(Q49141032)

English

Chorea triggered by hyperglycemia in a maternally inherited diabetes and deafness (MIDD) patient with the A3243G mutation of mitochondrial DNA and basal ganglia calcification.

scientific article published in January 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Chorea triggered by hyperglycemia in a maternally inherited diabetes and deafness (MIDD) patient with the A3243G mutation of mitochondrial DNA and basal ganglia calcification. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

mitochondrial DNA

0 references

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Ji-Hoon Kang

1

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Sa-Yoon Kang

2

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Jay-Chol Choi

3

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Seong-Suk Lee

4

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Ji-Soo Kim

5

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

252

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

1

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

103-105

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presentation of striatal hyperintensity on T1-weighted MRI in patients with hemiballism-hemichorea caused by non-ketotic hyperglycemia: report of seven new cases and a review of literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A MERRF/PEO overlap syndrome associated with the mitochondrial DNA 3243 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MR imaging and proton MR spectroscopy in A-to-G substitution at nucleotide position 3243 of leucine transfer RNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally inherited diabetes and deafness: a new diabetes subtype

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15654564

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-005-0600-Y

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 February 2018

http://europepmc.org/abstract/MED/15654564

ResearchGate publication ID

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