Search research articles
Contact Us
Filters
Showing results (41-50 of 57) with videos related to
Page
of 6
Sort By:
International Journal of Molecular Sciences
|
June 12, 2026
Heterozygous Nonsense Mutation in the Nuclear Transport Factor <i>KPNA7</i>, a Maternal Factor Active in Embryonic Tissues, Causes Autosomal Dominant Otosclerosis
Tammy Benteau, Nelly Abdelfatah, Anne Griffin, et al.
Advances in Chronic Kidney Disease
|
March 13, 2008
Community-partnered approaches to enhance chronic kidney disease awareness, prevention, and early intervention
Roberto B Vargas, Loretta Jones, Chrystene Terry, et al.
Nursing Administration Quarterly
|
March 7, 2017
Progress on a Call to Action: Nurses as Leaders in Disaster Preparedness and Response
Mary Pat Couig, Alicia Gable, Anne Griffin, et al.
International Journal of Audiology
|
October 6, 2021
"Something is just not right with my hearing": early experiences of adults living with hearing loss
April Pike, Sheila Moodie, Karen Parsons, et al.
Journal of Nursing Scholarship : an Official Publication of Sigma Theta Tau International Honor Society of Nursing
|
February 13, 2016
Nurses as Leaders in Disaster Preparedness and Response--A Call to Action
Tener Goodwin Veenema, Anne Griffin, Alicia R Gable, et al.
Pilot and Feasibility Studies
|
January 4, 2022
A physiotherapy-led transition to home intervention for older adults following emergency department discharge: protocol for a pilot feasibility randomised controlled trial
Mairéad Conneely, Aoife Leahy, Margaret O'Connor, et al.
BMC Medical Genetics
|
May 4, 2019
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss
Justin A Pater, Jane Green, Darren D O'Rielly, et al.
European Journal of Human Genetics : EJHG
|
February 28, 2013
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL
Nelly Abdelfatah, David A McComiskey, Lance Doucette, et al.
Human Genetics
|
November 14, 2016
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect
Justin A Pater, Tammy Benteau, Anne Griffin, et al.
Journal of General Internal Medicine
|
January 10, 2008
Programmable infusion pumps in ICUs: an analysis of corresponding adverse drug events
Teryl K Nuckols, Anthony G Bower, Susan M Paddock, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 57) with videos related to
Sort By:
Page
of 6
International Journal of Molecular Sciences
|
June 12, 2026
Heterozygous Nonsense Mutation in the Nuclear Transport Factor <i>KPNA7</i>, a Maternal Factor Active in Embryonic Tissues, Causes Autosomal Dominant Otosclerosis
Tammy Benteau, Nelly Abdelfatah, Anne Griffin, et al.
Advances in Chronic Kidney Disease
|
March 13, 2008
Community-partnered approaches to enhance chronic kidney disease awareness, prevention, and early intervention
Roberto B Vargas, Loretta Jones, Chrystene Terry, et al.
Nursing Administration Quarterly
|
March 7, 2017
Progress on a Call to Action: Nurses as Leaders in Disaster Preparedness and Response
Mary Pat Couig, Alicia Gable, Anne Griffin, et al.
International Journal of Audiology
|
October 6, 2021
"Something is just not right with my hearing": early experiences of adults living with hearing loss
April Pike, Sheila Moodie, Karen Parsons, et al.
Journal of Nursing Scholarship : an Official Publication of Sigma Theta Tau International Honor Society of Nursing
|
February 13, 2016
Nurses as Leaders in Disaster Preparedness and Response--A Call to Action
Tener Goodwin Veenema, Anne Griffin, Alicia R Gable, et al.
Pilot and Feasibility Studies
|
January 4, 2022
A physiotherapy-led transition to home intervention for older adults following emergency department discharge: protocol for a pilot feasibility randomised controlled trial
Mairéad Conneely, Aoife Leahy, Margaret O'Connor, et al.
BMC Medical Genetics
|
May 4, 2019
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss
Justin A Pater, Jane Green, Darren D O'Rielly, et al.
European Journal of Human Genetics : EJHG
|
February 28, 2013
Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL
Nelly Abdelfatah, David A McComiskey, Lance Doucette, et al.
Human Genetics
|
November 14, 2016
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect
Justin A Pater, Tammy Benteau, Anne Griffin, et al.
Journal of General Internal Medicine
|
January 10, 2008
Programmable infusion pumps in ICUs: an analysis of corresponding adverse drug events
Teryl K Nuckols, Anthony G Bower, Susan M Paddock, et al.
Page
of 6