Redefining phenotypes associated with mitochondrial DNA single deletion (Q39025384)

8 September 2017

Redefining phenotypes associated with mitochondrial DNA single deletion (English)

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Erratum to: Redefining phenotypes associated with mitochondrial DNA single deletion

8 September 2017

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corrigendum / erratum

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author

Corrado Angelini

3

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8 September 2017

6

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8 September 2017

Donato Sauchelli

28

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Elena Caldarazzo Ienco

Elena Caldarazzo Ienco

18

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Michelangelo Mancuso

Michelangelo Mancuso

1

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Dario Ronchi

Dario Ronchi

27

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Luca Bello

Luca Bello

17

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Maria Lucia Valentino

Maria Lucia Valentino

31

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Valerio Carelli

Valerio Carelli

5

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Gabriele Siciliano

Gabriele Siciliano

34

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Enrico Bertini

Enrico Bertini

4

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Antonio Federico

Antonio Federico

8

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Massimo Zeviani

33

Massimo Zeviani

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8 September 2017

23

Costanza Lamperti

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8 September 2017

24

Isabella Moroni

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8 September 2017

10

Maurizio Moggio

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8 September 2017

30

Monica Sciacco

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8 September 2017

11

Tiziana Mongini

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8 September 2017

Filippo Maria Santorelli

Filippo Maria Santorelli

12

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ORCID Public Data File 2021

author name string

Daniele Orsucci

2

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8 September 2017

Maria Alice Donati

7

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8 September 2017

Carlo Minetti

9

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8 September 2017

Serenella Servidei

13

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Paola Tonin

14

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Antonio Toscano

15

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8 September 2017

Claudio Bruno

16

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Elena Cardaioli

19

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Michela Catteruccia

20

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Paola Da Pozzo

21

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Massimiliano Filosto

22

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Olimpia Musumeci

25

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8 September 2017

Elena Pegoraro

26

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8 September 2017

Mauro Scarpelli

29

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Liliana Vercelli

32

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8 September 2017

26 March 2015

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8 September 2017

262

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8 September 2017

1301-1309

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8 September 2017

5

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describes a project that uses

8 September 2017

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https://scigraph.springernature.com/pub.10.1007/s00415-015-7710-y

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cites work

Mitochondrial respiratory-chain diseases

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Mitochondrial diseases: a nosological update.

21 January 2018

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Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Diagnostic criteria for respiratory chain disorders in adults and children.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Single deletions in mitochondrial DNA--molecular mechanisms and disease phenotypes in clinical practice

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Prevalence of mitochondrial DNA disease in adults

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Pearson's marrow/pancreas syndrome: a histological and genetic study

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Mitochondrial DNA single deletion in a patient with postural tremor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Mitochondrial DNA analysis in ocular myopathy. Observations in 29 Portuguese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Disease progression in patients with single, large-scale mitochondrial DNA deletions

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Diagnostic approach to mitochondrial disorders: the need for a reliable biomarker.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Neuropathology of mitochondrial diseases

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-015-7710-Y

CPEO and KSS differ in the percentage and location of the mtDNA deletion

21 January 2018

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12 December 2020

Ocular myopathy and mitochondrial DNA deletion. A presentation of seven identified Danish patients.

1 reference

12 December 2020

New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle

1 reference

12 December 2020

Single large-scale mitochondrial DNA deletion in a patient with mitochondrial myopathy associated with multiple symmetric lipomatosis

1 reference

12 December 2020

Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease

1 reference

12 December 2020

Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia

1 reference

12 December 2020

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

12 December 2020

Leigh-type neuropathology in Pearson syndrome associated with impaired ATP production and a novel mtDNA deletion

1 reference

12 December 2020

10.1007/S00415-015-7710-Y

Identifiers

DOI

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8 September 2017

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