Browsing by Author Menezes, Manoj

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Issue DateTitleAuthor(s)Citation
2014Randomised controlled trial protocol of foot and ankle exercise for children with Charcot-Marie-Tooth diseaseBurns, Joshua; Menezes, Manoj; Ouvrier, Robert; Raymond, Jacqueline; Refshauge, Kathryn; Sman, Amy; Walker, Terri; Clinical and Rehabilitation Sciences; Clinical and Rehabilitation Sciences; Childrens Hospital Westmead: Paediatrics & Child Health; Exercise Health and Performance; Clinical and Rehabilitation Sciences; Clinical and Rehabilitation SciencesRandomised controlled trial protocol of foot and ankle exercise for children with Charcot-Marie-Tooth disease, Journal of Physiotherapy, vol.60, 1, 2014,pp 55-55
2013Rapidly progressive asymmetrical weakness in Charcot-Marie-Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathyMenezes, Manoj; Anderson, Janice; Blake, Julian; Brandner, Sebastian; Cottenie, Ellen; Dick, David; Houlden, Henry; Jaunmuktane, Zane; Morrow, Jasper; Reilly, M; Rossor, Alexander; Yousry, Tarek; Children's Hospital Westmead: Paediatrics & Child HealthRapidly progressive asymmetrical weakness in Charcot-Marie-Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathy, Neuromuscular Disorders, vol.23, 5, 2013,pp 399-403
2017Safety and efficacy of progressive resistance exercise for Charcot-Marie-Tooth disease in children: a randomised, double-blind, sham-controlled trialBurns, Joshua; Cornett, Kayla; Mandarakas, Melissa; Menezes, Manoj; Raymond, Jacqueline; Refshauge, Kathryn; Rose, Kristy Joy; Sman, Amy; Wojciechowski, Elizabeth; Bray, Paula; Farrar, Michelle; Sampaio, Hugo; Walker, Terri; Clinical and Rehabilitation Sciences; Physiotherapy; Clinical and Rehabilitation Sciences; Clinical and Rehabilitation Sciences; Exercise Health and Performance; Clinical and Rehabilitation Sciences; Clinical and Rehabilitation Sciences; Clinical and Rehabilitation Sciences; Health SciencesSafety and efficacy of progressive resistance exercise for Charcot-Marie-Tooth disease in children: a randomised, double-blind, sham-controlled trial, The Lancet Child & Adolescent Health, vol.1, 2, 2017,pp 106-113
2015Systematic review of exercise for Charcot-Marie-Tooth diseaseBurns, Joshua; Fiatarone Singh, Maria Antoinette; Fornusek, Che; Hackett, Daniel; Sman, Amy; Menezes, Manoj; Clinical and Rehabilitation Sciences; Exercise Health and Performance; Exercise Health and Performance; Exercise Health and Performance; Clinical and Rehabilitation SciencesSystematic review of exercise for Charcot-Marie-Tooth disease, Journal of the Peripheral Nervous System, vol.20, 4, 2015,pp 347-362
2013Transitioning outcome measures: relationship between the CMTPedS and CMTNSv2 in children, adolescents, and young adults with Charcot-Marie-Tooth diseaseBurns, Joshua; Menezes, Manoj; Eichinger, Kate; Estilow, Tim; Finkel, Richard; Herrmann, David; Laura, Matilde; Moroni, Isabella; Muntoni, Francesco; Pagliano, Emanuela; Pareyson, Davide; Reilly, Mary; Shy, Michael; Shy, Rosemary R; Clinical and Rehabilitation Sciences; Children's Hospital Westmead: Paediatrics & Child HealthTransitioning outcome measures: relationship between the CMTPedS and CMTNSv2 in children, adolescents, and young adults with Charcot-Marie-Tooth disease, Journal of the Peripheral Nervous System, vol.18, 2, 2013,pp 177-180
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
2016Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndromeBest, Heather; Clarke, Nigel; Cooper, Sandra; Menezes, Manoj; North, Kathryn; O'Grady, Gina Louise; Benavides Damm, Tatiana; Engel, Andrew; Fock, Johanna; Kamsteeg, Erik-Jan; Lek, Monkol; MacArthur, Daniel; Pride, Natalie; Turner, Christian; Verschuuren, Corien; Webster, Richard; Yuen, Michaela; 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; Childrens Hospital Westmead: Paediatrics & Child HealthVariants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome, Neurology, vol.87, 14, 2016,pp 1442-1448
2014Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth diseaseClarke, Nigel; Menezes, Manoj; Waddell, Leigh Brook; Kaur, Simranpreet; Lenk, Guy; MacArthur, Daniel; Meisler, Miriam H.; Childrens Hospital Westmead: Paediatrics & Child Health; Clinical and Rehabilitation Sciences; Childrens Hospital Westmead: Paediatrics & Child HealthWhole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth disease, Neuromuscular Disorders, vol.24, 8, 2014,pp 666-670
2016Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3Brewer, Megan Hwa; Chaudhry, Rabia; Kennerson, Marina; Menezes, Manoj; Nicholson, Garth; Qi, Jessica; Young, Helen Kathryn; Drew, Alexander P; Farrar, Michelle A; Kidambi, Aditi; Mowat, David; Reddel, Stephen; Ryan, Monique; Subramanian, Gopinath M; Zuchner, Stephan; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research Institute; Clinical and Rehabilitation Sciences; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: Pathology; Childrens Hospital Westmead: Paediatrics & Child HealthWhole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3, PLoS Genetics, vol.12, 7, 2016,pp Article number e1006177-N/A