(Q35124267)

6 August 2017

1 reference

title

Abnormalities in gastrointestinal motility are associated with diseases of oxidative phosphorylation in children (English)

1 reference

6 August 2017

1 reference

2

Samuel Nurko

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12738470

31 December 2023

author name string

Timothy Buie

4

1 reference

6 August 2017

Alejandro Flores

5

1 reference

6 August 2017

Denesh K. Chitkara

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12738470

31 December 2023

John M. Shoffner

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12738470

31 December 2023

language of work or name

English

0 references

publication date

1 April 2003

1 reference

full work available at URL

6 August 2017

https://journals.lww.com/10.1111/j.1572-0241.2003.07385.x

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

The American Journal of Gastroenterology

31 December 2023

published in

1 reference

6 August 2017

volume

98

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6 August 2017

issue

4

1 reference

6 August 2017

page(s)

871-877

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Maternal inheritance and the evaluation of oxidative phosphorylation diseases

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2003.07385.X

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2003.07385.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2003.07385.X

Effect of sequential erythromycin and octreotide on antroduodenal manometry.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2003.07385.X

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2003.07385.X

Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2003.07385.X

Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2003.07385.X

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

21 January 2018

3

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Familial occurrence of intestinal obstruction in children with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)

31 December 2023

4

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations

31 December 2023

5

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Chronic intestinal pseudoobstruction and ophthalmoplegia in a patient with mitochondrial myopathy

31 December 2023

6

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorder

31 December 2023

7

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Mitochondrial neurogastrointestinal encephalomyopathy: manometric and diagnostic features

31 December 2023

8

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

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

31 December 2023

10

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV.

31 December 2023

11

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

31 December 2023

Mitochondrial medicine

13

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Mitochondrial Neurogastrointestinal Encephalomyopathy

31 December 2023

15

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

A novel mitochondrial G8313A mutation associated with prominent initial gastrointestinal symptoms and progressive encephaloneuropathy

31 December 2023

16

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.

31 December 2023

17

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?

31 December 2023

19

1 reference

https://api.crossref.org/works/10.1111/J.1572-0241.2003.07385.X

31 December 2023

Identifiers

1 reference

6 August 2017

1 reference