Fabry heterozygote mimicking multiple sclerosis

Por Yau, Wai Yan, Fabis-Pedrini, Marzena J, Kermode, Allan G
Publicado no BMJ Case Rep (2017)

Altered regulatory T-cell fractions and Helios expression in clinically isolated syndrome: clues to the development of multiple sclerosis

Por Jones, Anderson P, Trend, Stephanie, Byrne, Scott N, Fabis-Pedrini, Marzena J, Geldenhuys, Sian, Nolan, David, Booth, David R, Carroll, William M, Lucas, Robyn M, Kermode, Allan G, Hart, Prue H
Publicado no Clin Transl Immunology (2017)

Evolving Identification of Blood Cells Associated with Clinically Isolated Syndrome: Importance of Time since Clinical Presentation and Diagnostic MRI

Por Trend, Stephanie, Jones, Anderson P., Geldenhuys, Sian, Byrne, Scott N., Fabis-Pedrini, Marzena J., Nolan, David, Booth, David R., Carroll, William M., Lucas, Robyn M., Kermode, Allan G., Hart, Prue H.
Publicado no Int J Mol Sci (2017)

Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status

Por Binder, Michele D., Fox, Andrew D., Merlo, Daniel, Johnson, Laura J., Giuffrida, Lauren, Calvert, Sarah E., Akkermann, Rainer, Ma, Gerry Z. M., Perera, Ashwyn A., Gresle, Melissa M., Laverick, Louise, Foo, Grace, Fabis-Pedrini, Marzena J., Spelman, Timothy, Jordan, Margaret A., Baxter, Alan G., Foote, Simon, Butzkueven, Helmut, Kilpatrick, Trevor J., Field, Judith
Publicado no PLoS Genet (2016)