• <em>POLG</em>-Related Disorders
• A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease
• Ataxias with autosomal, X-chromosomal or maternal inheritance
• Clinical and molecular features of POLG-related mitochondrial disease
• Comment on "Mobility spectrum computational analysis using a maximum entropy approach"
• Endoscope-Assisted Transmaxillosphenoidal Approach to the Sellar and Parasellar Regions: An Anatomic Study
• Epilepsy in mitochondrial disorders
• Inherited mitochondrial neuropathies
• Minocycline 1-year therapy in multiple-system-atrophy: effect on clinical symptoms and [(11)C] (R)-PK11195 PET (MEMSA-trial)
• Mitochondrial ataxias
• Mitochondrial disease and epilepsy
• Molecular and clinical genetics of mitochondrial diseases due to POLG mutations
• Pathogenicity in POLG syndromes: DNA polymerase gamma pathogenicity prediction server and database
• POLG-associated ataxias can represent a substantial part of recessive and sporadic ataxias in adults
• Predictors of medication adherence for African American patients diagnosed with hypertension
• Transport property of multi-band topological material PtBi[Formula: see text] studied by maximum entropy mobility spectrum analysis (MEMSA)