| Unbound MEDLINE results for: | Bookmark this site | | Articles related to 18826862 [Unique ID], provided by the PubMed system | |
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| | 1 - 10 of 102 journal articles in the PubMed database | Email to a friend | | |
| Shimizu1 J, 2 , Inatsu1 A, et al.
Hyperkalemia in familial mitochondrial cytopathy. [JOURNAL ARTICLE]
Clin Nephrol 2008 Oct; Volume 70(October):348-353.
Abstract | Full Citation | Find Related Articles | | Hotta O, Inoue CN, Miyabayashi S, et al.
Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation. [Journal Article]
Kidney Int 2001 Apr; 59(4):1236-43.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Dinour D, Mini S, Polak-Charcon S, et al.
Progressive nephropathy associated with mitochondrial tRNA gene mutation. [Case Reports, Journal Article]
Clin Nephrol 2004 Aug; 62(2):149-54.
Abstract | Full Citation | Find Related Articles | | Hsieh RH, Li JY, Pang CY, et al.
A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy. [Case Reports, Journal Article]
J Biomed Sci 2001 Jul-Aug; 8(4):328-35.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Liou CW, Huang CC, Wei YH
Molecular analysis of diabetes mellitus-associated A3243G mitochondrial DNA mutation in Taiwanese cases. [Journal Article]
Diabetes Res Clin Pract 2001 Dec.:S39-43.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Harrison TJ, Boles RG, Johnson DR, et al.
Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy. [Case Reports, Journal Article]
Am J Ophthalmol 1997 Aug; 124(2):217-21.
Abstract | Full Citation | Find Related Articles | | Morovvati S, Nakagawa M, Sato Y, et al.
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation. [Journal Article]
Acta Neurol Scand 2002 Aug; 106(2):104-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kobayashi T, Nakanishi K, Nakase H, et al.
In situ characterization of islets in diabetes with a mitochondrial DNA mutation at nucleotide position 3243. [Case Reports, Journal Article]
Diabetes 1997 Oct; 46(10):1567-71.
Abstract | Full Citation | Find Related Articles | | Stratilová L, Zeman J, Hansíková H, et al.
[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA] [Case Reports, Journal Article]
Cas Lek Cesk 1998 Jul 13; 137(14):430-3.
Abstract | Full Citation | Find Related Articles |   |
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