Sébastien Lebon
University Hospital of Lausanne
26 papers found
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Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome
UploadAutosomal recessive primary microcephaly due to ASPM mutations: An update
Download from api.wiley.comDefining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities
Download from archpsyc.jamanetwork.comWhen should clinicians search for GLUT1 deficiency syndrome in childhood generalized epilepsies?
UploadThe wide spectrum of tubulinopathies: What are the key features for the diagnosis?
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