Browsing by Author Needham, Merrillee

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Issue DateTitleAuthor(s)Citation
2013Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositisCorbett, Alastair; Needham, Merrillee; Day, Timothy; James, I; Kiers, Lynette; Martinez, Patricia; Mastaglia, Frank; Mitrpant, Chalermchai; Rojana-udomsart, A.; Wilton, Steven D.; Witt, Campbell; Concord Clinical School: Medicine; Northern Clinical School: MedicineAnalysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis, Journal of Neuroimmunology, vol.254, 1-2, 2013,pp 174-177
2011The association of sporadic inclusion body myositis and Sjogren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotypeNeedham, Merrillee; Fabian, V.; Luo, Y.B.; Mastaglia, Frank; Rojana-udomsart, A.; Walters, S.; Zilko, P.J.; Northern Clinical School: MedicineThe association of sporadic inclusion body myositis and Sjogren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype, Clinical Neurology and Neurosurgery, vol.113, 7, 2011,pp 559-563
2011Axonal hyperpolarization in inclusion-body myopathy, paget disease of the bone, and frontotemporal dementia (IBMPFD)Burke, David; KUMAR, KISHORE R.; Liang, Christina; Needham, Merrillee; Ng, Karl; Sue, Carolyn; Central Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Kolling Institute; Northern Clinical School: Medicine; Central Clinical School: Medicine; Northern Clinical School: MedicineAxonal hyperpolarization in inclusion-body myopathy, paget disease of the bone, and frontotemporal dementia (IBMPFD), Muscle & Nerve, vol.44, 2, 2011,pp 191-196
2012High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: An analysis of disease-associated alleles and diplotypesCorbett, Alastair; Needham, Merrillee; Sue, Carolyn; Castley, Alison; Christiansen, F.; Day, T; James, I; Kiers, Lynette; Martinez, Patricia; Mastaglia, Frank; Rojana-udomsart, A.; Scott, Adrian; Witt, Campbell; Concord Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: MedicineHigh-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: An analysis of disease-associated alleles and diplotypes, Journal of Neuroimmunology, vol.250, 1-2, 2012,pp 77-82
2012Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositisNeedham, Merrillee; Allcock, R.; Dalakas, Marinos; Laing, Nigel G; Mastaglia, Frank; Scott, Adrian; Northern Clinical School: MedicineInvestigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis, Journal of Neuroimmunology, vol.250, 1-2, 2012,pp 66-70
2014Sickle cell disease and posterior reversible leukoencephalopathyGeevasinga, Nimeshan; Herkes, Geoffrey; Needham, Merrillee; Barnett, Yael; Cole, Catherine; Lin, Jamie; Western Clinical School: Medicine (Westmead); Pharmacy; Northern Clinical School: MedicineSickle cell disease and posterior reversible leukoencephalopathy, Journal of Clinical Neuroscience, vol.21, 8, 2014,pp 1329-1332