Browsing by Author Scherer, Steven

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Issue DateTitleAuthor(s)Citation
2015CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysisBurns, Joshua; Bacon, C; Bundy, B; Day, J; Feely, S.; Finkel, R S; Fridman, Vera; Grider, T; Herrmann, David; Kirk, C A; Laura, Matilde; Li, J; Lloyd, Thomas; Moroni, I; Muntoni, Francesco; Pagliano, E; Pareyson, Davide; Piscosquito, G; Ramchandren, S; Reilly, M; Scherer, Steven; Shy, Michael; Shy, Rosemary; Siskind, C; Sumner, Charlotte; Yum, Sabrina; Zuchner, Stephan; Clinical and Rehabilitation SciencesCMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis, Journal of Neurology, Neurosurgery and Psychiatry, vol.86, 8, 2015,pp 873-878
2015Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ geneBurns, Joshua; Bacon, C; Day, J; Feely, SME; Finkel, R S; Grider, T; Herrmann, David; Laura, Matilde; Li, J; Lloyd, Thomas; Moroni, Isabella; Muntoni, Francesco; Pareyson, Davide; Piscosquito, G; Ramchandren, Sindhu; Reilly, Mary; Sanmaneechai, Oranee; Scherer, Steven; Shy, Michael; Shy, Rosemary; Siskind, C; Sumner, Charlotte; Yum, Sabrina; Clinical and Rehabilitation SciencesGenotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene, Brain, vol.138, 11, 2015,pp 3180-3192
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