(Q51971558)

19 April 2018

title

Endocrine disorders in two sisters affected by MELAS syndrome. (English)

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19 April 2018

author name string

P Balestri

series ordinal

1

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19 April 2018

S Grosso

series ordinal

2

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19 April 2018

publication date

1 November 2000

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19 April 2018

Journal of Child Neurology

published in

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19 April 2018

volume

15

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19 April 2018

issue

11

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19 April 2018

page(s)

755-758

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19 April 2018

MELAS: clinical features, biochemistry, and molecular genetics

cites work

1 reference

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The expanding clinical spectrum of mitochondrial diseases

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Approach to diagnosis of oxidative metabolism disorders

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Hypoparathyroidism and insulin-dependent diabetes mellitus in a patient with Kearns-Sayre syndrome harbouring a mitochondrial DNA deletion.

21 January 2018

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Between and within subject variation of the first phase insulin response to intravenous glucose.

21 January 2018

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Anti-GAD65 autoantibody in Taiwanese patients with insulin-dependent diabetes mellitus: effect of HLA on anti-GAD65 positivity and clinical characteristics.

21 January 2018

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

21 January 2018

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Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001501108

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

21 January 2018

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

21 January 2018

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Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation

21 January 2018

1 reference

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Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: molecular genetic analysis and family study.

21 January 2018

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https://api.crossref.org/works/10.1177%2F088307380001501108

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

21 January 2018

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Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA.

21 January 2018

1 reference

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ATP-modulated K+ channels sensitive to antidiabetic sulfonylureas are present in adenohypophysis and are involved in growth hormone release.

21 January 2018

1 reference

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Endocrine dysfunction in Kearns-Sayre syndrome

21 January 2018

1 reference

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Autoimmune IDDM in a sporadic MELAS patient with mitochondrial tRNA(Leu(UUR)) mutation.

21 January 2018

1 reference

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10.1177/088307380001501108

21 January 2018

Identifiers

DOI

1 reference

19 April 2018

1 reference

19 April 2018