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 Kaiser-Kupfer

Showing results (11-20 of 25) with videos related to

Pageof 3
Sort By:
Arthritis and Rheumatism|March 1, 1981
Successful treatment of sudden hearing loss in Cogan's syndrome with corticosteroidsB F Haynes, A Pikus, M Kaiser-Kupfer, et al.
Retina (Philadelphia, Pa.)|February 24, 2001
A case of Alport's syndrome and retinal degenerationE Tsilou, B I Rubin, R C Caruso, et al.
Vision Research|January 1, 1981
Studies using human lenses from a family displaying hereditary congenital cataractsP Russell, S Uga, J S Zigler, et al.
Molecular Genetics and Metabolism|October 27, 1998
Identification, isolation, and characterization of a 32-kDa fatty acid-binding protein missing from lymphocytes in humans with Bietti crystalline dystrophy (BCD)J Lee, X Jiao, J F Hejtmancik, et al.
Human Genetics|October 1, 1996
Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysisD Stone, Y Ning, X Y Guan, et al.
Molecular Vision|October 27, 1998
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin geneC Kannabiran, P K Rogan, L Olmos, et al.
American Journal of Human Genetics|October 1, 1995
Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12T Padma, R Ayyagari, J S Murty, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
The metabolism of fatty acids in human Bietti crystalline dystrophyJ Lee, X Jiao, J F Hejtmancik, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1984
Cellular and humoral immune parameters among patients with retinitis pigmentosa and other retinal disordersD Benezra, I Gery, C C Chan, et al.
The Journal of Clinical Investigation|February 1, 1988
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retinaG A Mitchell, L C Brody, J Looney, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Arthritis and Rheumatism|March 1, 1981
Successful treatment of sudden hearing loss in Cogan's syndrome with corticosteroidsB F Haynes, A Pikus, M Kaiser-Kupfer, et al.
Retina (Philadelphia, Pa.)|February 24, 2001
A case of Alport's syndrome and retinal degenerationE Tsilou, B I Rubin, R C Caruso, et al.
Vision Research|January 1, 1981
Studies using human lenses from a family displaying hereditary congenital cataractsP Russell, S Uga, J S Zigler, et al.
Molecular Genetics and Metabolism|October 27, 1998
Identification, isolation, and characterization of a 32-kDa fatty acid-binding protein missing from lymphocytes in humans with Bietti crystalline dystrophy (BCD)J Lee, X Jiao, J F Hejtmancik, et al.
Human Genetics|October 1, 1996
Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysisD Stone, Y Ning, X Y Guan, et al.
Molecular Vision|October 27, 1998
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin geneC Kannabiran, P K Rogan, L Olmos, et al.
American Journal of Human Genetics|October 1, 1995
Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12T Padma, R Ayyagari, J S Murty, et al.
Investigative Ophthalmology & Visual Science|June 30, 2001
The metabolism of fatty acids in human Bietti crystalline dystrophyJ Lee, X Jiao, J F Hejtmancik, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1984
Cellular and humoral immune parameters among patients with retinitis pigmentosa and other retinal disordersD Benezra, I Gery, C C Chan, et al.
The Journal of Clinical Investigation|February 1, 1988
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retinaG A Mitchell, L C Brody, J Looney, et al.
Pageof 3