Christina Lampe

Natural history and galsulfase treatment in mucopolysaccharidosis VI (MPS VI, Maroteaux–Lamy syndrome)—10‐year follow‐up of patients who previously participated in an MPS VI survey study

Roberto Giugliani, Christina Lampe, Nathalie Guffon et al. · American Journal of Medical Genetics Part A · 2014 · 98 citations · Full text

Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey

Christian J. Hendriksz, Christine Lavery, Mahmut Çöker et al. · Orphanet Journal of Rare Diseases · 2014 · 92 citations · Full text

A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations

Andreas Herzog, Ralf Hartung, Arnold Reuser et al. · Orphanet Journal of Rare Diseases · 2012 · 88 citations · Full text

Design, baseline characteristics, and early findings of the MPS VI (mucopolysaccharidosis VI) Clinical Surveillance Program (CSP)

Christian J. Hendriksz, Roberto Giugliani, Paul Harmatz et al. · Journal of Inherited Metabolic Disease · 2011 · 65 citations

The <i>Xanthomonas</i> effector XopL uncovers the role of microtubules in stromule extension and dynamics in <i>Nicotiana benthamiana</i>

Jessica Lee Erickson, Norman Adlung, Christina Lampe et al. · The Plant Journal · 2017 · 59 citations · Full text