Literature DB >> 7589871

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.

M Odawara, K Tada, K Yamashita.   

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Year:  1995        PMID： 7589871     DOI： 10.1007/BF00400594

Source DB:  PubMed          Journal:  Diabetologia        ISSN： 0012-186X            Impact factor:   10.122


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  5 in total

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

Authors:  Y Goto; I Nonaka; S Horai
Journal:  Nature       Date:  1990-12-13       Impact factor: 49.962

2.  Repair of oxidative damage within the mitochondrial DNA of RINr 38 cells.

Authors:  W J Driggers; S P LeDoux; G L Wilson
Journal:  J Biol Chem       Date:  1993-10-15       Impact factor: 5.157

3.  Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene.

Authors:  M Odawara; K Sasaki; K Yamashita
Journal:  J Clin Endocrinol Metab       Date:  1995-04       Impact factor: 5.958

4.  Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.

Authors:  J M van den Ouweland; H H Lemkes; W Ruitenbeek; L A Sandkuijl; M F de Vijlder; P A Struyvenberg; J J van de Kamp; J A Maassen
Journal:  Nat Genet       Date:  1992-08       Impact factor: 38.330

Review 5.  Cerebral function in diabetes mellitus.

Authors:  G J Biessels; A C Kappelle; B Bravenboer; D W Erkelens; W H Gispen
Journal:  Diabetologia       Date:  1994-07       Impact factor: 10.122
  5 in total

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