(Q72351984)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Recurrent respiratory failure in a patient with 3243 mutation in mitochondrial DNA (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

K Kamakura

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

H Abe

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

Y Tadano

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

R Nakamura

4

1 reference

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26 October 2019

H Kobayashi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

S Kawaguchi

6

1 reference

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26 October 2019

N Nagata

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

T Matsuoka

8

1 reference

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26 October 2019

R Sakuta

9

1 reference

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26 October 2019

I Nonaka

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

publication date

1 March 1995

1 reference

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26 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

242

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

issue

4

1 reference

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26 October 2019

page(s)

253-255

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00919602

26 October 2019

exact match

0 references

cites work

Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

1 reference

12 December 2020

Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations

1 reference

12 December 2020

Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics

1 reference

12 December 2020

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy

1 reference

12 December 2020

Respiratory failure revealing mitochondrial myopathy in adults

1 reference

12 December 2020

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00919602

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798128%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference