(Q50507495)

14 March 2018

title

Psychiatric symptoms in a patient with diabetes mellitus associated with point mutation in mitochondrial DNA. (English)

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14 March 2018

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Inagaki T

1

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14 March 2018

Ishino H

2

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14 March 2018

Seno H

3

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14 March 2018

Ohguni S

4

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14 March 2018

Tanaka J

5

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14 March 2018

Kato Y

6

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14 March 2018

language of work or name

English

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publication date

1 December 1997

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14 March 2018

published in

Biological Psychiatry

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14 March 2018

volume

42

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14 March 2018

issue

11

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14 March 2018

page(s)

1067-1069

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14 March 2018

A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Mitochondrial encephalomyopathy (MELAS): pathological study and successful therapy with coenzyme Q10 and idebenone

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Idebenone improves cerebral mitochondrial oxidative metabolism in a patient with MELAS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Deletion of leukocyte mitochondrial DNA in bipolar disorder

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Decreased cerebral blood perfusion in an NIDDM patient with an A-to-G mutation in the mitochondrial gene; a possible contribution to cognition deficits in diabetes mellitus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Mitochondrial encephalomyopathy (MELAS) with mental disorder. CT, MRI and SPECT findings

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Mitochondrial encephalomyopathy: fluctuating symptoms and CT.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900351-X

10.1016/S0006-3223(97)00351-X

7 January 2021

Identifiers

DOI

1 reference

14 March 2018

PubMed ID

9386859

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14 March 2018