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Rachel Thompson

Showing results (241-250 of 263) with videos related to

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Neoplasia (New York, N.Y.)|July 21, 2024
Epitranscriptomic mechanisms of androgen signalling and prostate cancerRodhan Patke, Anna E Harris, Corinne L Woodcock, et al.
European Journal of Human Genetics : EJHG|September 27, 2024
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseasesBerta Estévez-Arias, Leslie Matalonga, Delia Yubero, et al.
European Journal of Human Genetics : EJHG|December 10, 2024
Correction: Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseasesBerta Estévez-Arias, Leslie Matalonga, Delia Yubero, et al.
BMJ Evidence-Based Medicine|November 11, 2020
Ten papers for teachers of evidence-based medicine and health care: Sicily workshop 2019David Nunan, Adrienne Lindblad, Indah S Widyahening, et al.
BMJ Open|May 27, 2026
SAGE (safer analgesia): a protocol for a pragmatic cluster randomised controlled trial to reduce the use of high-risk medicines in people with chronic back and/or neck painChristina Abdel Shaheed, Andrew J McLachlan, Stephanie Mathieson, et al.
BMC Health Services Research|December 13, 2018
Standardized outcome measures for pregnancy and childbirth, an ICHOM proposalMalini Anand Nijagal, Stephanie Wissig, Caleb Stowell, et al.
Orphanet Journal of Rare Diseases|August 14, 2020
A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Orphanet Journal of Rare Diseases|March 23, 2021
Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Brain : a Journal of Neurology|February 19, 2025
Dominant rhabdomyolysis linked to a recurrent ATP2A2 variant reducing SERCA2 function in muscleSivasankar Malaichamy, Romane Idoux, Kiran Polavarapu, et al.
Med (New York, N.Y.)|November 14, 2023
The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human diseaseLeigh C Carmody, Michael A Gargano, Sabrina Toro, et al.
Pageof 27

Showing results (241-250 of 263) with videos related to

Sort By:
Pageof 27
Neoplasia (New York, N.Y.)|July 21, 2024
Epitranscriptomic mechanisms of androgen signalling and prostate cancerRodhan Patke, Anna E Harris, Corinne L Woodcock, et al.
European Journal of Human Genetics : EJHG|September 27, 2024
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseasesBerta Estévez-Arias, Leslie Matalonga, Delia Yubero, et al.
European Journal of Human Genetics : EJHG|December 10, 2024
Correction: Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseasesBerta Estévez-Arias, Leslie Matalonga, Delia Yubero, et al.
BMJ Evidence-Based Medicine|November 11, 2020
Ten papers for teachers of evidence-based medicine and health care: Sicily workshop 2019David Nunan, Adrienne Lindblad, Indah S Widyahening, et al.
BMJ Open|May 27, 2026
SAGE (safer analgesia): a protocol for a pragmatic cluster randomised controlled trial to reduce the use of high-risk medicines in people with chronic back and/or neck painChristina Abdel Shaheed, Andrew J McLachlan, Stephanie Mathieson, et al.
BMC Health Services Research|December 13, 2018
Standardized outcome measures for pregnancy and childbirth, an ICHOM proposalMalini Anand Nijagal, Stephanie Wissig, Caleb Stowell, et al.
Orphanet Journal of Rare Diseases|August 14, 2020
A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Orphanet Journal of Rare Diseases|March 23, 2021
Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a TreatabolomeAntonio Atalaia, Rachel Thompson, Alberto Corvo, et al.
Brain : a Journal of Neurology|February 19, 2025
Dominant rhabdomyolysis linked to a recurrent ATP2A2 variant reducing SERCA2 function in muscleSivasankar Malaichamy, Romane Idoux, Kiran Polavarapu, et al.
Med (New York, N.Y.)|November 14, 2023
The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human diseaseLeigh C Carmody, Michael A Gargano, Sabrina Toro, et al.
Pageof 27