Christina Lampe

Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

Maurizio Scarpa, Zsuzsanna Almássy, Michael Beck et al. · Orphanet Journal of Rare Diseases · 2011 · 231 citations · Full text

Life Sciences, Neurology, Pathology +17

Measuring corneal clouding in patients suffering from mucopolysaccharidosis with the Pentacam densitometry programme

Heike M. Elflein, T Hofherr, F Berisha-Ramadani et al. · British Journal of Ophthalmology · 2013 · 76 citations

Life Sciences, Molecular Biology, Neuroscience +11

Importance of surgical history in diagnosing mucopolysaccharidosis type II (Hunter syndrome): Data from the Hunter Outcome Survey

Nancy J. Mendelsohn, Paul Harmatz, Olaf A. Bodamer et al. · Genetics in Medicine · 2010 · 75 citations

Medicine, Pathology, Surgical Pathology +2

Long‐term experience with enzyme replacement therapy (ERT) in MPS II patients with a severe phenotype: an international case series

Christina Lampe, Ann‐Kathrin Bosserhoff, Barbara K. Burton et al. · Journal of Inherited Metabolic Disease · 2014 · 71 citations · Full text

Life Sciences, Pharmacology, Pharmacotherapy +14

Clinical characteristics of adults with slowly progressing mucopolysaccharidosis VI: a case series

Anke Thümler, Elke Miebach, Christina Lampe et al. · Journal of Inherited Metabolic Disease · 2012 · 50 citations

Medicine, Pathology, Pediatrics +3