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 (541-550 of 565) with videos related to

Pageof 57
Sort By:
Neuromuscular Disorders : NMD|September 29, 2019
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centreEnrico Bugiardini, Alaa M Khan, Rahul Phadke, et al.
Mbio|October 23, 2025
Zoonotic <i>Escherichia coli</i> and urinary tract infections in Southern CaliforniaMaliha Aziz, Daniel E Park, Vanessa Quinlivan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 1, 2025
Transition of patients with Duchenne muscular dystrophy from paediatric to adult care: An international Delphi consensus studyDiana Castro, Thomas Sejersen, Luca Bello, et al.
Neurology|January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophyM Kinali, V Arechavala-Gomeza, S Cirak, et al.
JAMA Network Open|December 4, 2025
Triazole Resistance and Misidentification of Aspergillus tubingensis in Southern CaliforniaYashan Wang, Maliha Aziz, Kaeley Bush, et al.
Molecular Biology Reports|March 20, 2021
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial diseaseAlejandro Horga, Andreea Manole, Alice L Mitchell, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 23, 2013
Hereditary myopathy with early respiratory failure: occurrence in various populationsJohanna Palmio, Anni Evilä, Françoise Chapon, et al.
Orphanet Journal of Rare Diseases|July 24, 2023
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participationWalaa Karazi, Renata S Scalco, Mads G Stemmerik, et al.
Pageof 57

Showing results (541-550 of 565) with videos related to

Sort By:
Pageof 57
Neuromuscular Disorders : NMD|September 29, 2019
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centreEnrico Bugiardini, Alaa M Khan, Rahul Phadke, et al.
Mbio|October 23, 2025
Zoonotic <i>Escherichia coli</i> and urinary tract infections in Southern CaliforniaMaliha Aziz, Daniel E Park, Vanessa Quinlivan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 1, 2025
Transition of patients with Duchenne muscular dystrophy from paediatric to adult care: An international Delphi consensus studyDiana Castro, Thomas Sejersen, Luca Bello, et al.
Neurology|January 26, 2011
Muscle histology vs MRI in Duchenne muscular dystrophyM Kinali, V Arechavala-Gomeza, S Cirak, et al.
JAMA Network Open|December 4, 2025
Triazole Resistance and Misidentification of Aspergillus tubingensis in Southern CaliforniaYashan Wang, Maliha Aziz, Kaeley Bush, et al.
Molecular Biology Reports|March 20, 2021
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial diseaseAlejandro Horga, Andreea Manole, Alice L Mitchell, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 23, 2013
Hereditary myopathy with early respiratory failure: occurrence in various populationsJohanna Palmio, Anni Evilä, Françoise Chapon, et al.
Orphanet Journal of Rare Diseases|July 24, 2023
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participationWalaa Karazi, Renata S Scalco, Mads G Stemmerik, et al.
Pageof 57