Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021): Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to “TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases”) (Orphanet Journal of Rare Diseases, (2021), 16, 1, (62), 10.1186/s13023-020-01666-4)

SE Grimm; X Pouwels; BLT Ramaekers; B Wijnen; S Knies; Janneke P.C. Grutters; MA Joore

doi:10.1186/s13023-021-01938-7

Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021): Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to “TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases”) (Orphanet Journal of Rare Diseases, (2021), 16, 1, (62), 10.1186/s13023-020-01666-4)

SE Grimm^*, X Pouwels, BLT Ramaekers, B Wijnen, S Knies, Janneke P.C. Grutters, MA Joore

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic

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Original language	English
Article number	320
Journal	Orphanet Journal of Rare Diseases
Volume	16
DOIs	https://doi.org/10.1186/s13023-021-01938-7
Publication status	Published - 19 Jul 2021

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10.1186/s13023-021-01938-7Licence: CC BY

Grimm-2021-Correction-to-building-a-trusted-frFinal published version, 559 KBLicence: CC BY

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Grimm, SE., Pouwels, X., Ramaekers, BLT., Wijnen, B., Knies, S., Grutters, J. P. C., & Joore, MA. (2021). Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021): Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to “TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases”) (Orphanet Journal of Rare Diseases, (2021), 16, 1, (62), 10.1186/s13023-020-01666-4). Orphanet Journal of Rare Diseases, 16, [320]. https://doi.org/10.1186/s13023-021-01938-7

Grimm, SE ; Pouwels, X ; Ramaekers, BLT et al. / Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021) : Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to “TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases”) (Orphanet Journal of Rare Diseases, (2021), 16, 1, (62), 10.1186/s13023-020-01666-4). In: Orphanet Journal of Rare Diseases. 2021 ; Vol. 16.

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author = "SE Grimm and X Pouwels and BLT Ramaekers and B Wijnen and S Knies and Grutters, {Janneke P.C.} and MA Joore",

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Grimm, SE, Pouwels, X, Ramaekers, BLT, Wijnen, B, Knies, S, Grutters, JPC & Joore, MA 2021, 'Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021): Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to “TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases”) (Orphanet Journal of Rare Diseases, (2021), 16, 1, (62), 10.1186/s13023-020-01666-4)', Orphanet Journal of Rare Diseases, vol. 16, 320. https://doi.org/10.1186/s13023-021-01938-7

Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021) : Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to “TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases”) (Orphanet Journal of Rare Diseases, (2021), 16, 1, (62), 10.1186/s13023-020-01666-4). / Grimm, SE; Pouwels, X; Ramaekers, BLT et al.

In: Orphanet Journal of Rare Diseases, Vol. 16, 320, 19.07.2021.

Research output: Contribution to journal › Article › Academic

TY - JOUR

T1 - Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021)

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AU - Grimm, SE

AU - Pouwels, X

AU - Ramaekers, BLT

AU - Wijnen, B

AU - Knies, S

AU - Grutters, Janneke P.C.

AU - Joore, MA

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Grimm SE, Pouwels X, Ramaekers BLT, Wijnen B, Knies S, Grutters JPC et al. Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to " TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases") (vol 16, 62, 2021): Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to “TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases”) (Orphanet Journal of Rare Diseases, (2021), 16, 1, (62), 10.1186/s13023-020-01666-4). Orphanet Journal of Rare Diseases. 2021 Jul 19;16:320. doi: 10.1186/s13023-021-01938-7

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Building a trusted framework for uncertainty assessment in rare diseases: suggestions for improvement (Response to "TRUST4RD: tool for reducing uncertainties in the evidence generation for specialised treatments for rare diseases").

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