(Q36315564)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

review article

1 reference

title

Digestive smooth muscle mitochondrial myopathy in patients with mitochondrial-neuro-gastro-intestinal encephalomyopathy (MNGIE) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

main subject

mitochondrial myopathy

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Hugues Blondon

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Marc Polivka

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Francisca Joly

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Jacqueline Mikol

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Bernard Messing

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

publication date

1 August 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

Gastroenterologie Clinique et Biologique

9 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

8-9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

page(s)

773-778

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

Inherited ophthalmoplegia with intestinal pseudo-obstruction

9 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Late-onset oculogastrointestinal muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Familial intestinal pseudoobstruction dominated by a progressive neurologic disease at a young age.

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Familial progressive neuronal disease and chronic idiopathic intestinal pseudo-obstruction.

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Chronic intestinal pseudoobstruction and ophthalmoplegia in a patient with mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudo-obstruction: POLIP syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 12-1990. A 21-year-old man with progressive gastrointestinal stasis, hepatomegaly, and a neurologic disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Ophthalmoplegia, demyelinating neuropathy, leukoencephalopathy, myopathy, and gastrointestinal dysfunction with multiple deletions of mitochondrial DNA: a mitochondrial multisystem disorder in search of a name

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Ophthalmic involvement in myo-neuro-gastrointestinal encephalopathy syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Multiple mitochondrial DNA deletions in myo-neuro-gastrointestinal encephalopathy syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Familial visceral myopathy associated with a mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Mitochondrial Neurogastrointestinal Encephalomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Phenotypic variability in a Spanish family with MNGIE.

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Neuronal intranuclear inclusion disease in a child: diagnosis by rectal biopsy

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Familial visceral neuropathy with neuronal intranuclear inclusions: Diagnosis by rectal biopsy

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Mitochondrial neurogastrointestinal encephalomyopathy: manometric and diagnostic features

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Mitochondrial respiratory-chain diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Altered thymidine metabolism due to defects of thymidine phosphorylase

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0399-8320%2805%2986346-8

7 January 2021

10.1016/S0399-8320(05)86346-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16294144%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference