Corrigendum: Newborn screening for X-linked adrenoleukodystrophy in Italy: diagnostic algorithm and disease monitoring

Eleonora Bonaventura; Luisella Alberti; Simona Lucchi; Laura Cappelletti; Salvatore Fazzone; Elisa Cattaneo; Matteo Bellini; Giana Izzo; Cecilia Parazzini; Alessandra Bosetti; Elisabetta Di Profio; Giulia Fiore; Matilde Ferrario; Chiara Mameli; Arianna Sangiorgio; Silvia Masnada; Gian Vincenzo Zuccotti; Pierangelo Veggiotti; Luigina Spaccini; Maria Iascone; Elvira Verduci; Cristina Cereda; Davide Tonduti; XALD-NBS Study Group

doi:10.3389/fneur.2024.1376447

Corrigendum: Newborn screening for X-linked adrenoleukodystrophy in Italy: diagnostic algorithm and disease monitoring

Front Neurol. 2024 Mar 6:15:1376447. doi: 10.3389/fneur.2024.1376447. eCollection 2024.

Authors

Eleonora Bonaventura^{1

2}, Luisella Alberti^{2

3}, Simona Lucchi³, Laura Cappelletti³, Salvatore Fazzone³, Elisa Cattaneo^{2

4}, Matteo Bellini⁵, Giana Izzo^{2

6}, Cecilia Parazzini^{2

6}, Alessandra Bosetti^{2

7}, Elisabetta Di Profio⁷, Giulia Fiore⁷, Matilde Ferrario^{2

7}, Chiara Mameli^{2

7

8}, Arianna Sangiorgio⁷, Silvia Masnada^{1

2}, Gian Vincenzo Zuccotti^{7

8}, Pierangelo Veggiotti^{1

2

8}, Luigina Spaccini^{2

4}, Maria Iascone⁵, Elvira Verduci^{2

7

9}, Cristina Cereda^{2

3}, Davide Tonduti^{1

2

8}; XALD-NBS Study Group

Collaborators

XALD-NBS Study Group:
Gianluca Lista, Paola Fontana, Tiziana Varisco, Olivia Casati, Alberto Fabio Podestà, Maddalena Gibelli, Stefano Martinelli, Roberta Restelli, Laura Maria Pogliani, Roberta Agistri, Marco Giuseppe Nedbal, Paolo Vaglia, Chryssoula Tzialla, Luisa Magnani, Elena Sala, Laura Lorioli, Giuseppe Banderali, Diana Ghisleni, Bruno Drera, Marta Frittoli, Francesca Lizzoli, Marta Bellini, Paola Bruni, Ilaria Giulini, Valentina Benedetti, Valentina Polimeni, Nadia Salvoni, Masotina Raffaele, Cristina Bellan, Roberto Bottino, Graziano Barera, Antonella Poloniato, Marta Odoni, Ilaria Dalla Verde, Massimo Agosti, Angela Bossi, Anna Tosi, Anna Elisabetta Bussolini, Francesco Maria Risso, Vania Spinoni, Nicola Altamura, Patrizia Ballista, Silvia Di Chio, Luciana Pagani, Lidia Decembrino, Michela Grignani, Grazia Morandi, Valeria Angela Fasolato, Lorella Rossi, Emilio Palumbo, Alessandro Lepore, Maria Forestieri, Stefano Ghirardello, Elisa Civardi, Paolo Adamoli, Roberta Giacchero, Giovanni Traina, Patrizia Calzi, Fenesia Pedace, Marco Sala

Affiliations

¹ Child Neurology Unit, V. Buzzi Children's Hospital, Milan, Italy.
² Center for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
³ Newborn Screening and Inherited Metabolic Disease Unit, V. Buzzi Children Hospital, Milan, Italy.
⁴ Clinical Genetics Unit, V. Buzzi Children's Hospital, Milan, Italy.
⁵ Molecular Genetics Laboratory, ASST Papa Giovanni XXIII, Bergamo, Italy.
⁶ Paediatric Radiology and Neuroradiology Department, V. Buzzi Children's Hospital, Milan, Italy.
⁷ Department of Paediatrics, V. Buzzi Children's Hospital, University of Milan, Milan, Italy.
⁸ Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
⁹ Department of Health Sciences, University of Milan, Milan, Italy.

Abstract

[This corrects the article DOI: 10.3389/fneur.2022.1072256.].

Keywords: Aicardi-Goutières syndrome (AGS); C26:0-lysophosphatidylcholine; DBS; X-ALD; X-linked adrenoleukodystrophy (X-ALD); Zellweger Spectrum Disorders; hematopoietic stem cell transplantation (HCST); newborn screening (NBS).

Copyright © 2024 Bonaventura, Alberti, Lucchi, Cappelletti, Fazzone, Cattaneo, Bellini, Izzo, Parazzini, Bosetti, Di Profio, Fiore, Ferrario, Mameli, Sangiorgio, Masnada, Zuccotti, Veggiotti, Spaccini, Iascone, Verduci, Cereda, Tonduti and XALD-NBS Study Group.

Publication types

Published Erratum