(Q72877445)

English

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)

scientific article published on 01 August 1994

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7988784%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7988784%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

mitochondrial encephalomyopathy

1 reference

based on heuristic

inferred from title

lactic acidosis

1 reference

based on heuristic

inferred from title

author name string

S Suzuki

1

1 reference

Europe PubMed Central

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30 October 2019

Y Hinokio

2

1 reference

Europe PubMed Central

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30 October 2019

S Hirai

3

1 reference

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30 October 2019

M Onoda

4

1 reference

Europe PubMed Central

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30 October 2019

M Matsumoto

5

1 reference

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30 October 2019

M Ohtomo

6

1 reference

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30 October 2019

H Kawasaki

7

1 reference

Europe PubMed Central

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30 October 2019

Y Satoh

8

1 reference

Europe PubMed Central

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30 October 2019

H Akai

9

1 reference

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30 October 2019

K Abe

10

1 reference

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30 October 2019

publication date

1 August 1994

1 reference

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30 October 2019

1 reference

Europe PubMed Central

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30 October 2019

37

1 reference

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30 October 2019

818-825

1 reference

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30 October 2019

8

1 reference

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30 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00404339

0 references

Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kearns-Sayre syndrome: the importance of early recognition

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does autonomic neuropathy in diabetes cause hearing deficits?

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of mitochondrial gene mutations in families with diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impairment of the mitochondrial oxidative response to D-glucose in pancreatic islets from adult rats injected with streptozotocin during the neonatal period

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oculocraniosomatic neuromuscular disease with hypoparathyroidism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypothalamic GH Deficiency and gelastic seizures in a 10-year-old girl with MELAS

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disorder of the inner ear in diabetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Evaluation of hearing in patients with diabetes].

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new type of mitochondrial DNA deletion in patients with encephalomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac involvement in mitochondrial disease: a clinical study of 38 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial gene mutations and diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive ocular myopathy with ovarian insufficiency and diabetes mellitus. Report of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peripheral neuropathy of mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abrupt neurological deterioration in children with Kearns-Sayre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the 64K autoantigen in insulin-dependent diabetes as the GABA-synthesizing enzyme glutamic acid decarboxylase

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autoantibodies to 64,000-M(r) islet cell protein in long-term type 1 (insulin-dependent) diabetic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and pathogenic significance of pancreatic-islet-cell antibodies in diabetics treated with oral hypoglycaemic agents

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetes mellitus in Kearns-Sayre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial gene mutations and diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MYOPATHIC DISORDER ASSOCIATED WITH MITOCHONDRIAL ABNORMALITIES, HYPERGLYCÆMIA, AND HYPERKETONÆMIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minimal model analysis of intravenous glucose tolerance test-derived insulin sensitivity in diabetic subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7988784

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00404339

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7988784%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7988784%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

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