Search Results - Allan M. Lund
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Enzyme replacement therapy with velmanase alfa (human recombinant alpha-mannosidase): Novel global treatment response model and outcomes in patients with alpha-mannosidosis by Paul Harmatz, Federica Cattaneo, Diego Ardigò, Silvia Geraci, Julia B. Hennermann, Nathalie Guffon, Allan M. Lund, Christian J. Hendriksz, Line Borgwardt
Published 2018Artigo -
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Long‐term safety and efficacy of velmanase alfa treatment in children under 6 years of age with alpha‐mannosidosis: A phase 2, open label, multicenter study by Nathalie Guffon, Vassiliki Konstantopoulou, Julia B. Hennermann, Nicole Muschol, Irene Bruno, Albina Tummolo, Ferdinando Ceravolo, Giulia Zardi, Andrea Ballabeni, Allan M. Lund
Published 2023Artigo -
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Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy by J. E. Wraith, Maurizio Scarpa, Michael Beck, Olaf A. Bodamer, Linda De Meırleır, Nathalie Guffon, Allan M. Lund, Gunilla Malm, Ans T. van der Ploeg, J Zeman
Published 2007Revisão -
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Hyperglucagonemia correlates with plasma levels of non-branched-chain amino acids in patients with liver disease independent of type 2 diabetes by Nicolai J. Wewer Albrechtsen, Anders Junker, Mette Christensen, Sofie Hædersdal, Flemming Wibrand, Allan M. Lund, Katrine D. Galsgaard, Jens J. Holst, Filip K. Knop, Tina Vilsbøll
Published 2017Artigo -
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Defective hepatic bicarbonate production due to carbonic anhydrase VA deficiency leads to early-onset life-threatening metabolic crisis by Carmen Dı́ez-Fernández, Véronique Rüfenacht, Saikat Santra, Allan M. Lund, René Santer, Martin Lindner, Trine Tangeraas, Caroline Unsinn, Pascale de Lonlay, Alberto Burlina, Clara van Karnebeek, Johannes Häberle
Published 2016Artigo -
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Alpha-mannosidosis: correlation between phenotype, genotype and mutant MAN2B1 subcellular localisation by Line Borgwardt, Hilde Monica Frostad Riise Stensland, Klaus J Olsen, Flemming Wibrand, Helle Bagterp Klenow, Michael Beck, Yasmina Amraoui, Laila Arash, J. Fogh, Øivind Nilssen, Christine í Dali, Allan M. Lund
Published 2015Artigo -
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Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia by Tawfeg Ben‐Omran, L. Masana, Genovefa Kolovou, Gema Ariceta, Francisco J. Nóvoa, Allan M. Lund, Martin P. Bogsrud, Maria Lúcia Góes Araujo, Osamah Hussein, Daiana Ibarretxe, Rosa M. Sanchez-Hernández, Raúl D. Santos
Published 2019Artigo -
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Correction to: Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia by Tawfeg Ben‐Omran, L. Masana, Genovefa Kolovou, Gema Ariceta, Francisco J. Nóvoa, Allan M. Lund, Martin P. Bogsrud, Maria Lúcia Góes Araujo, Osamah Hussein, Daiana Ibarretxe, Rosa M. Sanchez-Hernández, Raúl D. Santos
Published 2024Errata/Corrigenda -
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Evolution of mobility, pain/discomfort, self-care, and mental health in patients with alpha-mannosidosis: an international caregiver and patient survey by Karolina M. Stępień, Sophie Thomas, Julia B. Hennermann, Christina Lampe, Nicole Muschol, Maria Juliana Ballesta-Martínez, José Ramiro Cruz, M. López Rodríguez, Anneliese Lopes Barth, Martin Magner, Allan M. Lund, Vasilica Plăiaşu, Andrea Ballabeni, Francesca Donà, Heather Morgan, Nathalie Guffon
Published 2025Artigo -
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Efficacy and safety of Velmanase alfa in the treatment of patients with alpha‐mannosidosis: results from the core and extension phase analysis of a phase III multicentre, double‐bl... by Line Borgwardt, Nathalie Guffon, Yasmina Amraoui, Christine í Dali, Linda De Meırleır, Mercedes Gil‐Campos, Bénédicte Héron, Silvia Geraci, Diego Ardigò, Federica Cattaneo, J. Fogh, J. M. Hannerieke Van den Hout, Michael Beck, Simon Jones, Anna Tylki‐Szymańska, Ulla Haugsted, Allan M. Lund
Published 2018Artigo -
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Impact of age at onset and newborn screening on outcome in organic acidurias by Jana Herınger, Vassili Valayannopoulos, Allan M. Lund, Frits A. Wijburg, Peter Freisinger, Ivo Barić, Matthias R. Baumgartner, Peter Burgard, Alberto Burlina, Kimberly A. Chapman, Elisenda Cortès i Saladelafont, Daniela Karall, Chris Mühlhausen, Victoria Riches, Manuel Schiff, Jolanta Sykut‐Cegielska, John H. Walter, Jiri Zeman, B. Chabrol, Stefan Kölker
Published 2015Artigo -
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Comprehensive long‐term efficacy and safety of recombinant human alpha‐mannosidase (velmanase alfa) treatment in patients with alpha‐mannosidosis by Allan M. Lund, Line Borgwardt, Federica Cattaneo, Diego Ardigò, Silvia Geraci, Mercedes Gil‐Campos, Linda De Meırleır, Cécile Laroche, Philippe Dolhem, Duncan Cole, Anna Tylki‐Szymańska, M. López Rodríguez, Encarna Guillén‐Navarro, Christine í Dali, Bénédicte Héron, J. Fogh, Nicole Muschol, Dawn Phillips, J. M. Hannerieke Van den Hout, Simon Jones, Yasmina Amraoui, Paul Harmatz, Nathalie Guffon
Published 2018Artigo -
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P486: A global Delphi consensus approach to monitoring and integrated care coordination of patients with alpha-mannosidosis by Can Fıçıcıoğlu, Nicole Muschol, Barbara K. Burton, Martin Magner, Mercedes Gil‐Campos, M. López Rodríguez, Parul Jayakar, Allan M. Lund, Galit Tal, José Elías García‐Ortíz, Karolina M. Stępień, Carolyn Ellaway, Walla Al‐Hertani, Roberto Giugliani, Sara Cathey, Julia B. Hennermann, Christina Lampe, Markey McNutt, Florian B. Lagler, Maurizio Scarpa, V. Reid Sutton, Nathalie Guffon
Published 2024Artigo -
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Monitoring and integrated care coordination of patients with alpha-mannosidosis: A global Delphi consensus study by Nathalie Guffon, Barbara K. Burton, Can Fıçıcıoğlu, Martin Magner, Mercedes Gil‐Campos, Monica A. Lopez-Rodriguez, Parul Jayakar, Allan M. Lund, Galit Tal, José Elías García‐Ortíz, Karolina M. Stępień, Carolyn Ellaway, Walla Al‐Hertani, Roberto Giugliani, Sara Cathey, Julia B. Hennermann, Christina Lampe, Markey McNutt, Florian B. Lagler, Maurizio Scarpa, V. Reid Sutton, Nicole Muschol
Published 2024Artigo -
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Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease by Maurizio Scarpa, Zsuzsanna Almássy, Michael Beck, Olaf A. Bodamer, Iain Bruce, Linda De Meırleır, Nathalie Guffon, Encarna Guillén‐Navarro, Pauline Hensman, Simon Jones, Wolfgang Kamin, Christoph Kampmann, Christina Lampe, Christine Lavery, Elisa Leão Teles, Bianca Link, Allan M. Lund, Gunilla Malm, Susanne Pitz, Michael Rothera, Catherine Stewart, Anna Tylki‐Szymańska, Ans van der Ploeg, Robert Walker, J Zeman, J. E. Wraith
Published 2011Artigo -
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Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and prot... by Joan C. Marini, Antonella Forlino, Wayne A. Cabral, Aileen M. Barnes, James D. San Antonio, Sarah A. Milgrom, James Hyland, Jarmo Körkkö, Darwin J. Prockop, Anne De Paepe, Paul Coucke, Sofie Symoens, Francis H. Glorieux, Peter J. Roughley, Allan M. Lund, Kaija Kuurila-Svahn, Heini Hartikka, Daniel H. Cohn, Deborah Krakow, Monica Mottes, Ulrike Schwarze, Diana Chen, Kathleen Yang, Christine Kuslich, James Troendle, Raymond Dalgleish, Peter H. Byers
Published 2006Revisão
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