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Implementation Science Communications
|
August 26, 2025
Normalizing daily awakening and breathing coordination at 15 heterogenous ICUs: a multicenter post-implementation survey
Andrew J Knighton, Jacob Kean, Ithan D Peltan, et al.
JAMIA Open
|
July 11, 2022
An alert tool to promote lung protective ventilation for possible acute respiratory distress syndrome
Andrew J Knighton, Kathryn G Kuttler, Pallavi Ranade-Kharkar, et al.
American Journal of Human Genetics
|
October 23, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
Peter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
American Journal of Human Genetics
|
December 12, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
Peter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Research Square
|
October 16, 2023
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
David Picketts, Ghayda Mirzaa, Keqin Yan, et al.
Nature Communications
|
November 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
Ghayda M Mirzaa, Keqin Yan, Raissa Relator, et al.
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of 2
Search research articles
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Showing results (11-20 of 16) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 16 results.
Implementation Science Communications
|
August 26, 2025
Normalizing daily awakening and breathing coordination at 15 heterogenous ICUs: a multicenter post-implementation survey
Andrew J Knighton, Jacob Kean, Ithan D Peltan, et al.
JAMIA Open
|
July 11, 2022
An alert tool to promote lung protective ventilation for possible acute respiratory distress syndrome
Andrew J Knighton, Kathryn G Kuttler, Pallavi Ranade-Kharkar, et al.
American Journal of Human Genetics
|
October 23, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
Peter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
American Journal of Human Genetics
|
December 12, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
Peter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Research Square
|
October 16, 2023
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
David Picketts, Ghayda Mirzaa, Keqin Yan, et al.
Nature Communications
|
November 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
Ghayda M Mirzaa, Keqin Yan, Raissa Relator, et al.
Page
of 2