Rossella Parini

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 12

Top Topics

Replacement Therapy

Allogeneic Hematopoietic Stem Cell Transplantation

Cross Sectional

Top Venues

Journal of inherited metabolic disease

Orphanet journal of rare diseases

Science translational medicine

Acta paediatrica (Oslo, Norway : 1992)

This page only lists publications with an associated author ORCID identifier.

Publications

Giulia Consiglieri, Francesca Tucci, Maurizio De Pellegrin, Barbara Guerrini, Alessandro Cattoni, Giulia Risca, Stefano Scarparo, Marina Sarzana, Silvia Pontesilli, Renata Mellone, Serena Gasperini, Stefania Galimberti, Paolo Silvani, Chiara Filisetti, Silvia Darin, Giulia Forni, Simona Miglietta, Ludovica Santi, Marcella Facchini, Ambra Corti, Francesca Fumagalli, Maria Pia Cicalese, Valeria Calbi, Maddalena Migliavacca, Federica Barzaghi, Francesca Ferrua, Vera Gallo, Salvatore Recupero, Daniele Canarutto, Matteo Doglio, Lucia Tedesco, Nicola Volpi, Attilio Rovelli, Giancarlo la Marca, Maria Grazia Valsecchi, Stefano Zancan, Fabio Ciceri, Luigi Naldini, Cristina Baldoli, Rossella Parini, Bernhard Gentner, Alessandro Aiuti, Maria Ester Bernardo
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome. Science translational medicine 16 (745) (2024)
Giulia Consiglieri, Francesca Tucci, Maurizio De Pellegrin, Barbara Guerrini, Alessandro Cattoni, Giulia Risca, Stefano Scarparo, Marina Sarzana, Silvia Pontesilli, Renata Mellone, Serena Gasperini, Stefania Galimberti, Paolo Silvani, Chiara Filisetti, Silvia Darin, Giulia Forni, Simona Miglietta, Ludovica Santi, Marcella Facchini, Ambra Corti, Francesca Fumagalli, Maria Pia Cicalese, Valeria Calbi, Maddalena Migliavacca, Federica Barzaghi, Francesca Ferrua, Vera Gallo, Salvatore Recupero, Daniele Canarutto, Matteo Doglio, Lucia Tedesco, Nicola Volpi, Attilio Rovelli, Giancarlo la Marca, Maria Grazia Valsecchi, Stefano Zancan, Fabio Ciceri, Luigi Naldini, Cristina Baldoli, Rossella Parini, Bernhard Gentner, Alessandro Aiuti, Maria Ester Bernardo
Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome. Science translational medicine 16 (745) (2024)
Federico Baronio, Stefano Zucchini, Francesco Zulian, Mariacarolina Salerno, Rossella Parini, Alessandro Cattoni, Federica Deodato, Alberto Gaeta, Carla Bizzarri, Serena Gasperini, Andrea Pession
Proposal of an Algorithm to Early Detect Attenuated Type I Mucopolysaccharidosis (MPS Ia) among Children with Growth Abnormalities. Medicina (Kaunas, Lithuania) 58 (1) (2022)
Rossella Parini, Guillem Pintos-Morell, Julia B Hennermann, Ting-Rong Hsu, Nesrin Karabul, Vasiliki Kalampoki, Andrey Gurevich, Uma Ramaswami, null null
Analysis of Renal and Cardiac Outcomes in Male Participants in the Fabry Outcome Survey Starting Agalsidase Alfa Enzyme Replacement Therapy Before and After 18 Years of Age. Drug design, development and therapy 14 (2020)
Rossella Parini, Federica Deodato
Intravenous Enzyme Replacement Therapy in Mucopolysaccharidoses: Clinical Effectiveness and Limitations. International journal of molecular sciences 21 (8) (2020)
Rodolfo Tonin, Anna Caciotti, Elena Procopio, Rita Fischetto, Federica Deodato, Maria Margherita Mancardi, Maja Di Rocco, Anna Ardissone, Alessandro Salviati, Antonio Marangi, Pietro Strisciuglio, Giusi Mangone, Arianna Casini, Silvia Ricci, Agata Fiumara, Rossella Parini, Francesco Saverio Pavone, Renzo Guerrini, Martino Calamai, Amelia Morrone
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content. Scientific reports 9 (1) (2019)
Giusy Ranucci, Miriam Rigoldi, Giovanna Cotugno, Silvia Maria Bernabei, Alessandra Liguori, Serena Gasperini, Bianca Maria Goffredo, Diego Martinelli, Lidia Monti, Paola Francalanci, Manila Candusso, Rossella Parini, Carlo Dionisi-Vici
Chronic liver involvement in urea cycle disorders. Journal of inherited metabolic disease 42 (6) (2019)
Anna Tylki-Szymańska, Linda De Meirleir, Maja Di Rocco, Waseem M Fathalla, Nathalie Guffon, Christina Lampe, Allan M Lund, Rossella Parini, Frits A Wijburg, Jiri Zeman, Maurizio Scarpa
Easy-to-use algorithm would provide faster diagnoses for mucopolysaccharidosis type I and enable patients to receive earlier treatment. Acta paediatrica (Oslo, Norway : 1992) 107 (8) (2019)
Alessandra Brambilla, Maria L Bianchi, Raffaella Cancello, Cinzia Galimberti, Serena Gasperini, Roberta Pretese, Miriam Rigoldi, Serena Tursi, Rossella Parini
Resting energy expenditure in argininosuccinic aciduria and in other urea cycle disorders. Journal of inherited metabolic disease 42 (6) (2019)
Rossella Parini, Paola De Lorenzo, Andrea Dardis, Alberto Burlina, Alessandra Cassio, Paolo Cavarzere, Daniela Concolino, Roberto Della Casa, Federica Deodato, Maria Alice Donati, Agata Fiumara, Serena Gasperini, Francesca Menni, Veronica Pagliardini, Michele Sacchini, Marco Spada, Roberta Taurisano, Maria Grazia Valsecchi, Maja Di Rocco, Bruno Bembi
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy. Orphanet journal of rare diseases 13 (1) (2018)
Rossella Parini, Alexander Broomfield, Maureen A Cleary, Linda De Meirleir, Maja Di Rocco, Waseem M Fathalla, Nathalie Guffon, Christina Lampe, Allan M Lund, Maurizio Scarpa, Anna Tylki-Szymańska, Jiří Zeman
International working group identifies need for newborn screening for mucopolysaccharidosis type I but states that existing hurdles must be overcome. Acta paediatrica (Oslo, Norway : 1992) 107 (12) (2018)
Rossella Parini, Federica Deodato, Maja Di Rocco, Edoardo Lanino, Franco Locatelli, Chiara Messina, Attilio Rovelli, Maurizio Scarpa
Open issues in Mucopolysaccharidosis type I-Hurler. Orphanet journal of rare diseases 12 (1) (2017)
Simon A Jones, Martin Bialer, Rossella Parini, Ken Martin, Hui Wang, Ke Yang, Adam J Shaywitz, Paul Harmatz
Safety and clinical activity of elosulfase alfa in pediatric patients with Morquio A syndrome (mucopolysaccharidosis IVA) less than 5 y. Pediatric research 78 (6) (2015)