Perry syndrome is a rare, adult-onset, autosomal dominant, progressive neurodegenerative disorder that is characterized by parkinsonism, weight loss, psychiatric symptoms, and central hypoventilation. We report the case of a 51-year-old man, whose condition was genetically identified as Perry syndrome. Here we focus the polysomnographic (PSG) findings and discuss the correlations between PSG and neuropathological findings
peer reviewedBACKGROUND: Sleep abnormalities in Parkinson's disease (PD) are frequent, but it is unk...
The 22q11 deletion syndrome (22q11DS) is one of the most common genomic disorders in humans. There i...
Wilson's disease (WD) has neuro-anatomical, pathophysiological and neurochemical basis for sleep dis...
Background: Sleep disturbances are common non-motor symptoms of Parkinson's Disease (PD). Methods...
BACKGROUND: Perry syndrome (PS) caused by DCTN1 gene mutation is clinically characterized by autosom...
Parkinson’s disease (PD) is the second most common neurodegenerative disease in the world, and aging...
Objective: To determine the pathologic substrates in patients with rapid eye movement (REM) sleep be...
Scientific BACKGROUND: Wilson’s disease (WD) is an autosomal recessive degenerative disorder of co...
Méthode : Nous avons réalisé une étude rétrospective de polysonographies (PSG) et de dossiers médica...
Introduction. Progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS) are clinical mani...
Introduction: Parkinson’s Disease (PD), a common neurodegenerative disease worldwide, has few reliab...
Background:Phospholipase-associated neurodegeneration (PLAN) caused by PLA2G6 mutations is a recessi...
peer reviewedBackground: Polysomnography (PSG) data are rare in patients who have early stage idiopa...
Objective Sleep disorders in Parkinson’s disease are very common. Polysomnography (PSG) is considere...
Sleep dysfunction is recognized as a distinct clinical manifestation in movement disorders, often re...
peer reviewedBACKGROUND: Sleep abnormalities in Parkinson's disease (PD) are frequent, but it is unk...
The 22q11 deletion syndrome (22q11DS) is one of the most common genomic disorders in humans. There i...
Wilson's disease (WD) has neuro-anatomical, pathophysiological and neurochemical basis for sleep dis...
Background: Sleep disturbances are common non-motor symptoms of Parkinson's Disease (PD). Methods...
BACKGROUND: Perry syndrome (PS) caused by DCTN1 gene mutation is clinically characterized by autosom...
Parkinson’s disease (PD) is the second most common neurodegenerative disease in the world, and aging...
Objective: To determine the pathologic substrates in patients with rapid eye movement (REM) sleep be...
Scientific BACKGROUND: Wilson’s disease (WD) is an autosomal recessive degenerative disorder of co...
Méthode : Nous avons réalisé une étude rétrospective de polysonographies (PSG) et de dossiers médica...
Introduction. Progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS) are clinical mani...
Introduction: Parkinson’s Disease (PD), a common neurodegenerative disease worldwide, has few reliab...
Background:Phospholipase-associated neurodegeneration (PLAN) caused by PLA2G6 mutations is a recessi...
peer reviewedBackground: Polysomnography (PSG) data are rare in patients who have early stage idiopa...
Objective Sleep disorders in Parkinson’s disease are very common. Polysomnography (PSG) is considere...
Sleep dysfunction is recognized as a distinct clinical manifestation in movement disorders, often re...
peer reviewedBACKGROUND: Sleep abnormalities in Parkinson's disease (PD) are frequent, but it is unk...
The 22q11 deletion syndrome (22q11DS) is one of the most common genomic disorders in humans. There i...
Wilson's disease (WD) has neuro-anatomical, pathophysiological and neurochemical basis for sleep dis...