Browsing by Author Rossor, Alexander

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Issue DateTitleAuthor(s)Citation
2017Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1)Burns, Joshua; Day, John; et al, Various; Laura, Matilde; Lewis, Richard Alan; Li, Jun; Panosyan, Francis B.; Pisciotta, Chiara; Piscosquito, G; Rossor, Alexander; Yum, Sabrina; Clinical and Rehabilitation SciencesCross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1), Neurology, vol.89, 9, 2017,pp 927-935
2013Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic ParaplegiaClarke, Nigel; Menezes, Manoj; Oates, Emily; Auer-Grumbach, Michaela; Cottenie, Ellen; et al, Various; Foley, A Reghan; Gonzalez, Michael; Greensmith, Linda; Hafezparast, Majid; Houlden, Henry; Hurles, Matthew; Lek, Monkol; MacArthur, Daniel; Pieber, Thomas R; Rossor, Alexander; Scoto, Mariacristina; Speziani, Fiorella; Strom, Tim M; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthMutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia, American Journal of Human Genetics, vol.92, 6, 2013,pp 965-973
2015Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2Clarke, Nigel; Menezes, Manoj; North, Kathryn; Oates, Emily; Rodriguez, Michael; et al, Various; Gonzalez, Michael; Houlden, Henry; Liu, Yang; Murphy, Sinead; Phadke, Rahul; Rossor, Alexander; Salter, Hannah; Schule, Rebecca; Scoto, Mariacristina; Sewry, Caroline A; Childrens Hospital Westmead: Paediatrics & Child Health; Clinical and Rehabilitation Sciences; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; AnaesthesiaPhenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2, Brain, vol.138, 2, 2015,pp 293-310
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