Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy
2007 · European Journal of Pediatrics · 516 citations
https://doi.org/10.1007/s00431-007-0635-4
A
Allan M. Lund
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Allan M. Lund is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Metabolism and Genetic Disorders & Lysosomal Storage Disorders Research & Connective tissue disorders research. The author has an h-index of 46, co-authored 246 publications.
ORCID: 0000-0002-6091-7879Papers by this author
worksMucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease
2011 · Orphanet Journal of Rare Diseases · 230 citations
https://doi.org/10.1186/1750-1172-6-72
Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III
2012 · Molecular Genetics and Metabolism · 102 citations
https://doi.org/10.1016/j.ymgme.2012.09.024
Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders
2016 · Journal of Inherited Metabolic Disease · 75 citations
https://doi.org/10.1007/s10545-016-9938-9
Enzyme replacement therapy with velmanase alfa (human recombinant alpha-mannosidase): Novel global treatment response model and outcomes in patients with alpha-mannosidosis
2018 · Molecular Genetics and Metabolism · 48 citations
https://doi.org/10.1016/j.ymgme.2018.04.003
Recognition of alpha-mannosidosis in paediatric and adult patients: Presentation of a diagnostic algorithm from an international working group
2019 · Molecular Genetics and Metabolism · 31 citations
https://doi.org/10.1016/j.ymgme.2019.01.024
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