Browsing by Author Schneider, Susanne

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Issue DateTitleAuthor(s)Citation
2012PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraineDale, Russell; Bhatia, Kailash P; Counihan, Tim; et al, Various; Gardiner, Alice; Kurian, Manju; Schapira, Anthony H V; Schneider, Susanne; Spacey, Sian D.; Stamelou, Maria; Valente, Enza-Maria; Wali, G; Children's Hospital Westmead: Paediatrics & Child HealthPRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine, Neurology, vol.79, 21, 2012,pp 2115-2121