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Rheumatic Diseases Clinics of North America|April 20, 2013
Mucopolysaccharidoses and other lysosomal storage diseasesChristina Lampe, Cinzia Maria Bellettato, Nesrin Karabul, et al.Logopedics, Phoniatrics, Vocology|March 23, 2013
Alterations in speech and voice in patients with mucopolysaccharidosesTodsaporn Nakarat, Anne K Läßig, Christina Lampe, et al.Plos One|July 5, 2013
Illness perception and clinical treatment experiences in patients with M. Maroteaux-Lamy (mucopolysaccharidosis type VI) and a Turkish migration background in GermanyHansjörg Dilger, Linn Leissner, Lenka Bosanska, et al.Best Practice & Research. Clinical Endocrinology & Metabolism|May 20, 2015
Neuronopathic lysosomal storage disorders: Approaches to treat the central nervous systemMaurizio Scarpa, Cinzia Maria Bellettato, Christina Lampe, et al.Klinische Padiatrie|May 3, 2017
[Lysosomal Storage Diseases: Challenges in Multiprofessional Patient Care with Enzyme Replacement Therapy]Anibh Martin Das, Florian Lagler, Michael Beck, et al.Journal of Cell Science|May 16, 2019
Targeting specificity of nuclear-encoded organelle proteins with a self-assembling split-fluorescent protein toolkitMayank Sharma, Carola Kretschmer, Christina Lampe, et al.The Plant Journal : for Cell and Molecular Biology|December 30, 2017
The Xanthomonas effector XopL uncovers the role of microtubules in stromule extension and dynamics in Nicotiana benthamianaJessica L Erickson, Norman Adlung, Christina Lampe, et al.Journal of Inherited Metabolic Disease|February 15, 2013
Craniocervical decompression in patients with mucopolysaccharidosis VI: development of a scoring system to determine indication and outcome of surgeryChristina Lampe, Christian Lampe, Manfred Schwarz, et al.The Spine Journal : Official Journal of the North American Spine Society|April 13, 2018
Stand-alone craniocervical decompression is feasible in children with mucopolysaccharidosis type I, IVA, and VIHarald Krenzlin, Tan Ta-Chih, Christina Lampe, et al.Orphanet Journal of Rare Diseases|August 4, 2021
Social and medical needs of rare metabolic patients: results from a MetabERN surveySylvia Sestini, Laura Paneghetti, Christina Lampe, et al.Pageof 7