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Plos One
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March 28, 2025
Delivering systems-level change to improve post-diagnostic dementia support: Qualitative findings from the PriDem study
Emily 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 intervention
Emily Spencer, Sarah Griffiths, Katie Flanagan, et al.
Biophysical Journal
|
February 1, 2005
Mechanisms governing the level of susceptibility of erythrocyte membranes to secretory phospholipase A2
Lauren 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 PCR
Emily 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 study
Sarah 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: PriDem
Sarah 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 Monument
Anthony 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 insights
F 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 hypoplasia
Naiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
American Journal of Human Genetics
|
December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndrome
Naiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Plos One
|
March 28, 2025
Delivering systems-level change to improve post-diagnostic dementia support: Qualitative findings from the PriDem study
Emily 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 intervention
Emily Spencer, Sarah Griffiths, Katie Flanagan, et al.
Biophysical Journal
|
February 1, 2005
Mechanisms governing the level of susceptibility of erythrocyte membranes to secretory phospholipase A2
Lauren 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 PCR
Emily 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 study
Sarah 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: PriDem
Sarah 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 Monument
Anthony 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 insights
F 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 hypoplasia
Naiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
American Journal of Human Genetics
|
December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndrome
Naiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Page
of 4