• Leukocyte imbalances in Mucopolysaccharidoses patients 

      Lopes, Nuno; Maia, Maria L.; Pereira, Catia S.; Rodrigues, Inês Mondragão; Martins, Esmeralda; Ribeiro, Rosa; Gaspar, Ana; Aguiar, Patrício; Garcia, Paula; Cardoso, Maria Teresa; Rodrigues, Esmeralda; Teles, Elisa Leão; Giugliani, Roberto; Coutinho, Maria F.; Alves, Sandra; Macedo, Maria de Fátima Matos Almeida Henriques de (2023) [Artigo de periódico]
      Mucopolysaccharidoses (MPSs) are rare inherited lysosomal storage diseases (LSDs) caused by deficient activity in one of the enzymes responsible for glycosaminoglycans lysosomal degradation. MPS II is caused by pathogenic ...