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Ohlenbusch, A.
Acute and Episodic Movement Disorders: ATP1A3-Related Disorders as Differential Diagnosis
Omram, H.
Ciliogenesis Defect of Multiple Motile Cilia Causes Hydrocephalus
Omran, H.
Ciliopathies and Defects of Brain Development
The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System
Ong, T.
Meta-analyses of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy
Lung Function in Ataluren-Treated, Nonambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy from a Long-Term Extension Trial
Opp, J.
Advantages of Starting Methylphenidate in a Double-Blind Trial
X-ALD as the Cause of Autistic Behavior
Ortigoza-Escobar, J. D.
Successfully Completed Pregnancy in a Patient with SLC25A19-Associated Form of a Treatable Leigh-Like Syndrome
Osinski, D.
BNS Epilepsy, Global Developmental Delay, Optic Coloboma, and Vesicoureteral Reflux as Leading Symptoms of COL4A1 Mutation: A Case Report
Oster, I.
Acute Flaccid Myelitis (AFM) Associated with Enterovirus: A Distinct Clinical Entity?
Otten, K.
Severe Cortical Malformation and Acquired Cataract: An Unusual Presentation of DYNC1H1 Mutation in Twins