Background: Progressive ataxia and palatal tremor (PAPT) can be observed in both acquired brainstem or cerebellar lesions and genetic disorders. Phenomenology shown: PAPT due to mutation in POLG, the gene encoding the mitochondrial DNA polymerase. Educational value: POLG mutation should be considered in patients with PAPT, particularly when additional clues such as a sensory neuronopathy or an ophthalmoplegia are present
OBJECTIVE: Mitochondrial dysfunction plays a key role in the pathophysiology of neurodegenerative di...
Objective: Polymerase gamma (POLG) mutations are a common cause of mitochondrial disease and have al...
Background: Mutations in the gene encoding the DNA-polymerase gamma (POLG), the enzyme that replicat...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
Progressive ataxia with palatal tremor (PAPT) is a syndrome caused by cerebellar and brainstem lesio...
Mitochondrial disease is phenotypically and genetically heterogeneous with an estimated prevalence o...
Even in the absence of classic features of mitochondrial disease, POLG1 should be considered in pati...
Different mutations, or combinations of mutations, in POLG1, the gene encoding pol γA, the catalytic...
International audienceObjective: Mitochondrial dysfunction plays a key role in the pathophysiology o...
Background Mitochondrial DNA maintenance disorders are an important cause of hereditary ataxia sy...
A 58-year-old woman presented with a 30-year history of progressive ataxia, dysarthria, and bilater...
Background: Cerebrotendinous xanthomatosis is a rare autosomal recessive neurometabolic disorder cha...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
BACKGROUND: Mutations in the mitochondrial DNA polymerase gamma are causing a wide phenotypic spectr...
Introduction: Polymerase γI (POLG) gene mutations may induce mitochondrial DNA (mtDNA) instability l...
OBJECTIVE: Mitochondrial dysfunction plays a key role in the pathophysiology of neurodegenerative di...
Objective: Polymerase gamma (POLG) mutations are a common cause of mitochondrial disease and have al...
Background: Mutations in the gene encoding the DNA-polymerase gamma (POLG), the enzyme that replicat...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
Progressive ataxia with palatal tremor (PAPT) is a syndrome caused by cerebellar and brainstem lesio...
Mitochondrial disease is phenotypically and genetically heterogeneous with an estimated prevalence o...
Even in the absence of classic features of mitochondrial disease, POLG1 should be considered in pati...
Different mutations, or combinations of mutations, in POLG1, the gene encoding pol γA, the catalytic...
International audienceObjective: Mitochondrial dysfunction plays a key role in the pathophysiology o...
Background Mitochondrial DNA maintenance disorders are an important cause of hereditary ataxia sy...
A 58-year-old woman presented with a 30-year history of progressive ataxia, dysarthria, and bilater...
Background: Cerebrotendinous xanthomatosis is a rare autosomal recessive neurometabolic disorder cha...
Background: The pathophysiology of the movement disorder progressive ataxia with palatal tremor (PAP...
BACKGROUND: Mutations in the mitochondrial DNA polymerase gamma are causing a wide phenotypic spectr...
Introduction: Polymerase γI (POLG) gene mutations may induce mitochondrial DNA (mtDNA) instability l...
OBJECTIVE: Mitochondrial dysfunction plays a key role in the pathophysiology of neurodegenerative di...
Objective: Polymerase gamma (POLG) mutations are a common cause of mitochondrial disease and have al...
Background: Mutations in the gene encoding the DNA-polymerase gamma (POLG), the enzyme that replicat...