Showing results (171-180 of 193) with videos related to

Sort By:
Pageof 20
American Journal of Human Genetics|August 26, 2000
Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophyA Maugeri, B J Klevering, K Rohrschneider, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 29, 1998
A randomized controlled clinical trial on the efficacy of radiation therapy in the control of subfoveal choroidal neovascularization in age-related macular degeneration: radiation versus observationG J Bergink, C B Hoyng, R W van der Maazen, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 29, 1997
[Malignant hyperthermia as a complication of anesthesia: predisposition is hereditary]M M Snoeck, M J Gielen, R C Sengers, et al.
British Journal of Anaesthesia|July 1, 1992
Factors affecting magnitude and time course of neuromuscular block produced by suxamethoniumL E Vanlinthout, J van Egmond, T de Boo, et al.
The Journal of Pharmacy and Pharmacology|November 1, 1978
Potentiation of neostigmine and pyridostigmine by 4-aminopyridine in the ratR D Miller, P A Dennissen, F van der Pol, et al.
Neuroreport|June 7, 2000
Retinoic acid delays transcription of human retinal pigment neuroepithelium marker genes in ARPE-19 cellsJ J Janssen, E D Kuhlmann, A H van Vugt, et al.
Current Eye Research|October 16, 1999
Retinoic acid receptors and retinoid X receptors in the mature retina: subtype determination and cellular distributionJ J Janssen, E D Kuhlmann, A H van Vugt, et al.
FEBS Letters|July 8, 1998
The visual cycle retinol dehydrogenase: possible involvement in the 9-cis retinoic acid biosynthetic pathwayC A Driessen, H J Winkens, E D Kuhlmann, et al.
Gene|January 13, 1998
Cloning and structural analysis of the murine GCN5L1 geneC A Driessen, H J Winkens, L D Kuhlmann, et al.
Pageof 20