(Q73760642)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10801057%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Multiple mtDNA deletions: clinical and molecular correlations (English)

1 reference

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6 November 2019

5

1 reference

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6 November 2019

Lucio Santoro

9

1 reference

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6 November 2019

Filippo Maria Santorelli

object named as

F M Santorelli

1

1 reference

ORCID Public Data File 2021

author name string

G De Joanna

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10801057%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

C Casali

3

1 reference

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6 November 2019

A Tessa

4

1 reference

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6 November 2019

G A Amabile

6

1 reference

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6 November 2019

F Pierelli

7

1 reference

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6 November 2019

L Vilarinho

8

1 reference

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6 November 2019

publication date

1 March 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10801057%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

6 November 2019

published in

1 reference

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6 November 2019

volume

23

1 reference

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6 November 2019

issue

2

1 reference

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6 November 2019

page(s)

155-161

1 reference

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Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy

6 November 2019

cites work

1 reference

12 December 2020

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

1 reference

12 December 2020

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

1 reference

12 December 2020

Disorders of nuclear-mitochondrial intergenomic signalling.

1 reference

12 December 2020

Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia

1 reference

12 December 2020

Increased prevalence of mitochondrial DNA deletions in skeletal muscle of older individuals with impaired glucose tolerance: possible marker of glycemic stress

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients

1 reference

12 December 2020