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

M Michaelides

Showing results (61-70 of 98) with videos related to

Pageof 10
Sort By:
The Laryngoscope|September 28, 2002
Round window gentamicin absorption: an in vivo human modelZoran Becvarovski, Dennis I Bojrab, Elias M Michaelides, et al.
Clinical Genetics|May 11, 2016
Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health ServiceK N Khan, R Chana, N Ali, et al.
Eye (London, England)|December 16, 2017
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British familyV Berry, N Pontikos, A Moore, et al.
The American Surgeon|March 1, 1986
A phase I/II SECSG (Southeastern Cancer Study Group) pilot study of surgical adjuvant immunotherapy with vaccinia melanoma oncolysates (VMO)M K Wallack, K McNally, M Michaelides, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|February 9, 2021
Outcomes in Revision Stapes SurgeryZachary G Schwam, Amy Schettino, Seilesh C Babu, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 25, 2021
Evolving Role of Non-Total Resection in Management of Acoustic Neuroma in the Gamma Knife EraAlexander L Luryi, John F Kveton, Seilesh Babu, et al.
The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.
Folia Biologica|March 21, 2021
Phenotype Variability in Czech Patients Carrying PAX6 Disease-Causing VariantsJ Moravikova, Z Kozmik, L Hlavata, et al.
The Journal of Experimental Medicine|December 1, 1979
B6.C-H-2bm12. A new H-2 mutation in the I region in the mouseI F McKenzie, G M Morgan, M S Sandrin, et al.
Thescientificworldjournal|November 19, 2014
Hemifacial spasm and neurovascular compressionAlex Y Lu, Jacky T Yeung, Jason L Gerrard, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
The Laryngoscope|September 28, 2002
Round window gentamicin absorption: an in vivo human modelZoran Becvarovski, Dennis I Bojrab, Elias M Michaelides, et al.
Clinical Genetics|May 11, 2016
Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health ServiceK N Khan, R Chana, N Ali, et al.
Eye (London, England)|December 16, 2017
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British familyV Berry, N Pontikos, A Moore, et al.
The American Surgeon|March 1, 1986
A phase I/II SECSG (Southeastern Cancer Study Group) pilot study of surgical adjuvant immunotherapy with vaccinia melanoma oncolysates (VMO)M K Wallack, K McNally, M Michaelides, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|February 9, 2021
Outcomes in Revision Stapes SurgeryZachary G Schwam, Amy Schettino, Seilesh C Babu, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 25, 2021
Evolving Role of Non-Total Resection in Management of Acoustic Neuroma in the Gamma Knife EraAlexander L Luryi, John F Kveton, Seilesh Babu, et al.
The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.
Folia Biologica|March 21, 2021
Phenotype Variability in Czech Patients Carrying PAX6 Disease-Causing VariantsJ Moravikova, Z Kozmik, L Hlavata, et al.
The Journal of Experimental Medicine|December 1, 1979
B6.C-H-2bm12. A new H-2 mutation in the I region in the mouseI F McKenzie, G M Morgan, M S Sandrin, et al.
Thescientificworldjournal|November 19, 2014
Hemifacial spasm and neurovascular compressionAlex Y Lu, Jacky T Yeung, Jason L Gerrard, et al.
Pageof 10