Cathy E. Woodward

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology

Claudia B. Catarino, Joan Liu, Ioannis Liagkouras et al. · Brain · 2011 · 227 citations · Full text

Medicine, Neurology, Neuroscience +17

Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I)

Henry Houlden, R. H. M. King, Julian Blake et al. · Brain · 2005 · 140 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Paediatric single mitochondrial DNA deletion disorders: an overlapping spectrum of disease

Alexander Broomfield, Mary G. Sweeney, Cathy E. Woodward et al. · Journal of Inherited Metabolic Disease · 2014 · 136 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

NDUFA4 Mutations Underlie Dysfunction of a Cytochrome c Oxidase Subunit Linked to Human Neurological Disease

Robert D. S. Pitceathly, Shamima Rahman, Yehani Wedatilake et al. · Cell Reports · 2013 · 128 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genetic dysfunction of <i>MT-ATP6</i> causes axonal Charcot-Marie-Tooth disease

Robert D. S. Pitceathly, Sinéad M. Murphy, Ellen Cottenie et al. · Neurology · 2012 · 111 citations · Full text

Life Sciences, Genetics, Neurology +17