(Q34505872)

2 August 2017

Developmental regression and mitochondrial dysfunction in a child with autism (English)

1 reference

2 August 2017

0 references

developmental regression

1 reference

1 reference

Jon S Poling

1

1 reference

2 August 2017

Richard E Frye

series ordinal

2

1 reference

2 August 2017

John Shoffner

series ordinal

3

1 reference

2 August 2017

Andrew W Zimmerman

series ordinal

4

1 reference

2 August 2017

language of work or name

1 reference

1 February 2006

1 reference

Journal of Child Neurology

2 August 2017

1 reference

2 August 2017

21

1 reference

2 August 2017

2

1 reference

2 August 2017

170-172

1 reference

Developmental regression in autism spectrum disorders

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

Should autistic children be evaluated for mitochondrial disorders?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

Neuropathology of Rett syndrome: case report with neuronal and mitochondrial abnormalities in the brain

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

Mitochondrial DNA abnormalities and autistic spectrum disorders.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

Mitochondrial dysfunction in autistic patients with 15q inverted duplication

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

Infantile hypotonia as a presentation of Rett syndrome.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2536523

Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16566887

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1177/08830738060210021401

1 reference

2 August 2017

1 reference

2 August 2017

1 reference