Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Susan Maxwell

Showing results (1-10 of 46) with videos related to

Pageof 5
Sort By:
The Journal of Nursing Administration|September 16, 2004
The NEAT Project: Nursing Engineering Ambassador TeamSusan Maxwell, Robert Burns
Nursing for Women'S Health|August 21, 2012
Creating the Joint Commission "super user": an innovative plan to ensure survey readinessJean Salera-Vieira, Susan Maxwell
The Journal of Ambulatory Care Management|July 15, 2003
Building an award-winning women's health ambulatory service and beyondLisa W Allen, Susan Maxwell, John F Greene
Human Molecular Genetics|October 9, 2004
A mouse model of AChR deficiency syndrome with a phenotype reflecting the human conditionJudy Cossins, Richard Webster, Susan Maxwell, et al.
Obstetrics and Gynecology|May 10, 2017
Pregnancy Outcomes After Fertility Preservation in Transgender MenSusan Maxwell, Nicole Noyes, David Keefe, et al.
Neuromuscular Disorders : NMD|April 18, 2013
Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1Keivan Basiri, Katsiaryna Belaya, Wei Wei Liu, et al.
Mededpublish (2016)|February 26, 2024
Twelve Tips to implement Curriculum Changes in times of Economic AusterityKay Cartwright, Paladugu Madhavi, Keiarash Kazemi-Jovestani, et al.
Brain : a Journal of Neurology|March 3, 2012
A novel congenital myasthenic syndrome due to decreased acetylcholine receptor ion-channel conductanceRichard Webster, Susan Maxwell, Hayley Spearman, et al.
Annals of the New York Academy of Sciences|January 3, 2013
Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndromeKatsiaryna Belaya, Sarah Finlayson, Judith Cossins, et al.
Annals of the New York Academy of Sciences|January 25, 2018
Myasthenic syndromes due to defects in COL13A1 and in the N-linked glycosylation pathwayDavid Beeson, Judith Cossins, Pedro M Rodriguez Cruz, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
The Journal of Nursing Administration|September 16, 2004
The NEAT Project: Nursing Engineering Ambassador TeamSusan Maxwell, Robert Burns
Nursing for Women'S Health|August 21, 2012
Creating the Joint Commission "super user": an innovative plan to ensure survey readinessJean Salera-Vieira, Susan Maxwell
The Journal of Ambulatory Care Management|July 15, 2003
Building an award-winning women's health ambulatory service and beyondLisa W Allen, Susan Maxwell, John F Greene
Human Molecular Genetics|October 9, 2004
A mouse model of AChR deficiency syndrome with a phenotype reflecting the human conditionJudy Cossins, Richard Webster, Susan Maxwell, et al.
Obstetrics and Gynecology|May 10, 2017
Pregnancy Outcomes After Fertility Preservation in Transgender MenSusan Maxwell, Nicole Noyes, David Keefe, et al.
Neuromuscular Disorders : NMD|April 18, 2013
Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1Keivan Basiri, Katsiaryna Belaya, Wei Wei Liu, et al.
Mededpublish (2016)|February 26, 2024
Twelve Tips to implement Curriculum Changes in times of Economic AusterityKay Cartwright, Paladugu Madhavi, Keiarash Kazemi-Jovestani, et al.
Brain : a Journal of Neurology|March 3, 2012
A novel congenital myasthenic syndrome due to decreased acetylcholine receptor ion-channel conductanceRichard Webster, Susan Maxwell, Hayley Spearman, et al.
Annals of the New York Academy of Sciences|January 3, 2013
Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndromeKatsiaryna Belaya, Sarah Finlayson, Judith Cossins, et al.
Annals of the New York Academy of Sciences|January 25, 2018
Myasthenic syndromes due to defects in COL13A1 and in the N-linked glycosylation pathwayDavid Beeson, Judith Cossins, Pedro M Rodriguez Cruz, et al.
Pageof 5