A5052700979- Mitochondrial Function and Pathology
- Metabolism and Genetic Disorders
- ATP Synthase and ATPases Research
- Ubiquitin and proteasome pathways
- Spine and Intervertebral Disc Pathology
- Adipose Tissue and Metabolism
- Eosinophilic Disorders and Syndromes
- Neurogenetic and Muscular Disorders Research
- Cardiac Imaging and Diagnostics
- Neurological diseases and metabolism
- Muscle Physiology and Disorders
- Sarcoma Diagnosis and Treatment
- Advanced MRI Techniques and Applications
- Tissue Engineering and Regenerative Medicine
Case Western Reserve University
2024
Louis Stokes Cleveland VA Medical Center
2024
St Vincent's Hospital
2004-2014
St. Vincent's Hospital
2004
DNA Diagnostic (Denmark)
2004
Many diverse pathogenic mitochondrial DNA (mtDNA) mutations have been described since 1988. The Melbourne Neuromuscular Research Institute (MNRI) has undertaken diagnostic detection of selected mtDNA 1990. MtDNA screened included point associated with Leber's hereditary optic neuropathy (LHON; G3460A, G11778A and T14484C), encephalopathy lactic acidosis stroke-like episodes (MELAS; A3243G), myoclonus epilepsy ragged red fibres (MERRF; A8344G) Leigh's syndrome/neuropathy ataxia retinitis...
Abstract Background and Purpose Spinal cord stimulation (SCS) is approved by the Food Drug Administration for treating chronic intractable pain in back, trunk, or limbs through of dorsal column. Numerous studies have used swine as an analog human spinal to better understand SCS further improve its efficacy. We performed high‐resolution imaging porcine with intact dura mater using micro‐computed tomography (μCT) construct detailed 3‐dimensional (3D) visualizations characterize morphology...