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Orphanet Journal of Rare Diseases|December 28, 2024
Impact of enzyme replacement therapy on clinical manifestations in females with Fabry diseaseMalte Lenders, Albina Nowak, Markus Cybulla, et al.Journal of Clinical Medicine|August 27, 2021
Disease Manifestations in Mucopolysaccharidoses and Their Impact on Anaesthesia-Related Complications-A Retrospective Analysis of 99 PatientsLuise Sophie Ammer, Thorsten Dohrmann, Nicole Maria Muschol, et al.Orphanet Journal of Rare Diseases|February 20, 2025
Impact of enzyme replacement therapy and migalastat on disease progression in females with fabry diseaseMalte Lenders, Albina Nowak, Markus Cybulla, et al.International Journal of Paediatric Dentistry|December 30, 2021
Mandibular condyle morphology among patients with mucopolysaccharidosis: An observational study of panoramic radiographsCarmen Ulrike Schmid-Herrmann, Nicole Maria Muschol, Vera Ulrike Fuhrmann, et al.Journal of Clinical Medicine|July 9, 2022
Anaesthesia-Relevant Disease Manifestations and Perianaesthetic Complications in Patients with Mucolipidosis-A Retrospective Analysis of 44 Anaesthetic Cases in 12 PatientsLuise Sophie Ammer, Nicole Maria Muschol, René Santer, et al.Journal of Orthopaedic Surgery and Research|March 20, 2021
Hip pathologies in mucopolysaccharidosis type IIISandra Rafaela Breyer, Eik Vettorazzi, Leonie Schmitz, et al.Molecular Genetics and Metabolism Reports|January 28, 2021
Is hematopoietic stem cell transplantation a therapeutic option for mucolipidosis type II?Luise Sophie Ammer, Sandra Pohl, Sandra Rafaela Breyer, et al.Journal of Clinical Medicine|June 28, 2023
CNS Manifestations in Mucolipidosis Type II-A Retrospective Analysis of Longitudinal Data on Neurocognitive Development and Neuroimaging in Eleven PatientsLuise Sophie Ammer, Karolin Täuber, Anna Perez, et al.Journal of Clinical Medicine|March 19, 2020
Hip Morphology in Mucolipidosis Type IILuise Sophie Ammer, Esmeralda Oussoren, Nicole Maria Muschol, et al.Pageof 2