Browsing by Author Mastaglia, Frank

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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
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
2007Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's diseaseHalliday, Glenda; Rowe, Dominic; Sue, Carolyn; Vandebona, Himesha; Garlepp, Michael; Horne, Malcolm; Huang, Yue; Kotschet, Katya; Kwok, John B.J.; Mastaglia, Frank; Mellick, George; Rubio, Justin P.; Silburn, Peter A.; Stevens, Julia; Venn, Alison; Medicine Faculty Office; Northern Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Molecular Medicine (Kolling I)Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease, Movement Disorders (2005), vol.22,(7),2007,pp 982-989
2008Sporadic inclusion body myositis: Phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian casesCorbett, Alastair; Christiansen, F.; Day, T; James, I; Mastaglia, Frank; Needham, M; Phillips, B; Concord Clinical School: MedicineSporadic inclusion body myositis: Phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases, Journal of Neurology, Neurosurgery and Psychiatry, vol.79, N/A, 2008,pp 1056-1060