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

R A Lewis

Showing results (351-360 of 381) with videos related to

Pageof 39
Sort By:
European Journal of Neurology|August 11, 2019
Patient-reported outcomes with subcutaneous immunoglobulin in chronic inflammatory demyelinating polyneuropathy: the PATH studyH-P Hartung, R Mallick, V Bril, et al.
American Journal of Medical Genetics|March 29, 1996
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)F Greenberg, R A Lewis, L Potocki, et al.
Science (New York, N.Y.)|September 20, 1997
Mutation of the Stargardt disease gene (ABCR) in age-related macular degenerationR Allikmets, N F Shroyer, N Singh, et al.
Human Mutation|October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.
Genetic Epidemiology|December 19, 2000
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancerG E Airewele, A J Sigurdson, K J Wiley, et al.
Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.
Physics in Medicine and Biology|October 21, 2005
Dynamic imaging of the lungs using x-ray phase contrastR A Lewis, N Yagi, M J Kitchen, et al.
American Journal of Human Genetics|April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1I Stoilov, A N Akarsu, I Alozie, et al.
Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.
The British Journal of Radiology|May 24, 2003
X-ray refraction effects: application to the imaging of biological tissuesR A Lewis, C J Hall, A P Hufton, et al.
Pageof 39

Showing results (351-360 of 381) with videos related to

Sort By:
Pageof 39
European Journal of Neurology|August 11, 2019
Patient-reported outcomes with subcutaneous immunoglobulin in chronic inflammatory demyelinating polyneuropathy: the PATH studyH-P Hartung, R Mallick, V Bril, et al.
American Journal of Medical Genetics|March 29, 1996
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)F Greenberg, R A Lewis, L Potocki, et al.
Science (New York, N.Y.)|September 20, 1997
Mutation of the Stargardt disease gene (ABCR) in age-related macular degenerationR Allikmets, N F Shroyer, N Singh, et al.
Human Mutation|October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.
Genetic Epidemiology|December 19, 2000
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancerG E Airewele, A J Sigurdson, K J Wiley, et al.
Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.
Physics in Medicine and Biology|October 21, 2005
Dynamic imaging of the lungs using x-ray phase contrastR A Lewis, N Yagi, M J Kitchen, et al.
American Journal of Human Genetics|April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1I Stoilov, A N Akarsu, I Alozie, et al.
Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.
The British Journal of Radiology|May 24, 2003
X-ray refraction effects: application to the imaging of biological tissuesR A Lewis, C J Hall, A P Hufton, et al.
Pageof 39