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Publications by P. Maechler
Functional and Morphological Abnormalities of Mitochondria Harbouring the tRNA Leu(UUR) Mutation in Mitochondrial DNA Derived From Patients With Maternally Inherited Diabetes and Deafness (MIDD) and Progressive Kidney Disease
Diabetologia
Internal Medicine
Endocrinology
Metabolism
Diabetes
Peroxisome Proliferator-Activated Receptor Α (PPARα) Protects Against Oleate-Induced INS-1E Beta Cell Dysfunction by Preserving Carbohydrate Metabolism
Diabetologia
Internal Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Cystoid Macular Changes on Optical Coherence Tomography in a Patient With Maternally Inherited Diabetes and Deafness (MIDD)-associated Macular Dystrophy
Ophthalmic Genetics
Child Health
Ophthalmology
Pediatrics
Perinatology
Genetics
A Case of Diabetic Amyotrophy Associated With 3243 Mitochondrial tRNA(leu; UUR) Mutation and Successful Therapy With Coenzyme Q10.
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Maternally Inherited Deafness Associated With a T1095C Mutation in the mDNA
European Journal of Human Genetics
Genetics
Modifier Locus for Mitochondrial DNA Disease: Linkage and Linkage Disequilibrium Mapping of a Nuclear Modifier Gene for Maternally Inherited Deafness
Genetics in Medicine
Medicine
Genetics
Hypertrophic Cardiomyopathy in Patients With Diabetes Mellitus Associated With Mitochondrial tRNALeu(UUR) Gene Mutation.
Internal Medicine
Internal Medicine
Medicine
Mitochondrial Dysfunction in Inherited Renal Disease and Acute Kidney Injury
Nature Reviews Nephrology
Nephrology
Multiple Tumors in Mitochondrial Diabetes Associated With tRNALeu(UUR) Mutation at Position 3264
Diabetes Care
Internal Medicine
Endocrinology
Advanced
Metabolism
Specialized Nursing
Diabetes
Mitochondrial tRNALeu(UUR) Mutation at Position 3243 and Symptomatic Polyneuropathy in Type 2 Diabetes
Diabetes Care
Internal Medicine
Endocrinology
Advanced
Metabolism
Specialized Nursing
Diabetes
Prevalence of the Mitochondrial DNA A1555G Mutation in Sensorineural Deafness Patients in Island Southeast Asia
Journal of Human Genetics
Genetics