Illness Perception and Clinical Treatment Experiences in Patients with M. Maroteaux-Lamy (Mucopolysaccharidosis Type VI) and a Turkish Migration Background in Germany

por Dilger, Hansjörg, Leissner, Linn, Bosanska, Lenka, Lampe, Christina, Plöckinger, Ursula
Publicado 2013

Comparison of Rebound Tonometry, Perkins Applanation Tonometry and Ocular Response Analyser in Mucopolysaccharidosis Patients

por Wasielica-Poslednik, Joanna, Butsch, Christina, Lampe, Christina, Elflein, Heike, Lamparter, Julia, Weyer, Veronika, Pitz, Susanne
Publicado 2015

Social and medical needs of rare metabolic patients: results from a MetabERN survey

por Sestini, Sylvia, Paneghetti, Laura, Lampe, Christina, Betti, Gianni, Bond, Simon, Bellettato, Cinzia Maria, Maurizio, Scarpa
Publicado 2021

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

por Hendriksz, Christian J, Lavery, Christine, Coker, Mahmut, Ucar, Sema Kalkan, Jain, Mohit, Bell, Lisa, Lampe, Christina
Publicado 2014

The Inflammation in the Cytopathology of Patients With Mucopolysaccharidoses- Immunomodulatory Drugs as an Approach to Therapy

por Wiesinger, Anna-Maria, Bigger, Brian, Giugliani, Roberto, Scarpa, Maurizio, Moser, Tobias, Lampe, Christina, Kampmann, Christoph, Lagler, Florian B.
Publicado 2022

Heart and Cardiovascular Involvement in Patients with Mucopolysaccharidosis Type IVA (Morquio-A Syndrome)

por Kampmann, Christoph, Abu-Tair, Tariq, Gökce, Seyfullah, Lampe, Christina, Reinke, Jörg, Mengel, Eugen, Hennermann, Julia B., Wiethoff, Christiane M.
Publicado 2016

RETRACTED: An Innovative Tool for Evidence-Based, Personalized Treatment Trials in Mucopolysaccharidosis

por Wiesinger, Anna-Maria, Bigger, Brian, Giugliani, Roberto, Lampe, Christina, Scarpa, Maurizio, Moser, Tobias, Kampmann, Christoph, Zimmermann, Georg, Lagler, Florian B.
Publicado 2023

A conserved microtubule-binding region in Xanthomonas XopL is indispensable for induced plant cell death reactions

por Ortmann, Simon, Marx, Jolina, Lampe, Christina, Handrick, Vinzenz, Ehnert, Tim-Martin, Zinecker, Sarah, Reimers, Matthias, Bonas, Ulla, Erickson, Jessica Lee
Publicado 2023

RETRACTED: Wiesinger et al. An Innovative Tool for Evidence-Based, Personalized Treatment Trials in Mucopolysaccharidosis. Pharmaceutics 2023, 15, 1565

por Wiesinger, Anna-Maria, Bigger, Brian, Giugliani, Roberto, Lampe, Christina, Scarpa, Maurizio, Moser, Tobias, Kampmann, Christoph, Zimmermann, Georg, Lagler, Florian B.
Publicado 2023

Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countries

por Magner, Martin, Almássy, Zsuzsanna, Gucev, Zoran, Kieć-Wilk, Beata, Plaiasu, Vasilica, Tylki-Szymańska, Anna, Zafeiriou, Dimitrios, Zaganas, Ioannis, Lampe, Christina
Publicado 2022

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

por Lampe, Christina, Bosserhoff, Ann-Kathrin, Burton, Barbara K., Giugliani, Roberto, de Souza, Carolina F., Bittar, Camila, Muschol, Nicole, Olson, Rebecca, Mendelsohn, Nancy J.
Publicado 2014

Health-related quality of life in mucopolysaccharidosis: looking beyond biomedical issues

por Hendriksz, Christian J., Berger, Kenneth I., Lampe, Christina, Kircher, Susanne G., Orchard, Paul J., Southall, Rebecca, Long, Sarah, Sande, Stephen, Gold, Jeffrey I.
Publicado 2016

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

por Herzog, Andreas, Hartung, Ralf, Reuser, Arnold J J, Hermanns, Pia, Runz, Heiko, Karabul, Nesrin, Gökce, Seyfullah, Pohlenz, Joachim, Kampmann, Christoph, Lampe, Christina, Beck, Michael, Mengel, Eugen
Publicado 2012

Critical clinical situations in adult patients with Mucopolysaccharidoses (MPS)

por Stepien, Karolina M., Gevorkyan, Anait K., Hendriksz, Christian J., Lobzhanidze, Tinatin V., Pérez-López, Jordi, Tol, Govind, del Toro Riera, Mireia, Vashakmadze, Nato D., Lampe, Christina
Publicado 2020

Easy‐to‐use algorithm would provide faster diagnoses for mucopolysaccharidosis type I and enable patients to receive earlier treatment

por Tylki‐Szymańska, Anna, De Meirleir, Linda, Di Rocco, Maja, Fathalla, Waseem M., Guffon, Nathalie, Lampe, Christina, Lund, Allan M., Parini, Rossella, Wijburg, Frits A., Zeman, Jiri, Scarpa, Maurizio
Publicado 2018

Spinal involvement in mucopolysaccharidosis IVA (Morquio-Brailsford or Morquio A syndrome): presentation, diagnosis and management

por Solanki, Guirish A., Martin, Kenneth W., Theroux, Mary C., Lampe, Christina, White, Klane K., Shediac, Renée, Lampe, Christian G., Beck, Michael, Mackenzie, William G., Hendriksz, Christian J., Harmatz, Paul R.
Publicado 2013

International working group identifies need for newborn screening for mucopolysaccharidosis type I but states that existing hurdles must be overcome

por Parini, Rossella, Broomfield, Alexander, Cleary, Maureen A., De Meirleir, Linda, Di Rocco, Maja, Fathalla, Waseem M., Guffon, Nathalie, Lampe, Christina, Lund, Allan M., Scarpa, Maurizio, Tylki‐Szymańska, Anna, Zeman, Jiří
Publicado 2018

Mucopolysaccharidosis IVA (Morquio A syndrome) and VI (Maroteaux–Lamy syndrome): under-recognized and challenging to diagnose

por Lachman, Ralph S., Burton, Barbara K., Clarke, Lorne A., Hoffinger, Scott, Ikegawa, Shiro, Jin, Dong-Kyu, Kano, Hiroki, Kim, Ok-Hwa, Lampe, Christina, Mendelsohn, Nancy J., Shediac, Renée, Tanpaiboon, Pranoot, White, Klane K.
Publicado 2014

The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers

por Tylki-Szymańska, Anna, Almássy, Zsuzsanna, Christophidou-Anastasiadou, Violetta, Avdjieva-Tzavella, Daniela, Barisic, Ingeborg, Cerkauskiene, Rimante, Cuturilo, Goran, Djiordjevic, Maja, Gucev, Zoran, Hlavata, Anna, Kieć-Wilk, Beata, Magner, Martin, Pecin, Ivan, Plaiasu, Vasilica, Samardzic, Mira, Zafeiriou, Dimitrios, Zaganas, Ioannis, Lampe, Christina
Publicado 2022

The ethical framework for performing research with rare inherited neurometabolic disease patients

por Giannuzzi, Viviana, Devlieger, Hugo, Margari, Lucia, Odlind, Viveca Lena, Ragab, Lamis, Bellettato, Cinzia Maria, D’Avanzo, Francesca, Lampe, Christina, Cassis, Linda, Cortès-Saladelafont, Elisenda, Cazorla, Ángels Garcia, Barić, Ivo, Cvitanović-Šojat, Ljerka, Fumić, Ksenija, Dali, Christine I, Bartoloni, Franco, Bonifazi, Fedele, Scarpa, Maurizio, Ceci, Adriana
Publicado 2017