International audienceBackground. - While it is known that 22q11.2 microdeletions (22q11.2-del) increase the risk of Parkinson's disease (PD), the characteristics of PD associated with 22q11.2-del have not been specifically explored.Objective. - This report aimed to assess the clinical characteristics and treatment responses of PD patients with 22q11.2-del, and to describe any features that might lead neurologists to investigate the comorbidity.Methods. - Nine PD patients (eight men, one woman) with 22q11.2-del were followed at seven centers of the French PD Expert Network (Ns-Park). Results. - PD diagnosis was made before 22q11.2-del diagnosis in seven cases; their main characteristics were early onset (32-48 years) and good initial levodo...
The 22q11 deletion syndrome (22q11DS) is one of the most common genomic disorders in humans. There i...
To investigate disease risk mechanisms of early-onset Parkinson's disease (PD) associated with the r...
Background: 22q11.2 deletion syndrome (22q11.2DS) is considered as the genetic model of schizophreni...
International audienceBackground. - While it is known that 22q11.2 microdeletions (22q11.2-del) incr...
OBJECTIVE: To delineate the natural history, diagnosis, and treatment response of Parkinson disease ...
Background: 22q11.2 deletion syndrome (22q11.2DS) is a multisystem condition associated with an incr...
The etiology of Parkinson’s disease (PD) remains largely unknown with the exception of a few genetic...
Background: The recurrent hemizygous 22q11.2 deletion associated with 22q11.2 deletion syndrome has ...
Background Parkinson's disease has been reported in a small number of patients with chromosome 22q11...
22q11.2 microdeletions are among the most common deletions found in humans. Whereas most cases prese...
The 22q11 deletion syndrome (22q11DS) is one of the most common genomic disorders in humans. There i...
To investigate disease risk mechanisms of early-onset Parkinson's disease (PD) associated with the r...
Background: 22q11.2 deletion syndrome (22q11.2DS) is considered as the genetic model of schizophreni...
International audienceBackground. - While it is known that 22q11.2 microdeletions (22q11.2-del) incr...
OBJECTIVE: To delineate the natural history, diagnosis, and treatment response of Parkinson disease ...
Background: 22q11.2 deletion syndrome (22q11.2DS) is a multisystem condition associated with an incr...
The etiology of Parkinson’s disease (PD) remains largely unknown with the exception of a few genetic...
Background: The recurrent hemizygous 22q11.2 deletion associated with 22q11.2 deletion syndrome has ...
Background Parkinson's disease has been reported in a small number of patients with chromosome 22q11...
22q11.2 microdeletions are among the most common deletions found in humans. Whereas most cases prese...
The 22q11 deletion syndrome (22q11DS) is one of the most common genomic disorders in humans. There i...
To investigate disease risk mechanisms of early-onset Parkinson's disease (PD) associated with the r...
Background: 22q11.2 deletion syndrome (22q11.2DS) is considered as the genetic model of schizophreni...