(Q46391307)

English

Magnetic resonance imaging in MELAS syndrome

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

Magnetic resonance imaging in MELAS syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

author name string

L Rosen

1

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

S Phillips

2

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

D Enzmann

3

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

publication date

1 January 1990

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

32

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

2

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

168-171

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

https://scigraph.springernature.com/pub.10.1007/bf00588572

0 references

Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalomyopathy: fluctuating symptoms and CT.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

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/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

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/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial encephalopathy, lactic acidosis, and strokelike syndrome (MELAS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

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/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Computed tomography and angiography in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes); report of 3 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

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/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

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/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MELAS syndrome involving a mother and two children

1 reference

https://pubmed.ncbi.nlm.nih.gov/2398945

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/2398945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00588572

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/2398945

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