Browsing by Author Meyer, Esther

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Issue DateTitleAuthor(s)Citation
2015The clinical and genetic heterogeneity of paroxysmal dyskinesiasDale, Russell; Erro, Roberto; et al, Various; Gardiner, Alice; Jaffer, Fatima; Kullmann, Dimitri; Labrum, Robyn; Meyer, Esther; Stamelou, Maria; Walker, Matthew; Warner, Tom; Xiromerisiou, Georgia; Childrens Hospital Westmead: Paediatrics & Child HealthThe clinical and genetic heterogeneity of paroxysmal dyskinesias, Brain, vol.138, Pt 12, 2015,pp 3567-3580
2016Delineation of the movement disorders associated with FOXG1 mutationsMohammad, Shekeeb; Augustine, Erika; et al, Various; Hemingway, Cheryl; Mankad, Kshitij; McTague, Amy; Meyer, Esther; Ng, Joanne; Ngoh, Adeline; Papandreou, Apostolos; Schneider, Ruth; Children's Hospital Westmead: Childrens Medical Research InsDelineation of the movement disorders associated with FOXG1 mutations, Neurology, vol.86, 19, 2016,pp 1794-1800
2016Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystoniaDale, Russell; Mohammad, Shekeeb; Abdul-Sada, Alaa; Chong, W Kling; Dadswell, Chris; et al, Various; Hung, Christina Y.; Meyer, Esther; Simpson, Michael A.; Tuschl, Karin; Valdivia, Leonardo E.; Zhao, Ningning; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research InsMutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia, Nature Communications, vol.7, N/A, 2016,pp 1-16
2017Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaDale, Russell; Misra, S; Mohammad, Shekeeb; Peters, Gregory; Carss, Keren; et al, Various; Grozeva, Detelina; Joseph, Agnel; Mencacci, Niccolo; Meyer, Esther; Ng, Joanne; Nichols, John; Papandreou, Apostolos; Rankin, Julia; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Childrens Hospital Westmead: Paediatrics & Child HealthMutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia, Nature Genetics, vol.49, 2, 2017,pp 223-237