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Erin Rothwell

Showing results (21-30 of 78) with videos related to

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Journal of Community Genetics|September 6, 2015
Life experiences of individuals with hereditary hemorrhagic telangiectasia and disclosing outside the family: a qualitative analysisLeigh Ann Higa, Jamie McDonald, Deborah O Himes, et al.
Pediatrics|March 30, 2011
State laws regarding the retention and use of residual newborn screening blood samplesMichelle H Lewis, Aaron Goldenberg, Rebecca Anderson, et al.
Journal of Pediatric Nursing|May 1, 2010
It's a small, small world: data collection strategies for research with children and adolescentsBecky J Christian, Patricia F Pearce, Anthony J Roberson, et al.
Familial Cancer|November 8, 2011
Patient outcomes associated with group and individual genetic counseling formatsErin Rothwell, Wendy Kohlmann, Kory Jasperson, et al.
Cancer Nursing|May 19, 2007
Perceptions of colon cancer screening by stage of screening test adoptionUsha Menon, Rhonda Belue, Celette Sugg Skinner, et al.
Journal of Community Genetics|December 6, 2013
Public attitudes regarding the use of electronic health information and residual clinical tissues for researchJeffrey R Botkin, Erin Rothwell, Rebecca Anderson, et al.
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|March 29, 2021
Women's Experiences With Palliative Care During PregnancyAndrea Crawford, Amelia Hopkin, Mary Rindler, et al.
BMJ Open|November 4, 2021
Lived experiences of patients with placenta accreta spectrum in Utah: a qualitative study of semi-structured interviewsBrett D Einerson, Melissa H Watt, Brittney Sartori, et al.
Journal of Community Genetics|February 4, 2015
Public attitudes regarding the use of electronic health information and residual clinical tissues for researchJeffrey R Botkin, Erin Rothwell, Rebecca Anderson, et al.
Ethics & Human Research|November 9, 2021
An Approach to Reviewing Local Context for Exception from Informed Consent Trials Using a Single IRBAnn R Johnson, Lisa M Rigtrup, John VanBuren, et al.
Pageof 8

Showing results (21-30 of 78) with videos related to

Sort By:
Pageof 8
Journal of Community Genetics|September 6, 2015
Life experiences of individuals with hereditary hemorrhagic telangiectasia and disclosing outside the family: a qualitative analysisLeigh Ann Higa, Jamie McDonald, Deborah O Himes, et al.
Pediatrics|March 30, 2011
State laws regarding the retention and use of residual newborn screening blood samplesMichelle H Lewis, Aaron Goldenberg, Rebecca Anderson, et al.
Journal of Pediatric Nursing|May 1, 2010
It's a small, small world: data collection strategies for research with children and adolescentsBecky J Christian, Patricia F Pearce, Anthony J Roberson, et al.
Familial Cancer|November 8, 2011
Patient outcomes associated with group and individual genetic counseling formatsErin Rothwell, Wendy Kohlmann, Kory Jasperson, et al.
Cancer Nursing|May 19, 2007
Perceptions of colon cancer screening by stage of screening test adoptionUsha Menon, Rhonda Belue, Celette Sugg Skinner, et al.
Journal of Community Genetics|December 6, 2013
Public attitudes regarding the use of electronic health information and residual clinical tissues for researchJeffrey R Botkin, Erin Rothwell, Rebecca Anderson, et al.
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|March 29, 2021
Women's Experiences With Palliative Care During PregnancyAndrea Crawford, Amelia Hopkin, Mary Rindler, et al.
BMJ Open|November 4, 2021
Lived experiences of patients with placenta accreta spectrum in Utah: a qualitative study of semi-structured interviewsBrett D Einerson, Melissa H Watt, Brittney Sartori, et al.
Journal of Community Genetics|February 4, 2015
Public attitudes regarding the use of electronic health information and residual clinical tissues for researchJeffrey R Botkin, Erin Rothwell, Rebecca Anderson, et al.
Ethics & Human Research|November 9, 2021
An Approach to Reviewing Local Context for Exception from Informed Consent Trials Using a Single IRBAnn R Johnson, Lisa M Rigtrup, John VanBuren, et al.
Pageof 8