Browsing by Author Sue, Carolyn

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Issue DateTitleAuthor(s)Citation
2013Fibroblast growth factor 21 is a sensitive biomarker of mitochondrial diseaseDavis, Ryan; Liang, Christina; Sue, Carolyn; Edema-Hildebrand, Fabienne; Needham, Merrilee; Riley, Catherine; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineFibroblast growth factor 21 is a sensitive biomarker of mitochondrial disease, Neurology, vol.81, 21, 2013,pp 1819-1826
2012Frequency of the D620N mutation in VPS35 in Parkinson diseaseKumar, Kishore Raj; Sue, Carolyn; et al, Various; Heldmann, Marcus; Kasten, Meike; Kostic, Vladimir S; Ramirez, Alfredo; Segura-Aguilar, Juan; Simon, David K; Svetel, Marina; Tunc, Sinem; Vieregge, Peter; Weissbach, Anne; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineFrequency of the D620N mutation in VPS35 in Parkinson disease, JAMA Neurology, vol.69, 10, 2012,pp 1360-1364
2012Frequency of the D620N mutation in VPS35 in Parkinson diseaseKumar, Kishore Raj; Sue, Carolyn; et al, Various; Heldmann, Marcus; Kasten, Meike; Kostic, Vladimir S; Ramirez, Alfredo; Segura-Aguilar, Juan; Simon, David K; Svetel, Marina; Tunc, Sinem; Vieregge, Peter; Weissbach, Anne; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineFrequency of the D620N mutation in VPS35 in Parkinson disease, JAMA Neurology, vol.69, 10, 2012,pp 1360-1364
2007A functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's diseaseRowe, Dominic; Sue, Carolyn; Chan, Daniel K. Y.; Halliday, Glenda M.; Mellick, George; Silburn, Peter; Sutherland, Greg; Northern Clinical School: Medicine; Northern Clinical School: MedicineA functional polymorphism in the parkin gene promoter affects the age of onset of Parkinson's disease, Neuroscience Letters (2005), vol.414,(2),2007,pp 170-173
2011The genetics of mitochondrial diseaseDavis, Ryan; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineThe genetics of mitochondrial disease, Seminars in Neurology, vol.31, 5, 2011,pp 519-530
2013Glucocerebrosidase mutations in a Serbian Parkinson's disease populationKumar, Kishore Raj; Sue, Carolyn; Alcalay, Roy N; Gobel, Anna; Grunewald, A; Klein, Christine; Kostic, Vladimir S; Krainc, Dimitri; Kresojevic, Nikola D; Lohmann, Katja; Mazzulli, Joseph R; Ramirez, Alfredo R; Rolfs, Arndt; Svetel, Marina; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineGlucocerebrosidase mutations in a Serbian Parkinson's disease population, European Journal of Neurology, vol.20, 2, 2013,pp 402-405
2017Hereditary parkinsonism-associated genetic variations in PARK9 locus lead to functional impairment of ATPase type 13A2Park, Jin-Sung; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineHereditary parkinsonism-associated genetic variations in PARK9 locus lead to functional impairment of ATPase type 13A2, Current Protein and Peptide Science, vol.18, 1, 2017,pp 725-732
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
2016Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell modelsDavis, Ryan; Koentjoro, Brianada; Park, Jin-Sung; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineLoss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models, Parkinsonism and Related Disorders, vol.27, N/A, 2016,pp 67-73
2016Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell modelsDavis, Ryan; Koentjoro, Brianada; Park, Jin-Sung; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineLoss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models, Parkinsonism and Related Disorders, vol.27, N/A, 2016,pp 67-73
2014Low dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic ParaplegiaSue, Carolyn; Bellette, Bernadette; Crane, Denis I.; Fan, Yongiun; Mackay-Sim, Alan; Sutharsan, Ratneswary; Wali, Gautam; Northern Clinical School: MedicineLow dose tubulin-binding drugs rescue peroxisome trafficking deficit in patient-derived stem cells in Hereditary Spastic Paraplegia, Biology Open, vol.3, 6, 2014,pp 494-502
2006Measurement of ATP production in mitochondrial disorders.Shepherd, R; Sue, Carolyn; Checcarelli, N; De, V v; DiMauro, Salvatore; Naini, A; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: MedicineMeasurement of ATP production in mitochondrial disorders., Journal of inherited metabolic disease, vol.29,(1),2006,pp 86-91
2011Mechanical Thrombectomy with a Self-Expanding Retrievable Intracranial Stent (Solitaire AB): Experience in 26 Patients with Acute Cerebral Artery OcclusionSue, Carolyn; Faulder, Kenneth Charles; Goh, A. C. C.; Harrington, Tim; Miteff, F.; Steinfort, B. S.; Northern Clinical School: MedicineMechanical Thrombectomy with a Self-Expanding Retrievable Intracranial Stent (Solitaire AB): Experience in 26 Patients with Acute Cerebral Artery Occlusion, American Journal Of Neuroradiology, vol.32, 6, 2011,pp 1078-1081
2016Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic ParaplegiaSue, Carolyn; Crane, Denis I; Fan, Yongjun; Mackay-Sim, Alan; Stewart, Romal; Sutharsan, Ratneswary; Velasquez, Johana Tello; Wali, Gautam; Northern Clinical School: MedicineMechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia, Scientific Reports, vol.6, N/A, 2016,pp 1-14
2004MELAS A3243G Mitochondrial DNA Mutation And Age Related MaculopathyJones, Michael; Mitchell, Paul (Ronald); Sue, Carolyn; Wang, Jie Jin; Clinical Schools; Western Clinical School: Westmead Millennium Institute; Northern Clinical School: Medicine; Western Clinical School: Westmead Millennium InstituteMELAS A3243G Mitochondrial DNA Mutation And Age Related Maculopathy, American Journal of Ophthalmology, vol.138,(6),2004,pp 1051-1053
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141
2018Mitochondrial diseasesDavis, Ryan; Liang, Christina; Sue, Carolyn; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMitochondrial diseases, Handbook of Clinical Neurology, vol.147, N/A, 2018,pp 125-141