Correction to: short and long-term acceptability and efficacy of extended-release cornstarch in the hepatic glycogen storage diseases: results from the Glyde study

Autor: DA Weinstein, RJ Jackson, EA Brennan, M Williams, JE Davison, F de Boer, TGJ Derks, C Ellerton, B Faragher, J Gribben, P Labrune, KM McKittrick, E Murphy, KM Ross, U Steuerwald, C Voillot, AJM Woodward, HR Mundy

Publikováno v: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-1 (2024)

Externí odkaz: https://doaj.org/article/466c5cfc8806414ea842936c98f452df

Short and long-term acceptability and efficacy of extended-release cornstarch in the hepatic glycogen storage diseases: results from the Glyde study.

Autor: Weinstein DA; Glycogen Storage Disease Program, Connecticut Childrens Medical Center, Hartford, USA. weinsteingsd@gmail.com.; School of Medicine, Department of Pediatrics, University of Connecticut, Farmington, CT, USA. weinsteingsd@gmail.com., Jackson RJ; Liverpool Clinical Trials Centre, University of LiverpoolUK, Liverpool, UK., Brennan EA; Vitaflo International Ltd, 182 Sefton Street, Liverpool, UK., Williams M; Glycogen Storage Disease Program, Connecticut Childrens Medical Center, Hartford, USA., Davison JE; Metabolic Medicine, Great Ormond Street Hospital, London, UK., Boer F; Division of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, Groningen, The Netherlands., Derks T; Division of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, Groningen, The Netherlands., Ellerton C; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Faragher B; Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, UK., Gribben J; Evelina London Childrens Hospital, Westminster Bridge Road, London, UK., Labrune P; Centre de Référence des Maladies héréditaires du Métabolisme Hépatique, APHP, Hôpitaux Universitaires Paris-Saclay, Hôpital Antoine Béclère, Clamart, and Paris-Saclay University, Paris, France., McKittrick KM; Vitaflo International Ltd, 182 Sefton Street, Liverpool, UK., Murphy E; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Ross KM; Glycogen Storage Disease Program, Connecticut Childrens Medical Center, Hartford, USA., Steuerwald U; National Hospital of the Faroe Islands, Medical Center, Tórshavn, Faroe Islands., Voillot C; Centre de Référence des Maladies héréditaires du Métabolisme Hépatique, APHP, Hôpitaux Universitaires Paris-Saclay, Hôpital Antoine Béclère, Clamart, and Paris-Saclay University, Paris, France., Woodward A; Evelina London Childrens Hospital, Westminster Bridge Road, London, UK., Mundy HR; Evelina London Childrens Hospital, Westminster Bridge Road, London, UK.

Publikováno v: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Jul 09; Vol. 19 (1), pp. 258. Date of Electronic Publication: 2024 Jul 09.