(Q48319090)

English

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case

scientific article published in August 1986

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes with acanthocytosis: a clinicopathological study of a unique case (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

lactic acidosis

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

author name string

M Mukoyama

1

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

H Kazui

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

N Sunohara

3

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

M Yoshida

4

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

I Nonaka

5

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

E Satoyoshi

6

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

publication date

1 August 1986

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

233

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

4

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

228-232

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

https://scigraph.springernature.com/pub.10.1007/bf00314025

0 references

Hereditary neurological disease with acanthocytosis. A new syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial tic disorder, parkinsonism, motor neuron disease, and acanthocytosis: a new syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondria1 encephalomyopathy with decreased succinate-cytochrome c reductase activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalomyopathies: a group of neuromuscular disorders with defects in oxidative metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular myopathy (progressive external ophthalmoplegia) with neuropathic complications

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities of erythrocytes in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics, pseudogenetics, and clinical neurology. The Robert Wartenberg Lecture.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy and cardiomyopathy with neurodegenerative features and multiple brain infarcts.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?

1 reference

https://pubmed.ncbi.nlm.nih.gov/2427665

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00314025

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/2427665

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