L H Booij|A F Deutman - JoVE Visualize

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Anesthesia and Analgesia|December 1, 1989

Effects of halothane on the conduction system of the heart in humansG J Scheffer, R Jonges, H S Holley, et al.

Pharmaceutisch Weekblad. Scientific Edition|June 21, 1991

Pharmacokinetics of nicomorphine and its metabolites in man after epidural administrationP M Koopman-Kimenai, T B Vree, M A Hasenbos, et al.

Postgraduate Medical Journal|January 1, 1985

Lack of effects of emulsified propofol ('Diprivan') on vecuronium pharmacodynamics--preliminary results in manP M De Grood, J Van Egmond, M Van De Wetering, et al.

Ophthalmology|July 27, 2001

Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatusC A Driessen, B P Janssen, H J Winkens, et al.

Acta Anaesthesiologica Scandinavica|January 1, 1991

The effects of a 16-N-homopiperidino analogue of vecuronium on neuromuscular transmission in anaesthetized cats, pigs, dogs and monkeys, and in isolated preparationsA W Muir, K Anderson, R J Marshall, et al.

Ophthalmic Genetics|March 23, 2002

Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)J J C van Lith-Verhoeven, S D van der Velde-Visser, M M Sohocki, et al.

Genomics|June 22, 1999

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.

Molecular and Cellular Biology|May 29, 2000

Disruption of the 11-cis-retinol dehydrogenase gene leads to accumulation of cis-retinols and cis-retinyl estersC A Driessen, H J Winkens, K Hoffmann, et al.

Journal of Medicinal Chemistry|December 22, 2000

Non-depolarizing neuromuscular blocking activity of bisquaternary amino di- and tripeptide derivativesL H Booij, L A van der Broek, W Caulfield, et al.

Human Molecular Genetics|April 18, 1998

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRF P Cremers, D J van de Pol, M van Driel, et al.

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Showing results (181-190 of 193) with videos related to

Sort By:

Pageof 20

Anesthesia and Analgesia|December 1, 1989

Effects of halothane on the conduction system of the heart in humansG J Scheffer, R Jonges, H S Holley, et al.

Pharmaceutisch Weekblad. Scientific Edition|June 21, 1991

Pharmacokinetics of nicomorphine and its metabolites in man after epidural administrationP M Koopman-Kimenai, T B Vree, M A Hasenbos, et al.

Postgraduate Medical Journal|January 1, 1985

Lack of effects of emulsified propofol ('Diprivan') on vecuronium pharmacodynamics--preliminary results in manP M De Grood, J Van Egmond, M Van De Wetering, et al.

Ophthalmology|July 27, 2001

Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatusC A Driessen, B P Janssen, H J Winkens, et al.

Acta Anaesthesiologica Scandinavica|January 1, 1991

The effects of a 16-N-homopiperidino analogue of vecuronium on neuromuscular transmission in anaesthetized cats, pigs, dogs and monkeys, and in isolated preparationsA W Muir, K Anderson, R J Marshall, et al.

Ophthalmic Genetics|March 23, 2002

Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13)J J C van Lith-Verhoeven, S D van der Velde-Visser, M M Sohocki, et al.

Genomics|June 22, 1999

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridizationA I den Hollander, M A van Driel, Y J de Kok, et al.

Molecular and Cellular Biology|May 29, 2000

Disruption of the 11-cis-retinol dehydrogenase gene leads to accumulation of cis-retinols and cis-retinyl estersC A Driessen, H J Winkens, K Hoffmann, et al.

Journal of Medicinal Chemistry|December 22, 2000

Non-depolarizing neuromuscular blocking activity of bisquaternary amino di- and tripeptide derivativesL H Booij, L A van der Broek, W Caulfield, et al.

Human Molecular Genetics|April 18, 1998

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRF P Cremers, D J van de Pol, M van Driel, et al.

Pageof 20