Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8)

Shahram Attarian; Peter Young; Thomas H. Brannagan; David Adams; Philip van Damme; Florian P. Thomas; Carlos Casanovas; Jafar Kafaie; C. line Tard; Maggie C. Walter; Yann Péréon; David Walk; Amro Stino; Marianne de Visser; Camiel Verhamme; Anthony Amato; Gregory Carter; Laurent Magy; Jeffrey M. Statland; Kevin Felice

doi:10.1186/s13023-024-03110-3

Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8)

Shahram Attarian, Peter Young, Thomas H. Brannagan, David Adams, Philip van Damme, Florian P. Thomas, Carlos Casanovas, Jafar Kafaie, C. line Tard, Maggie C. Walter, Yann Péréon, David Walk, Amro Stino, Marianne de Visser, Camiel Verhamme, Anthony Amato, Gregory Carter, Laurent Magy, Jeffrey M. Statland, Kevin Felice

Research output: Contribution to journal › Comment/Letter to the editor › Academic

Abstract

Following publication of the original article [1], we have been notified that we should add one more author to the authors’ group: Jafar Kafaie 8 8 Department of Neurology, Saint Louis University School of Medicine, St. Louis, USA The original article was updated.

Original language	English
Article number	142
Journal	Orphanet Journal of Rare Diseases
Volume	19
Issue number	1
DOIs	https://doi.org/10.1186/s13023-024-03110-3
Publication status	Published - 1 Dec 2024

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10.1186/s13023-024-03110-3

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Attarian, S., Young, P., Brannagan, T. H., Adams, D., van Damme, P., Thomas, F. P., Casanovas, C., Kafaie, J., Tard, C. L., Walter, M. C., Péréon, Y., Walk, D., Stino, A., de Visser, M., Verhamme, C., Amato, A., Carter, G., Magy, L., Statland, J. M., & Felice, K. (2024). Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8). Orphanet Journal of Rare Diseases, 19(1), Article 142. https://doi.org/10.1186/s13023-024-03110-3

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title = "Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8)",

abstract = "Following publication of the original article [1], we have been notified that we should add one more author to the authors{\textquoteright} group: Jafar Kafaie 8 8 Department of Neurology, Saint Louis University School of Medicine, St. Louis, USA The original article was updated.",

author = "Shahram Attarian and Peter Young and Brannagan, {Thomas H.} and David Adams and {van Damme}, Philip and Thomas, {Florian P.} and Carlos Casanovas and Jafar Kafaie and Tard, {C. line} and Walter, {Maggie C.} and Yann P{\'e}r{\'e}on and David Walk and Amro Stino and {de Visser}, Marianne and Camiel Verhamme and Anthony Amato and Gregory Carter and Laurent Magy and Statland, {Jeffrey M.} and Kevin Felice",

note = "Publisher Copyright: {\textcopyright} The Author(s) 2024.",

year = "2024",

month = dec,

day = "1",

doi = "10.1186/s13023-024-03110-3",

language = "English",

volume = "19",

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Attarian, S, Young, P, Brannagan, TH, Adams, D, van Damme, P, Thomas, FP, Casanovas, C, Kafaie, J, Tard, CL, Walter, MC, Péréon, Y, Walk, D, Stino, A, de Visser, M , Verhamme, C, Amato, A, Carter, G, Magy, L, Statland, JM & Felice, K 2024, 'Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8)', Orphanet Journal of Rare Diseases, vol. 19, no. 1, 142. https://doi.org/10.1186/s13023-024-03110-3

Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8). / Attarian, Shahram; Young, Peter; Brannagan, Thomas H. et al.
In: Orphanet Journal of Rare Diseases, Vol. 19, No. 1, 142, 01.12.2024.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Correction to

T2 - A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8)

AU - Attarian, Shahram

AU - Young, Peter

AU - Brannagan, Thomas H.

AU - Adams, David

AU - van Damme, Philip

AU - Thomas, Florian P.

AU - Casanovas, Carlos

AU - Kafaie, Jafar

AU - Tard, C. line

AU - Walter, Maggie C.

AU - Péréon, Yann

AU - Walk, David

AU - Stino, Amro

AU - de Visser, Marianne

AU - Verhamme, Camiel

AU - Amato, Anthony

AU - Carter, Gregory

AU - Magy, Laurent

AU - Statland, Jeffrey M.

AU - Felice, Kevin

PY - 2024/12/1

Y1 - 2024/12/1

N2 - Following publication of the original article [1], we have been notified that we should add one more author to the authors’ group: Jafar Kafaie 8 8 Department of Neurology, Saint Louis University School of Medicine, St. Louis, USA The original article was updated.

AB - Following publication of the original article [1], we have been notified that we should add one more author to the authors’ group: Jafar Kafaie 8 8 Department of Neurology, Saint Louis University School of Medicine, St. Louis, USA The original article was updated.

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U2 - 10.1186/s13023-024-03110-3

DO - 10.1186/s13023-024-03110-3

M3 - Comment/Letter to the editor

C2 - 38561848

SN - 1750-1172

VL - 19

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

IS - 1

M1 - 142

ER -

Attarian S, Young P, Brannagan TH, Adams D, van Damme P, Thomas FP et al. Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8). Orphanet Journal of Rare Diseases. 2024 Dec 1;19(1):142. doi: 10.1186/s13023-024-03110-3

Correction to: A double-blind, placebo-controlled, randomized trial of PXT3003 for the treatment of Charcot–Marie–Tooth type 1A (Orphanet Journal of Rare Diseases, (2021), 16, 1, (433), 10.1186/s13023-021-02040-8)

Abstract

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