Disease: Sensory ataxic neuropathy- dysarthria- and ophthalmoparesis
- A case of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis with multiple mitochondrial DNA deletions
- A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease
- A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23
- Bilateral hypertrophic olivary degeneration in a syndrome of sensory ataxic neuropathy with dysarthria and ophthalmoplegia
- Bilateral Vestibulopathy Aggravates Balance and Gait Disturbances in Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis: A Case Report
- Clinical and Molecular Features of POLG-Related Sensory Ataxic Neuropathy with Dysarthria and Ophthalmoparesis
- Distinctive cerebral neuropathology in an adult case of sensory ataxic neuropathy with dysarthria and ophthalmoplegia (SANDO) syndrome
- Dopamine-agonist responsive Parkinsonism in a patient with the SANDO syndrome caused by POLG mutation
- Early-onset ataxia with progressive external ophthalmoplegia associated with POLG mutation: autosomal recessive mitochondrial ataxic syndrome or SANDO?
- MELAS/SANDO overlap syndrome associated with POLG1 mutations
- Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay
- Movement disorders in mitochondrial diseases
- MRI findings in SANDO variety of the ataxia-neuropathy spectrum with a novel mutation in POLG (c.3287G>T): A case report
- MRI findings in SANDO variety of the ataxia-neuropathy spectrum with a novel mutation in POLG (c.3287G>T): A case report
- Progressive external ophthalmoplegia
- Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation
- Protein molecular modeling shows residue T599 is critical to wild-type function of POLG and description of a novel variant associated with the SANDO phenotype
- Rod bipolar cell dysfunction in POLG retinopathy
- SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions
- Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism
- Sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO) in a sibling pair with a homozygous p.A467T POLG mutation
- Sensory ataxic neuropathy with dysarthria and ophthalmoparesis (SANDO) in late life due to compound heterozygous POLG mutations
- Sensory Ataxic Neuropathy with Dysarthria and Ophthalmoplegia (SANDO): A Multisystem Mitochondrial Disorder
- Sensory ataxic neuropathy with dysarthria/dysphagia and ophthalmoplegia (SANDO). Two case reports
- Sensory motor ataxic neuropathy associated dysarthria and ophthalmoplegia "SMANDO" in a consanguineous Moroccan patient with new POLG gene homozygote mutation
- The Y831C Mutation of the <em>POLG</em> Gene in Dementia
- What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?