(Q61944001)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7964921%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7964921%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

main subject

mitochondrial myopathy

1 reference

3

1 reference

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29 October 2019

Alessandro Prelle

5

1 reference

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29 October 2019

Nereo Bresolin

8

1 reference

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29 October 2019

Elio Scarpini

9

1 reference

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29 October 2019

author name string

L Bet

1

1 reference

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29 October 2019

M Moggio

2

1 reference

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29 October 2019

C Mariani

4

1 reference

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29 October 2019

N Checcarelli

6

1 reference

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29 October 2019

A Bordoni

7

1 reference

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29 October 2019

G Scarlato

10

1 reference

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29 October 2019

publication date

1 July 1994

1 reference

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29 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7964921%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

volume

241

1 reference

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29 October 2019

issue

8

1 reference

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29 October 2019

page(s)

511-516

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00919714

29 October 2019

exact match

0 references

cites work

Sequence and organization of the human mitochondrial genome

1 reference

12 December 2020

Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis

1 reference

12 December 2020

Reversible alexia, mitochondrial myopathy, and lactic acidemia

1 reference

12 December 2020

Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome

1 reference

12 December 2020

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

Multiple sclerosis. Observations and reflections--a personal memoir

1 reference

12 December 2020

Rapid isolation of animal mitochondrial DNA by alkaline extraction

1 reference

12 December 2020

Mitochondrial mutations in neuro-ophthalmological diseases. A review

1 reference

12 December 2020

LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

12 December 2020

Mitochondrial DNA alterations as a source of human disorders

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.

1 reference

12 December 2020

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

1 reference

12 December 2020

A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

1 reference

12 December 2020

Detection of a specific mitochondrial DNA deletion in tissues of older humans

1 reference

12 December 2020

Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues

1 reference

12 December 2020

Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

1 reference

12 December 2020

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

1 reference

12 December 2020

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

1 reference

12 December 2020

The clinical features of mitochondrial myopathy.

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Mitochondrial DNA deletions in inherited recurrent myoglobinuria

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia.

1 reference

12 December 2020

Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy

1 reference

12 December 2020

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease

1 reference

12 December 2020

Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations

1 reference

12 December 2020

Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy

1 reference

12 December 2020

Neurological disease and mitochondrial genes

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00919714

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7964921%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 October 2019

0 references

1 reference