Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature

B Schoser; E Fong; T Geberhiwot; D Hughes; JT Kissel; SC Madathil; D Orlikowski; MI Polkey; M Roberts; H.A.W.M. Tiddens; P Young

doi:10.1186/s13023-017-0598-0

Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature

B Schoser, E Fong, T Geberhiwot, D Hughes, JT Kissel, SC Madathil, D Orlikowski, MI Polkey, M Roberts, H.A.W.M. Tiddens, P Young

Pediatrics

Research output: Contribution to journal › Article › Academic › peer-review

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Original language	Undefined/Unknown
Article number	52
Journal	Orphanet Journal of Rare Diseases
Volume	12
DOIs	https://doi.org/10.1186/s13023-017-0598-0
Publication status	Published - 2017

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10.1186/s13023-017-0598-0

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http://hdl.handle.net/1765/98701

Cite this

Schoser, B., Fong, E., Geberhiwot, T., Hughes, D., Kissel, JT., Madathil, SC., Orlikowski, D., Polkey, MI., Roberts, M., Tiddens, H. A. W. M., & Young, P. (2017). Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature. Orphanet Journal of Rare Diseases, 12, [52]. https://doi.org/10.1186/s13023-017-0598-0

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Schoser, B, Fong, E, Geberhiwot, T, Hughes, D, Kissel, JT, Madathil, SC, Orlikowski, D, Polkey, MI, Roberts, M, Tiddens, HAWM & Young, P 2017, 'Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature', Orphanet Journal of Rare Diseases, vol. 12, 52. https://doi.org/10.1186/s13023-017-0598-0

TY - JOUR

T1 - Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature

AU - Schoser, B

AU - Fong, E

AU - Geberhiwot, T

AU - Hughes, D

AU - Kissel, JT

AU - Madathil, SC

AU - Orlikowski, D

AU - Polkey, MI

AU - Roberts, M

AU - Tiddens, H.A.W.M.

AU - Young, P

PY - 2017

Y1 - 2017

U2 - 10.1186/s13023-017-0598-0

DO - 10.1186/s13023-017-0598-0

M3 - Article

SN - 1750-1172

VL - 12

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

M1 - 52

ER -