Browsing by Author Antony, Jayne

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Issue DateTitleAuthor(s)Citation
2012Accelerated long-term forgetting in children with idiopathic generalized epilepsyBarton, Belinda; Gascoigne, Michael; Lah, Suncica; Antony, Jayne; Gill, Deepak S; Webster, Richard; Children's Hospital Westmead: Paediatrics & Child Health; Psychology; PsychologyAccelerated long-term forgetting in children with idiopathic generalized epilepsy, Epilepsia, vol.53, 12, 2012,pp 2135-2140
2003Acute flaccid paralysis in Australian childrenElliott, Elizabeth; Morris, Anne; Antony, Jayne; D'Souza, R. M.; Kennett, M.; Longbottom, H.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthAcute flaccid paralysis in Australian children, Journal of Paediatrics and Child Health, vol.39,(1),2003,pp 22-26
2016Auditory neuropathy in Brown-Vialetto-Van Laere syndrome dueto riboflavin transporter RFVT2 deficiencyMenezes, Manoj; Ouvrier, Robert; Antony, Jayne; Birman, Catherine; Gardner-Berry, Kirsty; Hill, Mandy; O'Brien, Katherine; Webster, Richard; Clinical and Rehabilitation Sciences; Childrens Hospital Westmead: Paediatrics & Child HealthAuditory neuropathy in Brown-Vialetto-Van Laere syndrome dueto riboflavin transporter RFVT2 deficiency, Developmental Medicine and Child Neurology, vol.58, 8, 2016,pp 848-854
2012Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraineDale, Russell; Antony, Jayne; Gardiner, Alice; Houlden, Henry; Children's Hospital Westmead: Paediatrics & Child HealthFamilial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine, Developmental Medicine and Child Neurology, vol.54, 10, 2012,pp 958-960
2016Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporterBurns, Joshua; Kiernan, Matthew; Menezes, Manoj; Ouvrier, Robert; Vucic, Steve; Antony, Jayne; Farrar, Michelle; O'Brien, Katie; Webster, Richard; Clinical and Rehabilitation Sciences; Central Clinical School: Medicine; Clinical and Rehabilitation Sciences; Childrens Hospital Westmead: Paediatrics & Child Health; Western Clinical School: Medicine (Westmead)Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporter, Clinical Neurophysiology, vol.127, 1, 2016,pp 911-918
2003Peripheral neuropathies of infancyNicholson, Garth; Pollard, John; Antony, Jayne; Ouvrier, Robert; Wilmhurst, Jo M.; Concord Clinical School: ANZAC Research Institute; Central Clinical School: MedicinePeripheral neuropathies of infancy, Developmental Medicine and Child Neurology, vol.45,(6),2003,pp 408-414
2014Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2Al-Odaib, Ahmad; Burns, Joshua; Carpenter, Kevin; Christodoulou, John; Gold, Wendy; Lek, Monkol; Menezes, Manoj; Ouvrier, Robert; Wang, Min-Xia; Zuchner, Stephen; Abrams, Alexander; Antony, Jayne; Baxter, Peter; Brandner, Sebastian; Broomfield, Alexander; Clayton, P.; Farrell, Michael; Foley, A Reghan; Forman, Eva; Gonzalez, Michael; Hargreaves, Iain; Horvath, Rita; Houlden, Henry; Hughes, Imelda; Jungbluth, Heinz; King, Mary D.; Land, John; Lim, Ming; Lin, Jean-Pierre; Manzur, Adnan; Mathew, Ann; Matsubara, Kazuo; McCullagh, B. Gary; McGarvey, Michael; Megarbane, Andre; Muntoni, Francesco; Ng, Joanne; O’Byrne, James; O'Brien, Katherine; Olpin, Simon; Oppenheim, Marcus; Pandraud, Amelie; Phadke, Rahul; Prasad, Manish; Rahman, Shamima; Reilly, Mary; Scherer, Steven; Scoto, Mariacristina; Shah, Ayaz; Straub, Volker; Sugano, Kumiko; Urtizberea, Jon Andoni; Webster, Richard; Yonezawa, Atsushi; Childrens Hospital Westmead: Paediatrics & Child Health; Clinical and Rehabilitation Sciences; Children's Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Clinical and Rehabilitation Sciences; Childrens Hospital Westmead: Paediatrics & Child Health; Central Clinical School: MedicineTreatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2, Brain, vol.137, Pt 1, 2014,pp 44-56
2011VGKC antibodies in pediatric encephalitis presenting with status epilepticusBrilot-Turville, Fabienne; Dale, Russell; Suleiman, Jehan; Antony, Jayne; Brenner, T.; Gill, D; Lang, B; Vincent, A; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthVGKC antibodies in pediatric encephalitis presenting with status epilepticus, Neurology, vol.76, 14, 2011,pp 1252-1255