The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
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Treatment for mitochondrial disordersMonogenic diabetes and pregnancyCoenzyme Q10 protects hair cells against aminoglycosideMitochondrial dysfunction in diabetes: from molecular mechanisms to functional significance and therapeutic opportunities.Pearls & oy-sters: maternally inherited diabetes and deafness presenting with ptosis and macular pattern dystrophy.Targeting cellular energy production in neurological disorders.A family with diabetes and heart failure.Maternal transmission of diabetes.Mitochondrial diabetes mellitus.Current experience in testing mitochondrial nutrients in disorders featuring oxidative stress and mitochondrial dysfunction: rational design of chemoprevention trials.Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis.Effects of CoQ10 Supplementation on Lipid Profiles and Glycemic Control in Patients with Type 2 Diabetes: a randomized, double blind, placebo-controlled trial.Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.New treatments for mitochondrial disease-no time to drop our standards.Monogenic diabetes: a diagnostic algorithm for cliniciansIs there a place for coenzyme Q in the management of metabolic disorders associated with obesity?Low prevalence of patients with mitochondrial disease in the German/Austrian DPV diabetes registry.Diabetes and nephrotic syndrome: Answers.Overnight inhibition of insulin secretion restores pulsatility and proinsulin/insulin ratio in type 2 diabetes.Insight into age-related macular degeneration: new vision in sight.Alterations of rCBF and mitochondrial dysfunction in major depressive disorder: a case report.Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism.Coenzyme Q-10 treatment of patients with a 7445A--->G mitochondrial DNA mutation stops the progression of hearing loss.Etiologic diagnosis of sensorineural hearing loss in adults.Coenzyme Q10 suppresses apoptosis of mouse pancreatic β-cell line MIN6.Monogenic Causes of Diabetes
P2860
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P2860
The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh-hant
name
The effects of coenzyme Q10 tr ...... al DNA 3243 (A to G) mutation.
@en
The effects of coenzyme Q10 tr ...... al DNA 3243 (A to G) mutation.
@nl
type
label
The effects of coenzyme Q10 tr ...... al DNA 3243 (A to G) mutation.
@en
The effects of coenzyme Q10 tr ...... al DNA 3243 (A to G) mutation.
@nl
prefLabel
The effects of coenzyme Q10 tr ...... al DNA 3243 (A to G) mutation.
@en
The effects of coenzyme Q10 tr ...... al DNA 3243 (A to G) mutation.
@nl
P2093
P356
P1433
P1476
The effects of coenzyme Q10 tr ...... al DNA 3243 (A to G) mutation.
@en
P2093
P2888
P304
P356
10.1007/S001250050950
P577
1998-05-01T00:00:00Z