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- 2017
-
Mark
Respiratory chain complex III deficiency due to mutated BCS1L : A novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
- Contribution to journal › Article
-
Mark
Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss : A whole mitochondrial genome screening
- Contribution to journal › Article
-
Mark
Mitochondrial dysfunction and metabolic intervention
(2017)
- Thesis › Doctoral thesis (compilation)
-
Mark
Cerebral Mitochondrial Dysfunction and the Development of Targeted Therapeutics
(2017)
- Thesis › Doctoral thesis (compilation)
-
Mark
Hospitalizations for mitochondrial disease across the lifespan in the U.S
- Contribution to journal › Article
-
Mark
Oxygen consumption in platelets as an adjunct diagnostic method for pediatric mitochondrial disease
- Contribution to journal › Article
- 2016
-
Mark
Diverse and Tissue Specific Mitochondrial Respiratory Response in A Mouse Model of Sepsis-Induced Multiple Organ Failure.
- Contribution to journal › Article
-
Mark
Changes in energy metabolism due to acute rotenone-induced mitochondrial complex I dysfunction – An in vivo large animal model
- Contribution to journal › Article
-
Mark
Mitochondrial Respiratory Function in Peripheral Blood Cells from Huntington's Disease Patients
- Contribution to journal › Article
-
Mark
White adipose tissue browning in the R6/2 mouse model of Huntington's disease
- Contribution to journal › Article
