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P J Morrison

Showing results (121-130 of 155) with videos related to

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European Journal of Clinical Pharmacology|January 1, 1981
Plasma and salivary pharmacokinetics of caffeine in manR Newton, L J Broughton, M J Lind, et al.
Biopharmaceutics & Drug Disposition|January 1, 1982
Bioavailability of phenylbutazone from a new enteric-coated formulation with superior dissolution characteristicsV A John, S Goldsborough, P J Morrison, et al.
British Journal of Clinical Pharmacology|April 1, 1986
Comparison of pharmacokinetic profiles of single and multiple doses of a slow release Oros oxprenolol delivery system in young normotensive and elderly hypertensive subjectsI D Bradbrook, M Babiker, P Crome, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2000
Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenitaN P Davies, L H Eunson, R P Gregory, et al.
The Journal of Antimicrobial Chemotherapy|May 1, 1983
Pharmacokinetics and bioavailability of sultamicillin estimated by high performance liquid chromatographyH J ROgers, I D Bradbrook, P J Morrison, et al.
Mucosal Immunology|March 7, 2013
Th17-cell plasticity in Helicobacter hepaticus-induced intestinal inflammationP J Morrison, D Bending, L A Fouser, et al.
Clinical and Experimental Dermatology|August 3, 2021
Development and preliminary evaluation of the Neurofibromatosis Type 1 Adult Quality of Life (NF1-AdQoL) questionnaireH Crawford, K North, M J Wilson, et al.
Clinical Genetics|June 18, 2015
Uptake of health monitoring and disease self-management in Australian adults with neurofibromatosis type 1: strategies to improve careH A Crawford, B Barton, M J Wilson, et al.
Neurology|November 30, 2006
Levetiracetam in pregnancy: preliminary experience from the UK Epilepsy and Pregnancy RegisterS Hunt, J Craig, A Russell, et al.
Journal of Medical Genetics|December 1, 1993
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary choreaJ C MacMillan, P J Morrison, N C Nevin, et al.
Pageof 16

Showing results (121-130 of 155) with videos related to

Sort By:
Pageof 16
European Journal of Clinical Pharmacology|January 1, 1981
Plasma and salivary pharmacokinetics of caffeine in manR Newton, L J Broughton, M J Lind, et al.
Biopharmaceutics & Drug Disposition|January 1, 1982
Bioavailability of phenylbutazone from a new enteric-coated formulation with superior dissolution characteristicsV A John, S Goldsborough, P J Morrison, et al.
British Journal of Clinical Pharmacology|April 1, 1986
Comparison of pharmacokinetic profiles of single and multiple doses of a slow release Oros oxprenolol delivery system in young normotensive and elderly hypertensive subjectsI D Bradbrook, M Babiker, P Crome, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2000
Clinical, electrophysiological, and molecular genetic studies in a new family with paramyotonia congenitaN P Davies, L H Eunson, R P Gregory, et al.
The Journal of Antimicrobial Chemotherapy|May 1, 1983
Pharmacokinetics and bioavailability of sultamicillin estimated by high performance liquid chromatographyH J ROgers, I D Bradbrook, P J Morrison, et al.
Mucosal Immunology|March 7, 2013
Th17-cell plasticity in Helicobacter hepaticus-induced intestinal inflammationP J Morrison, D Bending, L A Fouser, et al.
Clinical and Experimental Dermatology|August 3, 2021
Development and preliminary evaluation of the Neurofibromatosis Type 1 Adult Quality of Life (NF1-AdQoL) questionnaireH Crawford, K North, M J Wilson, et al.
Clinical Genetics|June 18, 2015
Uptake of health monitoring and disease self-management in Australian adults with neurofibromatosis type 1: strategies to improve careH A Crawford, B Barton, M J Wilson, et al.
Neurology|November 30, 2006
Levetiracetam in pregnancy: preliminary experience from the UK Epilepsy and Pregnancy RegisterS Hunt, J Craig, A Russell, et al.
Journal of Medical Genetics|December 1, 1993
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary choreaJ C MacMillan, P J Morrison, N C Nevin, et al.
Pageof 16