Browsing by Author Durr, Alexandra

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Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)Citation
2015Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegiaKennerson, Marina; Nicholson, Garth; Stoll, Marion; Charles, Perrine; Coutelier, Marie; Dionne-Laporte, Alexandre; Durr, Alexandra; et al, Various; Goizet, Cyril; Habarou, Florence; Jacoupy, Maxime; Konop, Juliette; Morais, Sara; Tao, Feifei; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteAlteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia, Brain, vol.138, 8, 2015,pp 2191-2205
2003A genome scan for modifiers of age at onset in Huntington Disease: The HD MAPS StudyTrent, Ronald; Almqvist, Elisabeth W; Brinkman, Ryan R; Dode, Catherine; Durr, Alexandra; Hayden, Michael R.; Li, Jian-Liang; Margolis, Russell L.; Morrison, Patrick J; Ross, Christopher A.; Suchowersky, Oksana; Central Clinical School: MedicineA genome scan for modifiers of age at onset in Huntington Disease: The HD MAPS Study, American Journal of Human Genetics, vol.73,(3),2003,pp 682-687
2006Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study.McCusker, Elizabeth; Trent, Ronald; Durr, Alexandra; et, al; Hayden, Michael R.; Li, Jian-Liang; Margolis, Russell L.; Morrison, Patrick J.; Nance, Martha; Rosenblatt, Adam; Ross, Christopher A.; Warby, Simon C.; Medicine; Central Clinical School: MedicineGenome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study., BMC Medical Genetics, vol.7,(N/A),2006,pp 71-71
2016Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task forceSue, Carolyn; Bertram, Lars; Durr, Alexandra; Ebrahimi-Fakhari, Darius; et al, Various; Lang, Anthony; Marras, Connie; Mercimek-Mahmutoglu, Saadet; Tabrizi, Sarah J.; van de Warrenburg, Bart P.; Warner, Thomas T.; Northern Clinical School: MedicineNomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force, Movement Disorders, vol.31, 4, 2016,pp 436-457
2015Variants associated with Gaucher disease in multiple system atrophyNicholson, Garth; Brice, Alexis; Durr, Alexandra; et al, Various; Kikuchi, Akio; Matsukawa, Takashi; Matsushima, Masaaki; Mitsui, Jun; Sasaki, Hidenao; Takashima, Hiroshi; Yabe, Ichiro; Concord Clinical School: ANZAC Research InstituteVariants associated with Gaucher disease in multiple system atrophy, Annals of Clinical and Translational Neurology, vol.2, 4, 2015,pp 417-426