(Q50302132)

English

Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene

scientific article published in November 2006

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

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1 reference

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inferred from title

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Manuela Grazina

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Astrid M. Vicente

12

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Catarina Correia

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Catarina Correia

1

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Guiomar Oliveira

object named as

Guiomar Oliveira

11

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Catarina R. Oliveira

object named as

Catarina Oliveira

10

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author name string

Ana M Coutinho

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Carla Marques

5

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Teresa Miguel

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Assunção Ataíde

7

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Joana Almeida

8

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Luís Borges

9

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

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publication date

1 November 2006

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

36

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

8

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

1137-1140

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

Mitochondrial dysfunction in autistic patients with 15q inverted duplication

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum serotonin, lactate and pyruvate levels in infantile autistic children

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA abnormalities and autistic spectrum disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic criteria for respiratory chain disorders in adults and children.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism: a mitochondrial disorder?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial dysfunction in autism spectrum disorders: a population-based study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of altered energy metabolism in autistic children

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of austim: complex aetiology for a heterogeneous disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Citrin and aralar1 are Ca(2+)-stimulated aspartate/glutamate transporters in mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/17151801

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10803-006-0138-6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/17151801

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