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

Adam P Booth

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
BMJ (Clinical Research Ed.)|July 18, 2012
Ocular inflammation as a manifestation of Lyme borreliosisJael M Howlett, Adam P Booth
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 31, 2019
Manifestation of papilloedema secondary to intracranial hypertension following trabeculectomy in juvenile open angle glaucomaAndrew J Swampillai, Adam P Booth
Journal of Perioperative Practice|February 17, 2011
Glaucoma surgeryNeil Modi, Kaveh Vahdani, Adam P Booth
European Journal of Ophthalmology|January 21, 2017
Chorioretinal folds in a patient with multiple myeloma treated with stem cell transplantJia S Poon, Kaveh Vahdani, Adam P Booth
Journal of Glaucoma|January 25, 2020
Ciliary Body and Iris Metastases With Anterior Chamber Angle Infiltration: A Rare Complication From Invasive Ductal Breast CancerAndrew J Swampillai, Adam P Booth, Victoria M L Cohen
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 13, 2010
Genotype-phenotype correlation for leber congenital amaurosis in Northern PakistanMartin McKibbin, Manir Ali, Moin D Mohamed, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individualsAlex W Hewitt, Sonya L Bennett, Julia E Richards, et al.
Molecular Vision|July 29, 2010
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc colobomaManir Ali, Beatriz Buentello-Volante, Martin McKibbin, et al.
American Journal of Human Genetics|May 5, 2009
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in miceDavid A Parry, Carmel Toomes, Lina Bida, et al.
Human Molecular Genetics|February 8, 2017
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertilityNicola Bedoni, Lonneke Haer-Wigman, Veronika Vaclavik, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
BMJ (Clinical Research Ed.)|July 18, 2012
Ocular inflammation as a manifestation of Lyme borreliosisJael M Howlett, Adam P Booth
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|July 31, 2019
Manifestation of papilloedema secondary to intracranial hypertension following trabeculectomy in juvenile open angle glaucomaAndrew J Swampillai, Adam P Booth
Journal of Perioperative Practice|February 17, 2011
Glaucoma surgeryNeil Modi, Kaveh Vahdani, Adam P Booth
European Journal of Ophthalmology|January 21, 2017
Chorioretinal folds in a patient with multiple myeloma treated with stem cell transplantJia S Poon, Kaveh Vahdani, Adam P Booth
Journal of Glaucoma|January 25, 2020
Ciliary Body and Iris Metastases With Anterior Chamber Angle Infiltration: A Rare Complication From Invasive Ductal Breast CancerAndrew J Swampillai, Adam P Booth, Victoria M L Cohen
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 13, 2010
Genotype-phenotype correlation for leber congenital amaurosis in Northern PakistanMartin McKibbin, Manir Ali, Moin D Mohamed, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individualsAlex W Hewitt, Sonya L Bennett, Julia E Richards, et al.
Molecular Vision|July 29, 2010
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc colobomaManir Ali, Beatriz Buentello-Volante, Martin McKibbin, et al.
American Journal of Human Genetics|May 5, 2009
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in miceDavid A Parry, Carmel Toomes, Lina Bida, et al.
Human Molecular Genetics|February 8, 2017
Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertilityNicola Bedoni, Lonneke Haer-Wigman, Veronika Vaclavik, et al.
Pageof 1