Mitochondrial diabetes: Pathophysiology, clinical presentation, and genetic analysis
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference32 articles.
1. Importance of maternal history of non-insulin dependent diabetic patients.
2. New windows on the mechanism of action of KATP channel openers
3. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion
4. Renal Failure from Mitochondrial Cytopathies
5. The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency and Concomitant Reduced Association of mRNA with Ribosomes
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4. Delayed diagnoses of mitochondrial cytopathies in patients presenting with end stage kidney disease: two case reports;BMC Nephrology;2020-08-24
5. Diabetes Type 4: A Paradigm Shift in the Understanding of Glaucoma, the Brain Specific Diabetes and the Candidature of Insulin as a Therapeutic Agent;Current Molecular Medicine;2017-04-10
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