Výsledky vyhledávání - 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 Autor Paul Harmatz, Federica Cattaneo, Diego Ardigò, Silvia Geraci, Julia B. Hennermann, Nathalie Guffon, Allan M. Lund, Christian J. Hendriksz, Line Borgwardt
Vydáno 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 Autor Nathalie Guffon, Vassiliki Konstantopoulou, Julia B. Hennermann, Nicole Muschol, Irene Bruno, Albina Tummolo, Ferdinando Ceravolo, Giulia Zardi, Andrea Ballabeni, Allan M. Lund
Vydáno 2023Artigo -
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Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy Autor 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
Vydáno 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 Autor 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
Vydáno 2017Artigo -
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Defective hepatic bicarbonate production due to carbonic anhydrase VA deficiency leads to early-onset life-threatening metabolic crisis Autor 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
Vydáno 2016Artigo -
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Alpha-mannosidosis: correlation between phenotype, genotype and mutant MAN2B1 subcellular localisation Autor 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
Vydáno 2015Artigo -
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Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia Autor 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
Vydáno 2019Artigo -
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Correction to: Real-World Outcomes with Lomitapide Use in Paediatric Patients with Homozygous Familial Hypercholesterolaemia Autor 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
Vydáno 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 Autor 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
Vydáno 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... Autor 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
Vydáno 2018Artigo -
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Impact of age at onset and newborn screening on outcome in organic acidurias Autor 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
Vydáno 2015Artigo -
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Comprehensive long‐term efficacy and safety of recombinant human alpha‐mannosidase (velmanase alfa) treatment in patients with alpha‐mannosidosis Autor 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
Vydáno 2018Artigo -
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P486: A global Delphi consensus approach to monitoring and integrated care coordination of patients with alpha-mannosidosis Autor 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
Vydáno 2024Artigo -
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Monitoring and integrated care coordination of patients with alpha-mannosidosis: A global Delphi consensus study Autor 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
Vydáno 2024Artigo -
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Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease Autor 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
Vydáno 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... Autor 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
Vydáno 2006Revisão
Vyhledávací nástroje:
Související témata
Medicine
Internal medicine
Biology
Disease
Gene
Pediatrics
Genetics
Chemistry
Endocrinology
Mutation
Pathology
Alpha (finance)
Alternative medicine
Biochemistry
Clinical trial
Construct validity
Enzyme replacement therapy
Intensive care medicine
Nursing
Patient satisfaction
Amino acid
Gastroenterology
Genotype
Newborn screening
Phenotype
Physical therapy
Placebo
Surgery
Artificial intelligence
Asymptomatic