Browsing by Author Zhu, Danqing

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Issue DateTitleAuthor(s)Citation
2005Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.Kennerson, Marina; Nicholson, Garth; Walizada, Gina; Zhu, Danqing; Vance, J. M.; Züchner, Stephan; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Central Clinical School: Medicine; Concord Clinical School: MedicineCharcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations., NEUROLOGY 2005, vol.65,(3),2005,pp 496-497
2003CMT with pyramidal featuresKennerson, Marina; Kok, Cindy; Miedema, E; Nicholson, Garth; Vucic, Ostoja (Steve); Zhu, Danqing; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Central Clinical School: Medicine; Concord Clinical School: ANZAC Research Institute; Western Clinical School: Medicine (Westmead); Concord Clinical School: MedicineCMT with pyramidal features, Neurology, vol.60,(4),2003,pp 696-699
2009Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15Nicholson, Garth; Wei, Morgan; Zhu, Danqing; Bruno, Damien; Delatycki, Martin; Ganesamoorthy, Devika; Gardner, R. J. McKinlay; Schoumans, Jacqueline; Slater, Howard; Storey, Elsdon; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineDevelopment of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15, Clinical Chemistry (Washington, DC): international journal of molecular diagnostics and laboratory medicine, vol.55, 7,pp 1415-1418
2008Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations.Nicholson, Garth; Zhu, Danqing; Funalot, Benoit; Grew, S; Magdelaine, C; Ouvrier, Robert A.; Pollard, John D; Ryan, Monique M.; Vallat, Jean-Michel; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineHistopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations., Journal of neuropathology and experimental neurology, vol.67,(11),2008,pp 1097-1102
2015Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencingBrewer, Megan Hwa; Kennerson, Marina; Nicholson, Garth; Zhu, Danqing; Ahmad-Annuar, Azlina; Drew, Alexander P; Kidambi, Aditi; Ly, Carolyn; Tey, Shelisa; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineImproved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing, Molecular Genetics & Genomic Medicine, vol.3, 2, 2015,pp 143-154
2005Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.Kennerson, Marina; Nicholson, Garth; Walizada, Gina; Zhu, Danqing; Claeys, Kristl; De Jonghe, Peter; et, al; Merory, John; Noureddine, Maher; Oliveira, Sofia A.; Speer, Marcy C.; Stenger, Judith E.; Verhoeven, Kristien; Züchner, Stephan; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Central Clinical School: Medicine; Concord Clinical School: MedicineMutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease., Nature Genetics, vol.37,(3),2005,pp 289-294
2003Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the regionKennerson, Marina; Nicholson, Garth; Zhu, Danqing; Chrast, R; Lemke, G; Merory, John; Verheijen, M; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineRefined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region, Neurogenetics, vol.4,(4),2003,pp 179-183
2008Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutationsNicholson, Garth; Zhu, Danqing; Grew, S; Magdelaine, C; Ouvrier, Robert; Ryan, M; Sturtz, F; Vallat, Jean-Michel; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineSevere early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations, Neurology, vol.70, 19, 2008,pp 1678-1681