Follow
Lucia Tedesco
Lucia Tedesco
ASST Monza
Verified email at asst-monza.it
Title
Cited by
Cited by
Year
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
802015
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
82017
Causal therapies in mucopolysaccharidoses: enzyme replacement therapy
A Vartanyan, AM Montaño
Journal of Child Science 8 (01), e156-e162, 2018
32018
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
22011
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
12005
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
The system can't perform the operation now. Try again later.
Articles 1–8