(Q35821629)

10 August 2017

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title

Should autistic children be evaluated for mitochondrial disorders? (English)

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10 August 2017

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Esther Leshinsky-Silver

series ordinal

2

object named as

Esther Leshinsky-Silver

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Tally Lerman-Sagie

series ordinal

1

object named as

Tally Lerman-Sagie

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10 August 2017

4

Dorit Lev

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10 August 2017

3

Nathan Watemberg

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10 August 2017

publication date

1 May 2004

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Journal of Child Neurology

10 August 2017

published in

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10 August 2017

volume

19

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10 August 2017

issue

5

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10 August 2017

page(s)

379-381

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Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society

10 August 2017

cites work

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https://api.crossref.org/works/10.1177%2F088307380401900510

Identifying autism susceptibility genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

21 January 2018

The genetics of autism.

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https://api.crossref.org/works/10.1177%2F088307380401900510

Autism and lactic acidosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Infantile hypotonia as a presentation of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Autism: a mitochondrial disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Multiple presentation of mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

21 January 2018

The prevalence of autism

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Decline with age of the respiratory chain activity in human skeletal muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Biochemical studies of isolated mitochondria from normal and diseased tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

Lactic acid elevation in extramitochondrial childhood neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380401900510

10.1177/088307380401900510

21 January 2018

Identifiers

DOI

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