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

Quinlivan

Showing results (411-420 of 565) with videos related to

Pageof 57
Sort By:
Plos One|June 21, 2013
Hypomethylation of serum blood clot DNA, but not plasma EDTA-blood cell pellet DNA, from vitamin B12-deficient subjectsEoin P Quinlivan, Krista S Crider, Jiang-Hui Zhu, et al.
Journal of Neuromuscular Diseases|March 1, 2021
Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment EraMaggie C Walter, Claudia Chiriboga, Tina Duong, et al.
Neuromuscular Disorders : NMD|February 10, 2018
GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2)Mahalekshmi Desikan, Renata Siciliani Scalco, Andreea Manole, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 11, 2002
Folate synthesis in plants: the first step of the pterin branch is mediated by a unique bimodular GTP cyclohydrolase IGilles Basset, Eoin P Quinlivan, Michael J Ziemak, et al.
European Journal of Nuclear Medicine and Molecular Imaging|April 13, 2011
Evaluation of [¹²³I]-CLINDE as a potent SPECT radiotracer to assess the degree of astroglia activation in cuprizone-induced neuroinflammationFilomena Mattner, David Linares Bandin, Maria Staykova, et al.
Neuromuscular Disorders : NMD|July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle diseaseSacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Bjpsych Open|September 8, 2025
Umbrella review of psychosocial and ward-based interventions to reduce self-harm and suicide risks in in-patient mental health settingsLeah Quinlivan, Jodie Westhead, Jane Graney, et al.
BMJ Open|October 22, 2024
Care gaps among people presenting to the hospital following self-harm: observational study of three emergency departments in EnglandSarah Steeg, Harriet Bickley, Caroline Clements, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 24, 2010
McArdle disease: a clinical reviewR Quinlivan, J Buckley, M James, et al.
Archives of Neurology|May 19, 2004
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variantEugenio Mercuri, Maja Poppe, Ros Quinlivan, et al.
Pageof 57

Showing results (411-420 of 565) with videos related to

Sort By:
Pageof 57
Plos One|June 21, 2013
Hypomethylation of serum blood clot DNA, but not plasma EDTA-blood cell pellet DNA, from vitamin B12-deficient subjectsEoin P Quinlivan, Krista S Crider, Jiang-Hui Zhu, et al.
Journal of Neuromuscular Diseases|March 1, 2021
Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment EraMaggie C Walter, Claudia Chiriboga, Tina Duong, et al.
Neuromuscular Disorders : NMD|February 10, 2018
GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2)Mahalekshmi Desikan, Renata Siciliani Scalco, Andreea Manole, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 11, 2002
Folate synthesis in plants: the first step of the pterin branch is mediated by a unique bimodular GTP cyclohydrolase IGilles Basset, Eoin P Quinlivan, Michael J Ziemak, et al.
European Journal of Nuclear Medicine and Molecular Imaging|April 13, 2011
Evaluation of [¹²³I]-CLINDE as a potent SPECT radiotracer to assess the degree of astroglia activation in cuprizone-induced neuroinflammationFilomena Mattner, David Linares Bandin, Maria Staykova, et al.
Neuromuscular Disorders : NMD|July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle diseaseSacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Bjpsych Open|September 8, 2025
Umbrella review of psychosocial and ward-based interventions to reduce self-harm and suicide risks in in-patient mental health settingsLeah Quinlivan, Jodie Westhead, Jane Graney, et al.
BMJ Open|October 22, 2024
Care gaps among people presenting to the hospital following self-harm: observational study of three emergency departments in EnglandSarah Steeg, Harriet Bickley, Caroline Clements, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 24, 2010
McArdle disease: a clinical reviewR Quinlivan, J Buckley, M James, et al.
Archives of Neurology|May 19, 2004
Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variantEugenio Mercuri, Maja Poppe, Ros Quinlivan, et al.
Pageof 57