Browsing by Author North, Kathryn N

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Issue DateTitleAuthor(s)Citation
2015Expanding the phenotype of GMPPB mutationsClarke, Nigel; Corbett, Alastair; Ghaoui, Roula; Lek, Monkol; Reddel, Stephen; Sue, Carolyn; Waddell, Leigh Brook; Cabrera-Serrano, Macarena; Davis, Mark; Johnsen, Russell D; Kaur, Simranpreet; Laing, Nigel G; Lamont, Phillipa J.; Liang, Christina; MacArthur, Daniel; North, Kathryn N; Ravenscroft, Gianina; Childrens Hospital Westmead: Paediatrics & Child Health; Concord Clinical School: Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Concord Clinical School: ANZAC Research Institute; Northern Clinical School: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthExpanding the phenotype of GMPPB mutations, Brain, vol.138, Pt 4, 2015,pp 836-844
2010Factors Associated With Foot and Ankle Strength in Healthy Preschool-Age Children and Age-Matched Cases of Charcot-Marie-Tooth Disease Type 1ABurns, Joshua; Rose, Kristy; North, Kathryn N; Clinical and Rehabilitation Sciences; Children's Hospital Westmead: MedicineFactors Associated With Foot and Ankle Strength in Healthy Preschool-Age Children and Age-Matched Cases of Charcot-Marie-Tooth Disease Type 1A, Journal of Child Neurology, vol.25, 4,pp 463-468
2017The neural basis of deficient response inhibition in children with neurofibromatosis type 1: Evidence from a functional MRI studyKorgaonkar, Mayuresh; Barton, Belinda; North, Kathryn N; Payne, Johnathan; Pride, N; Westmead Clinical School: Westmead Institute for Medical ResThe neural basis of deficient response inhibition in children with neurofibromatosis type 1: Evidence from a functional MRI study, Cortex, vol.93, N/A, 2017,pp 1-11
2016Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related diseaseClarke, Nigel; Ghaoui, Roula; Lek, Monkol; Ma, Alan; Menezes, Manoj; O'Grady, Gina Louise; MacArthur, Daniel; Needham, Merrilee; North, Kathryn N; Peduto, Anthony J.; Sival, Deborah; van Ravenswaaij-Arts, Conny MA; Waddell, Leigh; Wong, Monica TY; Young, Helen; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Genetic Medicine; Clinical and Rehabilitation Sciences; Childrens Hospital Westmead: Paediatrics & Child HealthProminent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related disease, European Journal of Human Genetics, vol.24, 8, 2016,pp 1216-1219
2015Skeletal muscle and motor deficits in Neurofibromatosis Type 1Little, David; Payne, Jonathan; Quinlan (nee Edwards), Kate Gemma; Schindeler, Aaron; North, Kathryn N; Summers, M A; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthSkeletal muscle and motor deficits in Neurofibromatosis Type 1, Journal of Musculoskeletal and Neuronal Interactions, vol.15, 2, 2015,pp 161-170