Resultados da busca - Per Mathisen

Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency por Kristin Ørstavik, Kjell Arne Arntzen, Per Mathisen, Paul Hoff Backe, Trine Tangeraas, Magnhild Rasmussen, Erle Kristensen, Marijke Van Ghelue, Christoffer Jonsrud, Yngve Thomas Bliksrud

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The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease por Solrun Sigurdardottir, Birgitte Bjerkely, Trond G. Jenssen, Per Mathisen, Charlotte von der Lippe, Kristin Ørstavik, Ketil Heimdal, Dag Olav Dahle, Mina Susanne Weedon-Fekjær, Olga Solberg, Hege K. Pihlstrøm

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Health‐related quality of life in Norwegian adults with Fabry disease: Disease severity, pain, fatigue and psychological distress por Hege Kampen Pihlstrøm, Mina Susanne Weedon‐Fekjær, Birgitte Leisner Bjerkely, Charlotte von derLippe, Kristin Ørstavik, Per Mathisen, Ketil Heimdal, Trond Geir Jenssen, Dag Olav Dahle, Olga Karin Solberg, Solrun Sigurdardottir

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Can untreated PKU patients escape from intellectual disability? A systematic review por Danique van Vliet, Annemiek M. J. van Wegberg, Kirsten Ahring, Miroslaw Bik-Multanowski, Nenad Blau, Fatma D. Bulut, Kari Casas, Bozena Didycz, Maja Djordjevic, Antonio Federico, François Feillet, Maria Gizewska, Gwendolyn Gramer, Jozef L. Hertecant, Carla E. M. Hollak, Jens V. Jørgensen, Daniela Karall, Yuval Landau, Vincenzo Leuzzi, Per Mathisen, Kathryn Moseley, Neslihan Ö. Mungan, Francesca Nardecchia, Katrin Õunap, Kimberly K. Powell, Radha Ramachandran, Frank Rutsch, Aria Setoodeh, Maja Stojiljkovic, Fritz K. Trefz, Natalia Usurelu, Callum Wilson, Clara D. van Karnebeek, William B. Hanley, Francjan J. van Spronsen

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