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

L Fraser

Showing results (601-610 of 610) with videos related to

Pageof 61
Sort By:
You have reached the last page of results.This site can display upto 610 results.
The Journal of Urology|April 17, 2012
Randomized multicenter clinical trial of myofascial physical therapy in women with interstitial cystitis/painful bladder syndrome and pelvic floor tendernessM P FitzGerald, C K Payne, E S Lukacz, et al.
Journal for Immunotherapy of Cancer|April 8, 2025
Consensus disease definitions for ophthalmic immune-related adverse events of immune checkpoint inhibitorsEileen L Chang, Renee Liu, Kiandokht Keyhanian, et al.
Molecular Genetics and Metabolism|July 4, 2024
Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophyLaura Ann Adang, Samuel Groeschel, Chloe Grzyb, et al.
Critical Care Medicine|August 17, 2018
Clinical Practice Guidelines for the Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICUJohn W Devlin, Yoanna Skrobik, Céline Gélinas, et al.
American Journal of Human Genetics|July 22, 2020
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial DysmorphismMaria J Guillen Sacoto, Iva A Tchasovnikarova, Erin Torti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2020
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
The Lancet. Neurology|September 30, 2022
Diagnosis and classification of optic neuritisAxel Petzold, Clare L Fraser, Mathias Abegg, et al.
Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disordersYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature|July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndromeYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
International Journal of Transgender Health|October 14, 2022
Standards of Care for the Health of Transgender and Gender Diverse People, Version 8E Coleman, A E Radix, W P Bouman, et al.
Pageof 61

Showing results (601-610 of 610) with videos related to

Sort By:
Pageof 61
You have reached the last page of results.This site can display upto 610 results.
The Journal of Urology|April 17, 2012
Randomized multicenter clinical trial of myofascial physical therapy in women with interstitial cystitis/painful bladder syndrome and pelvic floor tendernessM P FitzGerald, C K Payne, E S Lukacz, et al.
Journal for Immunotherapy of Cancer|April 8, 2025
Consensus disease definitions for ophthalmic immune-related adverse events of immune checkpoint inhibitorsEileen L Chang, Renee Liu, Kiandokht Keyhanian, et al.
Molecular Genetics and Metabolism|July 4, 2024
Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophyLaura Ann Adang, Samuel Groeschel, Chloe Grzyb, et al.
Critical Care Medicine|August 17, 2018
Clinical Practice Guidelines for the Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICUJohn W Devlin, Yoanna Skrobik, Céline Gélinas, et al.
American Journal of Human Genetics|July 22, 2020
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial DysmorphismMaria J Guillen Sacoto, Iva A Tchasovnikarova, Erin Torti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2020
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
The Lancet. Neurology|September 30, 2022
Diagnosis and classification of optic neuritisAxel Petzold, Clare L Fraser, Mathias Abegg, et al.
Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disordersYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature|July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndromeYuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
International Journal of Transgender Health|October 14, 2022
Standards of Care for the Health of Transgender and Gender Diverse People, Version 8E Coleman, A E Radix, W P Bouman, et al.
Pageof 61