The Price of Really Clean Water: Combining Nanofiltration with Granular Activated Carbon and Anion Exchange Resins for the Removal of Per- And Polyfluoralkyl Substances (PFASs) in... von Franke, Vera, Ullberg, Malin, McCleaf, Philip, Wålinder, Maria, Köhler, Stephan J, Ahrens, Lutz

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Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 gen... von Olsson, K Sigvard, Wålinder, Olof, Jansson, Ulf, Wilbe, Maria, Bondeson, Marie-Louise, Stattin, Eva-Lena, Raha-Chowdhury, Ruma, Williams, Roger

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Burden of Treatment-Induced Peripheral Neuropathy in Patients with Multiple Myeloma in Sweden von Nahi, Hareth, Walinder, Göran, Patel, Vishal, Qu, Ying, Levine, Aaron, Majer, Istvan, Kutikova, Lucie, Hellqvist Franck, Eva, Svensson, Maria K., Hansson, Markus

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Common founder effects of hereditary hemochromatosis, Wilson's disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 gen... von Olsson, K. Sigvard, Wålinder, Olof, Jansson, Ulf, Wilbe, Maria, Bondeson, Marie-Louise, Stattin, Evalena, Raha-Chowdhury, Ruma, Williams, Roger

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Enantioselective analysis of citalopram and metabolites in adolescents von CARLSSON, Bjorn, OLSSON, Gunilla, REIS, Margareta, WALINDER, Jan, NORDIN, Conny, LUNDMARK, Jöns, SCORDO, Maria Gabriella, DAHL, Marja-Liisa, BENGTSSON, Finn, AHLNER, Johan

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Effect of Laundry Surfactants on Surface Charge and Colloidal Stability of Silver Nanoparticles von Skoglund, Sara, Lowe, Troy A, Hedberg, Jonas, Blomberg, Eva, Wallinder, Inger Odnevall, Wold, Susanna, Lundin, Maria

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Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 gen... von Olsson, K Sigvard, Wålinder, Olof, Jansson, Ulf, Wilbe, Maria, Bondeson, Marie-Louise, Stattin, Eva-Lena, Raha-Chowdhury, Ruma, Williams, Roger

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Common founder effects of hereditary hemochromatosis, Wilson's disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 gen... von Olsson, K. Sigvard, Wålinder, Olof, Jansson, Ulf, Wilbe, Maria, Bondeson, Marie-Louise, Stattin, Evalena, Raha-Chowdhury, Ruma, Williams, Roger

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Burden of Treatment-Induced Peripheral Neuropathy in Patients with Multiple Myeloma in Sweden von Nahi, Hareth, Walinder, Goran, Patel, Vishal, Qu, Ying, Levine, Aaron, Majer, Istvan, Kutikova, Lucie, Hellqvist Franck, Eva, Svensson, Maria K, Hansson, Markus

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