Enzymatic replacement therapy for Hunter disease: Up to 9 years experience with 17 patients R Parini, M Rigoldi, L Tedesco, L Boffi, A Brambilla, S Bertoletti, ... Molecular genetics and metabolism reports 3, 65-74, 2015 | 80 | 2015 |
Body schema and corporeal self-recognition in the alien hand syndrome. E Olgiati, A Maravita, V Spandri, R Casati, F Ferraro, L Tedesco, ... Neuropsychology 31 (5), 575, 2017 | 8 | 2017 |
Causal therapies in mucopolysaccharidoses: enzyme replacement therapy A Vartanyan, AM Montaño Journal of Child Science 8 (01), e156-e162, 2018 | 3 | 2018 |
Effects of enzyme replacement therapy (ERT) on joint mobility in 27 patients (PTS) with mucopolysaccharidosis (MPS) I, II and VI F Furlan, M Rigoldi, F Santus, L Tedesco, R Parini Journal of Inherited Metabolic Disease 34, S207-S207, 2011 | 2 | 2011 |
284 Long-Term Outcome After Hematopoietic Stem Cell Transplantation (HCT) in Patients Affected by Mucopolysaccharidosis I Hurler (MPS IH) G Sersale, P Corti, G Uziel, L Tedesco, M Morbi, F Furlan, A Rovelli, ... Pediatric Research 58 (2), 403-403, 2005 | 1 | 2005 |
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome G Consiglieri, F Tucci, M De Pellegrin, B Guerrini, A Cattoni, G Risca, ... Science Translational Medicine 16 (745), eadi8214, 2024 | | 2024 |
Enzymatic replacement therapy in 17 patients affected by MPS I, II and VI M Rigoldi, L Tedesco, ML Melzi, A Lastrico, R Parini JOURNAL OF INHERITED METABOLIC DISEASE 31, 113-113, 2008 | | 2008 |
283 Treatment with Enzymatic Replacement Therapy (ERT) in Patients with Mucopolysaccharidosis Type I. Thirty Months Experience G Sersale, F Santus, F Furlan, M Rigoldi, F Menni, F Cichello, L Tedesco, ... Pediatric Research 58 (2), 403-403, 2005 | | 2005 |