The Second-Meal Phenomenon in Type 2 Diabetes

Por Jovanovic, Ana, Gerrard, Jean, Taylor, Roy
Publicado em 2009

Cultural diversity training for UK healthcare professionals: a comprehensive nationwide cross-sectional survey

Por Bentley, Paul, Jovanovic, Ana, Sharma, Pankaj
Publicado no Clin Med (Lond) (2008)

An atypical p.N215S variant of Fabry disease with end-stage renal failure

Por Sugarman, Max, Choudhury, Jamil, Jovanovic, Ana
Publicado no Mol Genet Metab Rep (2018)

Utilizing the Second-Meal Effect in Type 2 Diabetes: Practical Use of a Soya-Yogurt Snack

Por Chen, Mei Jun, Jovanovic, Ana, Taylor, Roy
Publicado em 2010

Examination of the correlations between forest fires and solar activity using Hurst index

Por Radovanović Milan, Vyklyuk Yaroslav, Jovanović Ana, Vuković Darko, Milenković Milan, Stevančević Milan, Matsiuk Nataliya
Publicado em 2013-01-01

Native T1 mapping versus CMR Feature Tracking (FT) derived strain analysis for the assessment of cardiac disease manifestation in Anderson Fabry

Por Reid, Anna B, Miller, Christopher A, Jovanovic, Ana, Woolfson, Peter, Abidin, Nik, Steeds, Richard P, Moon, James, Schmitt, Matthias
Publicado no J Cardiovasc Magn Reson (2016)

Enzyme replacement therapy and white matter hyperintensity progression in Fabry disease

Por Stefaniak, James D., Parkes, Laura M., Parry-Jones, Adrian R., Potter, Gillian M., Vail, Andy, Jovanovic, Ana, Smith, Craig J.
Publicado no Neurology (2018)

Haematopoietic Stem Cell Transplantation Arrests the Progression of Neurodegenerative Disease in Late-Onset Tay-Sachs Disease

Por Stepien, Karolina M., Lum, Su Han, Wraith, J. Edmond, Hendriksz, Christian J., Church, Heather J., Priestman, David, Platt, Frances M., Jones, Simon, Jovanovic, Ana, Wynn, Robert
Publicado no JIMD Rep (2017)

Improvement of Fabry Disease-Related Gastrointestinal Symptoms in a Significant Proportion of Female Patients Treated with Agalsidase Beta: Data from the Fabry Registry

Por Wilcox, William R., Feldt-Rasmussen, Ulla, Martins, Ana Maria, Ortiz, Alberto, Lemay, Roberta M., Jovanovic, Ana, Germain, Dominique P., Varas, Carmen, Nicholls, Katherine, Weidemann, Frank, Hopkin, Robert J.
Publicado no JIMD Rep (2017)

Phenotypic characteristics of the p.Asn215Ser (p.N215S) GLA mutation in male and female patients with Fabry disease: A multicenter Fabry Registry study

Por Germain, Dominique P., Brand, Eva, Burlina, Alessandro, Cecchi, Franco, Garman, Scott C., Kempf, Judy, Laney, Dawn A., Linhart, Aleš, Maródi, László, Nicholls, Kathy, Ortiz, Alberto, Pieruzzi, Federico, Shankar, Suma P., Waldek, Stephen, Wanner, Christoph, Jovanovic, Ana
Publicado no Mol Genet Genomic Med (2018)

Migalastat improves diarrhea in patients with Fabry disease: clinical-biomarker correlations from the phase 3 FACETS trial

Por Schiffmann, Raphael, Bichet, Daniel G., Jovanovic, Ana, Hughes, Derralynn A., Giugliani, Roberto, Feldt-Rasmussen, Ulla, Shankar, Suma P., Barisoni, Laura, Colvin, Robert B., Jennette, J. Charles, Holdbrook, Fred, Mulberg, Andrew, Castelli, Jeffrey P., Skuban, Nina, Barth, Jay A., Nicholls, Kathleen
Publicado no Orphanet J Rare Dis (2018)

Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry

Por Ortiz, Alberto, Abiose, Ademola, Bichet, Daniel G, Cabrera, Gustavo, Charrow, Joel, Germain, Dominique P, Hopkin, Robert J, Jovanovic, Ana, Linhart, Aleš, Maruti, Sonia S, Mauer, Michael, Oliveira, João P, Patel, Manesh R, Politei, Juan, Waldek, Stephen, Wanner, Christoph, Yoo, Han-Wook, Warnock, David G
Publicado no J Med Genet (2016)

Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study

Por Hughes, Derralynn A, Nicholls, Kathleen, Shankar, Suma P, Sunder-Plassmann, Gere, Koeller, David, Nedd, Khan, Vockley, Gerard, Hamazaki, Takashi, Lachmann, Robin, Ohashi, Toya, Olivotto, Iacopo, Sakai, Norio, Deegan, Patrick, Dimmock, David, Eyskens, François, Germain, Dominique P, Goker-Alpan, Ozlem, Hachulla, Eric, Jovanovic, Ana, Lourenco, Charles M, Narita, Ichiei, Thomas, Mark, Wilcox, William R, Bichet, Daniel G, Schiffmann, Raphael, Ludington, Elizabeth, Viereck, Christopher, Kirk, John, Yu, Julie, Johnson, Franklin, Boudes, Pol, Benjamin, Elfrida R, Lockhart, David J, Barlow, Carrolee, Skuban, Nina, Castelli, Jeffrey P, Barth, Jay, Feldt-Rasmussen, Ulla
Publicado no J Med Genet (2017)