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Philip Lee

Showing results (21-30 of 128) with videos related to

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Qualitative Health Research|August 21, 2015
Talking About Looking: Three Approaches to Interviewing Carers of People With Rheumatoid Arthritis About Information SeekingRichard Philip Lee, Ben Thompson, Paul Whybrow, et al.
Biomedical Microdevices|February 24, 2006
Microfluidic alignment of collagen fibers for in vitro cell culturePhilip Lee, Rob Lin, James Moon, et al.
Food Science & Nutrition|October 12, 2023
Infant feeding choices among Panamanian mothers: A qualitative studyDanae De La Cruz, Richard Philip Lee, Justine Gallagher
Infectious Diseases (London, England)|January 28, 2015
Does febrile neutropenia in adult oncology patients predispose to urinary tract infections or urosepsis?Burke A Cunha, Philip Lee, Ronik Sahn, et al.
Journal of Bacteriology|January 2, 2004
Phage shock protein PspA of Escherichia coli relieves saturation of protein export via the Tat pathwayMatthew P DeLisa, Philip Lee, Tracy Palmer, et al.
Stanford Law & Policy Review|December 15, 2006
Politics, health policy, and the American characterPhilip Lee, Thomas Oliver, A E Benjamin, et al.
Journal of Chemotherapy (Florence, Italy)|July 10, 2014
The safety of nitrofurantoin for the treatment of nosocomial catheter-associated bacteriuria (CAB) and cystitisBurke A Cunha, Philip Lee, Nicole Kaouris, et al.
BMC Palliative Care|July 26, 2015
Expert views on the factors enabling good end of life care for people with dementia: a qualitative studyRichard Philip Lee, Claire Bamford, Catherine Exley, et al.
Dementia (London, England)|May 29, 2016
Medical students' views about person-centred communication in dementia careEllen StClair Tullo, Tony Johnstone Young, Richard Philip Lee
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 23, 2009
Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorderCoro Paisán-Ruiz, Geoff Scopes, Philip Lee, et al.
Pageof 13

Showing results (21-30 of 128) with videos related to

Sort By:
Pageof 13
Qualitative Health Research|August 21, 2015
Talking About Looking: Three Approaches to Interviewing Carers of People With Rheumatoid Arthritis About Information SeekingRichard Philip Lee, Ben Thompson, Paul Whybrow, et al.
Biomedical Microdevices|February 24, 2006
Microfluidic alignment of collagen fibers for in vitro cell culturePhilip Lee, Rob Lin, James Moon, et al.
Food Science & Nutrition|October 12, 2023
Infant feeding choices among Panamanian mothers: A qualitative studyDanae De La Cruz, Richard Philip Lee, Justine Gallagher
Infectious Diseases (London, England)|January 28, 2015
Does febrile neutropenia in adult oncology patients predispose to urinary tract infections or urosepsis?Burke A Cunha, Philip Lee, Ronik Sahn, et al.
Journal of Bacteriology|January 2, 2004
Phage shock protein PspA of Escherichia coli relieves saturation of protein export via the Tat pathwayMatthew P DeLisa, Philip Lee, Tracy Palmer, et al.
Stanford Law & Policy Review|December 15, 2006
Politics, health policy, and the American characterPhilip Lee, Thomas Oliver, A E Benjamin, et al.
Journal of Chemotherapy (Florence, Italy)|July 10, 2014
The safety of nitrofurantoin for the treatment of nosocomial catheter-associated bacteriuria (CAB) and cystitisBurke A Cunha, Philip Lee, Nicole Kaouris, et al.
BMC Palliative Care|July 26, 2015
Expert views on the factors enabling good end of life care for people with dementia: a qualitative studyRichard Philip Lee, Claire Bamford, Catherine Exley, et al.
Dementia (London, England)|May 29, 2016
Medical students' views about person-centred communication in dementia careEllen StClair Tullo, Tony Johnstone Young, Richard Philip Lee
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 23, 2009
Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorderCoro Paisán-Ruiz, Geoff Scopes, Philip Lee, et al.
Pageof 13