Medicine (University of Melbourne)

Organization name
Medicine (University of Melbourne)
Parent OrgUnit
City
Heidelberg, Victoria
Country
Australia


Results 941-960 of 1152 (Search time: 0.014 seconds).

Publication YearTitleAuthor(s)
9415-Sep-2016Endocrine Society of Australia position statement on male hypogonadism (part 2): treatment and therapeutic considerationsYeap, Bu B; Grossmann, Mathis ; McLachlan, Robert I; Handelsman, David J; Wittert, Gary A; Conway, Ann J; Stuckey, Bronwyn GA; Lording, Douglas W; Allan, Carolyn A; Zajac, Jeffrey D ; Burger, Henry G
942Sep-2016EHealth Technologies in Inflammatory Bowel Disease: A Systematic Review.Jackson, Belinda D ; Gray, Kathleen; Knowles, Simon R; De Cruz, Peter P 
943Sep-2016Hepatitis C-induced hepatocyte apoptosis following liver transplantation is enhanced by immunosuppressive agents.Lim, Eu Jin ; Chin, Ruth; Nachbur, U; Silke, J; Jia, Zhiyuan; Angus, Peter W ; Torresi, Joseph 
94411-Aug-2016A conceptualization of the utility of subjective cognitive decline in clinical trials of preclinical Alzheimer's diseaseBuckley, Rachel F; Villemagne, Victor L ; Masters, Colin L ; Ellis, Kathryn A; Rowe, Christopher C ; Johnson, Keith; Sperling, Reisa; Amariglio, Rebecca
945Aug-2016A randomised controlled trial of low-dose aspirin for the prevention of fractures in healthy older people: protocol for the ASPREE-Fracture substudy.Barker, Anna L; McNeil, John J; Seeman, Ego ; Ward, Stephanie A; Sanders, Kerrie M; Khosla, Sundeep; Cumming, Robert G; Pasco, Julie A; Bohensky, Megan A; Ebeling, Peter R; Woods, Robyn L; Lockery, Jessica E; Wolfe, Rory; Talevski, Jason
946Aug-2016Targeting advanced glycation with pharmaceutical agents: where are we now?Borg, Danielle J; Forbes, Josephine M
94714-Jul-2016Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicinePetrovski, Slavé; Goldstein, David B
948Jul-2016Subjective memory decline predicts greater rates of clinical progression in preclinical Alzheimer's disease.Buckley, Rachel F; Maruff, Paul; Ames, David; Bourgeat, Pierrick; Martins, Ralph N; Masters, Colin L ; Rainey-Smith, Stephanie R; Lautenschlager, Nicola; Rowe, Christopher C ; Savage, Greg; Villemagne, Victor L ; Ellis, Kathryn A
949Jul-2016Mosaic mutations in early-onset genetic diseases.Halvorsen, Matt; Petrovski, Slavé; Shellhaas, Renée; Tang, Yingying; Crandall, Laura; Goldstein, David; Devinsky, Orrin
950Jul-2016The role of the gut microbiota in NAFLDLeung, Christopher ; Rivera, L; Furness, John B; Angus, Peter W 
95123-Jun-2016Relationships between insulin resistance and frailty with body composition and testosterone in men undergoing androgen deprivation therapy for prostate cancerCheung, AS; Hoermann, R; Dupuis, P; Lim Joon, D ; Zajac, J ; Grossmann, M 
9521-Jun-2016Single-molecule sequencing reveals complex genomic variation of hepatitis B virus during 15 years of chronic infection following liver transplantationBetz-Stablein, BD; Töpfer, A; Littlejohn, M; Yuen, L; Colledge, D; Sozzi, V; Angus, Peter W ; Thompson, A; Revill, P; Beerenwinkel, N; Warner, N; Luciani, F
953Jun-2016Risk stratification in acute upper GI bleeding: comparison of the AIMS65 score with the Glasgow-Blatchford and Rockall scoring systemsRobertson, Marcus ; Majumdar, Avik; Boyapati, Ray; Chung, William ; Worland, Tom; Terbah, Ryma ; Wei, James; Lontos, Steve; Angus, Peter W ; Vaughan, Rhys B 
954Jun-2016Super-Resolution Track Density Imaging: Anatomic Detail versus Quantification.Calamante, Fernando
955Jun-2016Maximizing Patient Recruitment and Retention in a Secondary Stroke Prevention Clinical Trial: Lessons Learned from the STAND FIRM Study.Thayabaranathan, Tharshanah; Cadilhac, Dominique A; Srikanth, Velandai K; Fitzgerald, Sharyn M; Evans, Roger G; Kim, Joosup; Gerraty, Richard P; Phan, Thanh G; Bladin, Christopher F; Nelson, Mark R; Frayne, Judith H; Thrift, Amanda G
95614-May-2016Acute kidney disease and the communityKellum, John A; Ronco, Claudio; Bellomo, Rinaldo 
9575-May-2016Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.Petrovski, Slavé; Küry, Sébastien; Myers, Candace T; Anyane-Yeboa, Kwame; Cogné, Benjamin; Bialer, Martin; Xia, Fan; Hemati, Parisa; Riviello, James; Mehaffey, Michele; Besnard, Thomas; Becraft, Emily; Wadley, Alexandrea; Politi, Anya Revah; Colombo, Sophie; Zhu, Xiaolin; Ren, Zhong; Andrews, Ian; Dudding-Byth, Tracy; Schneider, Amy L ; Wallace, Geoffrey; Rosen, Aaron B I; Schelley, Susan; Enns, Gregory M; Corre, Pierre; Dalton, Joline; Mercier, Sandra; Latypova, Xénia; Schmitt, Sébastien; Guzman, Edwin; Moore, Christine; Bier, Louise; Heinzen, Erin L; Karachunski, Peter; Shur, Natasha; Grebe, Theresa; Basinger, Alice; Nguyen, Joanne M; Bézieau, Stéphane; Wierenga, Klaas; Bernstein, Jonathan A; Scheffer, Ingrid E ; Rosenfeld, Jill A; Mefford, Heather C; Isidor, Bertrand; Goldstein, David B
958May-2016Abnormal cognitive network interactions in Lennox-Gastaut syndrome: A potential mechanism of epileptic encephalopathy.Warren, Aaron E L; Abbott, David F ; Vaughan, David N; Jackson, Graeme D ; Archer, John S 
959Apr-2016A mutation in COL4A2 causes autosomal dominant porencephaly with cataracts.Ha, Thuong T; Sadleir, Lynette G; Mandelstam, Simone A; Paterson, Sarah J; Scheffer, Ingrid E ; Gecz, Jozef; Corbett, Mark A
960Apr-2016Interictal spikes and epileptic seizures: their relationship and underlying rhythmicityKaroly, Philippa J; Freestone, Dean R; Boston, Ray; Grayden, David B; Himes, David; Leyde, Kent; Seneviratne, Udaya; Berkovic, Samuel F ; O’Brien, Terence; Cook, Mark J