions Publication ID

1 September 2017

1018189820

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