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Emily Spencer

Showing results (11-20 of 32) with videos related to

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Plos One|March 28, 2025
Delivering systems-level change to improve post-diagnostic dementia support: Qualitative findings from the PriDem studyEmily Spencer, Katie Flanagan, Marie Poole, et al.
BMJ Open|July 8, 2024
Access to personalised dementia care planning in primary care: a mixed methods evaluation of the PriDem interventionEmily Spencer, Sarah Griffiths, Katie Flanagan, et al.
Biophysical Journal|February 1, 2005
Mechanisms governing the level of susceptibility of erythrocyte membranes to secretory phospholipase A2Lauren B Jensen, Nancy K Burgess, Denise D Gonda, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Identification of SPRED1 deletions using RT-PCR, multiplex ligation-dependent probe amplification and quantitative PCREmily Spencer, Julia Davis, Fady Mikhail, et al.
BMJ Open|July 13, 2024
Evaluating a model of best practice in primary care led post-diagnostic dementia care: feasibility and acceptability findings from the PriDem studySarah Griffiths, Emily Spencer, Katie Flanagan, et al.
BMJ Open|August 19, 2023
Protocol for the feasibility and implementation study of a model of best practice in primary care led postdiagnostic dementia care: PriDemSarah Griffiths, Emily Spencer, Jane Wilcock, et al.
Journal of the Air & Waste Management Association (1995)|March 7, 2022
Wintertime haze and ozone at Dinosaur National MonumentAnthony J Prenni, Katherine B Benedict, Derek E Day, et al.
NIH Consensus and State-Of-The-Science Statements|March 16, 2010
NIH consensus development conference draft statement on vaginal birth after cesarean: new insightsF Gary Cunningham, Shrikant I Bangdiwala, Sarah S Brown, et al.
American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndromeNaiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Plos One|March 28, 2025
Delivering systems-level change to improve post-diagnostic dementia support: Qualitative findings from the PriDem studyEmily Spencer, Katie Flanagan, Marie Poole, et al.
BMJ Open|July 8, 2024
Access to personalised dementia care planning in primary care: a mixed methods evaluation of the PriDem interventionEmily Spencer, Sarah Griffiths, Katie Flanagan, et al.
Biophysical Journal|February 1, 2005
Mechanisms governing the level of susceptibility of erythrocyte membranes to secretory phospholipase A2Lauren B Jensen, Nancy K Burgess, Denise D Gonda, et al.
American Journal of Medical Genetics. Part A|May 7, 2011
Identification of SPRED1 deletions using RT-PCR, multiplex ligation-dependent probe amplification and quantitative PCREmily Spencer, Julia Davis, Fady Mikhail, et al.
BMJ Open|July 13, 2024
Evaluating a model of best practice in primary care led post-diagnostic dementia care: feasibility and acceptability findings from the PriDem studySarah Griffiths, Emily Spencer, Katie Flanagan, et al.
BMJ Open|August 19, 2023
Protocol for the feasibility and implementation study of a model of best practice in primary care led postdiagnostic dementia care: PriDemSarah Griffiths, Emily Spencer, Jane Wilcock, et al.
Journal of the Air & Waste Management Association (1995)|March 7, 2022
Wintertime haze and ozone at Dinosaur National MonumentAnthony J Prenni, Katherine B Benedict, Derek E Day, et al.
NIH Consensus and State-Of-The-Science Statements|March 16, 2010
NIH consensus development conference draft statement on vaginal birth after cesarean: new insightsF Gary Cunningham, Shrikant I Bangdiwala, Sarah S Brown, et al.
American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndromeNaiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Pageof 4