(Q72860652)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

Rapid and noninvasive screening of patients with mitochondrial myopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

main subject

mitochondrial myopathy

1 reference

Kotsimbos N

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Jean-Francois MJ

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Huizing M

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Kapsa RM

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Lertrit P

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Siregar NC

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Marzuki S

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Sue C

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Byrne E

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

publication date

1 January 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

volume

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

page(s)

132-135

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

MELAS: clinical features, biochemistry, and molecular genetics

29 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

DNA typing from single hairs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

Noninvasive diagnosis of the MELAS syndrome from blood DNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380040207

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380040207

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7981717%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference