none8siObjective: To characterise the distinctive eye movement disorder and the sleep-related dyskinesia in Adenylate cyclase 5 (ADCY5) related disease. Methods: Formal eye movement examination and video-polysomnography in a cohort of patients with ADCY5 mutations. Results: All three patients had an eye movement disorder characterised by oculomotor apraxia with gaze limitation most prominently in the vertical plane. All patients had disrupted sleep architecture with reduced sleep efficiency due to frequent and prolonged arousals and awakenings in the context of dyskinesia, which could arise from any sleep stage. The nocturnal movements could last up to 30 min and be more severe than those seen during day-time. Conclusion: Nocturnal exacerba...
Congenital ocular motor apraxia (COMA) is a unique ocular motor disorder which is characterized by a...
Objective: Anti-IgLON5 disease is a recently described neurological disease that shares features of ...
Objective: To outline specific sleep disturbances in different clinical subsets of Attention Deficit...
Objective: To characterise the distinctive eye movement disorder and the sleep-related dyskinesia in...
BackgroundAdenylyl cyclase 5 (ADCY5)-related movement disorder (ADCY5-RMD) is a rare, childhood-onse...
Background Adenylyl cyclase 5 (ADCY5)-related movement disorder (ADCY5-RMD) is a rare, childhood-ons...
Background:The phenotypic spectrum of adenylyl cyclase 5 (ADCY5)-related disease has expanded consid...
Background The phenotypic spectrum of adenylyl cyclase 5 (ADCY5)‐related disease has expanded consi...
BACKGROUND: Adenylyl cyclase 5 (ADCY5) mutations is associated with heterogenous syndromes: familial...
Adenylyl cyclase 5 (ADCY5)-related phenotypes comprise an expanding disease continuum, but much rema...
Mutations in the ADCY5 gene can cause a complex hyperkinetic movement disorder. Episodic exacerbatio...
<p>The phenotypic and genetic spectrum of ataxia with oculomotor apraxia (AOA) disorders is rapidly ...
Failure to Initiate Voluntary Horizontal Saccadic Eye Movements; Head thrustPowerPoint Presentation:...
Congenitaloculomotor apraxia (AOA) is a disease caused by the autosomal recessive SETX mutation. A 2...
Narcolepsy with cataplexy is characterized by daytime sleepiness, cataplexy (sudden loss of bilatera...
Congenital ocular motor apraxia (COMA) is a unique ocular motor disorder which is characterized by a...
Objective: Anti-IgLON5 disease is a recently described neurological disease that shares features of ...
Objective: To outline specific sleep disturbances in different clinical subsets of Attention Deficit...
Objective: To characterise the distinctive eye movement disorder and the sleep-related dyskinesia in...
BackgroundAdenylyl cyclase 5 (ADCY5)-related movement disorder (ADCY5-RMD) is a rare, childhood-onse...
Background Adenylyl cyclase 5 (ADCY5)-related movement disorder (ADCY5-RMD) is a rare, childhood-ons...
Background:The phenotypic spectrum of adenylyl cyclase 5 (ADCY5)-related disease has expanded consid...
Background The phenotypic spectrum of adenylyl cyclase 5 (ADCY5)‐related disease has expanded consi...
BACKGROUND: Adenylyl cyclase 5 (ADCY5) mutations is associated with heterogenous syndromes: familial...
Adenylyl cyclase 5 (ADCY5)-related phenotypes comprise an expanding disease continuum, but much rema...
Mutations in the ADCY5 gene can cause a complex hyperkinetic movement disorder. Episodic exacerbatio...
<p>The phenotypic and genetic spectrum of ataxia with oculomotor apraxia (AOA) disorders is rapidly ...
Failure to Initiate Voluntary Horizontal Saccadic Eye Movements; Head thrustPowerPoint Presentation:...
Congenitaloculomotor apraxia (AOA) is a disease caused by the autosomal recessive SETX mutation. A 2...
Narcolepsy with cataplexy is characterized by daytime sleepiness, cataplexy (sudden loss of bilatera...
Congenital ocular motor apraxia (COMA) is a unique ocular motor disorder which is characterized by a...
Objective: Anti-IgLON5 disease is a recently described neurological disease that shares features of ...
Objective: To outline specific sleep disturbances in different clinical subsets of Attention Deficit...