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Elizabeth Stevens

Showing results (31-40 of 36) with videos related to

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World Journal of Otorhinolaryngology - Head and Neck Surgery|December 7, 2023
Postoperative mometasone irrigations improve quality of life in skull base tumor patientsMandy K Salmon, Rijul S Kshirsagar, Jacob G Eide, et al.
EMBO Reports|October 1, 2019
A new patient-derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α-dystroglycanJihee Kim, Beatrice Lana, Silvia Torelli, et al.
BMJ Open|January 14, 2025
The MyLungHealth study protocol: a pragmatic patient-randomised controlled trial to evaluate a patient-centred, electronic health record-integrated intervention to enhance lung cancer screening in primary carePolina Kukhareva, Christian Balbin, Elizabeth Stevens, et al.
Brain : a Journal of Neurology|January 5, 2013
ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophiesSebahattin Cirak, Aileen Reghan Foley, Ralf Herrmann, et al.
American Journal of Human Genetics|March 5, 2013
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanElizabeth Stevens, Keren J Carss, Sebahattin Cirak, et al.
American Journal of Human Genetics|June 18, 2013
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycanKeren J Carss, Elizabeth Stevens, A Reghan Foley, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
World Journal of Otorhinolaryngology - Head and Neck Surgery|December 7, 2023
Postoperative mometasone irrigations improve quality of life in skull base tumor patientsMandy K Salmon, Rijul S Kshirsagar, Jacob G Eide, et al.
EMBO Reports|October 1, 2019
A new patient-derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α-dystroglycanJihee Kim, Beatrice Lana, Silvia Torelli, et al.
BMJ Open|January 14, 2025
The MyLungHealth study protocol: a pragmatic patient-randomised controlled trial to evaluate a patient-centred, electronic health record-integrated intervention to enhance lung cancer screening in primary carePolina Kukhareva, Christian Balbin, Elizabeth Stevens, et al.
Brain : a Journal of Neurology|January 5, 2013
ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophiesSebahattin Cirak, Aileen Reghan Foley, Ralf Herrmann, et al.
American Journal of Human Genetics|March 5, 2013
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanElizabeth Stevens, Keren J Carss, Sebahattin Cirak, et al.
American Journal of Human Genetics|June 18, 2013
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycanKeren J Carss, Elizabeth Stevens, A Reghan Foley, et al.
Pageof 4