Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ilkka Kantola"'
Autor:
Ilkka Kantola, Antti-Pekka Annala, Aki Hietaharju, Tiina M. Helioe, Taru-Tuuli Kantola, Johanna Kuusisto, Paivi Pietila Effati, Jukka Saarinen, Jyrki Taurio, Susanne Walls, Kati Valtola, Iina Yliaska
Publikováno v:
Molecular Genetics and Metabolism. 138:107176
Autor:
Paivi Pietila Effati, Jukka T. Saarinen, Eliisa Löyttyniemi, Maria Saarenhovi, Reijo Autio, Ilkka Kantola
Publikováno v:
Molecular Genetics and Metabolism. 138:107270
Publikováno v:
Molecular Genetics and Metabolism. 135:S97-S98
Autor:
Lorenzo Monserrat, Maurizio Pieroni, Dominique P. Germain, Michael Arad, Renzo Mignani, Derralynn Hughes, Ralf Baron, Victor Fomin, Frank Weidemann, Alberto Ortiz, Albina Nowak, Miguel Viana-Baptista, Marco Spada, Alessandro P. Burlina, Aleš Linhart, João Paulo Oliveira, Christoph Wanner, Ana Jovanovic, Ilkka Kantola, Ulla Feldt-Rasmussen, Perry M. Elliott, Camilla Tøndel, Mehdi Namdar, Anna Tylki-Szymańska, Max J. Hilz
Publikováno v:
Molecular Genetics and Metabolism. 124:189-203
Background Fabry disease, an inherited lysosomal storage disorder, causes multi-organ pathology resulting in substantial morbidity and a reduced life expectancy. Although Fabry disease is an X-linked disorder, both genders may be affected, but genera
Publikováno v:
Molecular Genetics and Metabolism. 129:S157-S158
Publikováno v:
Molecular Genetics and Metabolism. 129:S155
Autor:
Aki Hietaharju, Jukka T. Saarinen, Taru Kantola, Agneta Ekstrand, Kristiina Kananen, Antti-Pekka Annala, Jorma O. Kokkonen, Ilkka Kantola, Tiina Heliö, Miia Rainto, Jyrki Taurio, Lorenzo Sandini, Päivi Pietilä-Effati, Anne Karhu, Susanne Walls, Johanna Kuusisto, Iina Yliaska, Kati Valtola
Publikováno v:
Molecular Genetics and Metabolism. 129:S83
Autor:
Eva Brand, Ana Maria Martins, Dominique P. Germain, John L. Jefferies, Michael Mauer, Ulla Feldt-Rasmussen, Amel Karaa, Ilkka Kantola, William R. Wilcox, Meng Yang, Robert J. Hopkin, Ana Jovanovic, Nathalie Guffon, Han-Wook Yoo, Gustavo Cabrera
Publikováno v:
Molecular Genetics and Metabolism. 126:S73-S74
Fabry disease (FD) is a progressive X-linked disorder from deficiency of α-galactosidase and lysosomal accumulation of glycolipids. This Fabry Registry (NCT00196742) analysis assessed renal and cardiac outcomes of agalsidase beta treatment (1 mg/kg
Autor:
Pentti J. Tienari, Lorenzo Sandini, Antti-Pekka Annala, Kristiina Kananen, Agneta Ekstrand, Jorma O. Kokkonen, Päivi Pietilä-Effati, Kati Valtola, Aki Hietaharju, Susanne Walls, Anne Karhu, Jyrki Taurio, Iina Yliaska, Olavi Ukkola, Markku J. Savolainen, Johanna Kuusisto, Ilkka Kantola, Miia Rainto, Jukka T. Saarinen, Taru Kantola, Tiina Heliö
Publikováno v:
Molecular Genetics and Metabolism. 126:S81-S82
Enzyme replacement therapy (ERT) has stabilized renal function but its effect on proteinuria is inconsistent. Also nephroprotective renin-angiotensin-aldosterone system (RAAS) inhibition is warranted. We calculated eGFR using CKD-EPI formula and albu
Publikováno v:
Molecular Genetics and Metabolism. 126:S149