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Journal of Inherited Metabolic Disease|October 13, 2001
A common 2 bp deletion mutation in the glucose-6-phosphatase gene in Indian patients with glycogen storage disease type IaC Meaney, T Cranston, P Lee, et al.Journal of Inherited Metabolic Disease|December 16, 2000
Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutationsS Genet, T Cranston, H R Middleton-PriceMedicine and Science in Sports and Exercise|November 14, 1998
The effect of exercise training on the severity and duration of a viral upper respiratory illnessT G Weidner, T Cranston, T Schurr, et al.Experimental Brain Research|July 9, 2017
Decreased spontaneous activity and altered evoked nociceptive response of rat thalamic submedius neurons to lumbar vertebra thrustWilliam R Reed, Jamie T Cranston, Stephen M Onifer, et al.Blood|July 27, 2001
Defective expression of the interleukin-2/interleukin-15 receptor beta subunit leads to a natural killer cell-deficient form of severe combined immunodeficiencyK C Gilmour, H Fujii, T Cranston, et al.BMC Psychiatry|October 2, 2024
A randomized controlled trial of a self-guided mobile app targeting repetitive negative thought to prevent depression in university students: study protocol of the Nurture-U Reducing Worry prevention trialE R Watkins, D Phillips, T Cranston, et al.Human Mutation|October 23, 2001
Eleven novel JAK3 mutations in patients with severe combined immunodeficiency-including the first patients with mutations in the kinase domainP Mella, R F Schumacher, T Cranston, et al.Journal of Inherited Metabolic Disease|May 26, 2004
How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?S Grünewald, L Fairbanks, S Genet, et al.Clinical and Experimental Immunology|October 27, 2001
X-linked lymphoproliferative disease: three atypical casesK Nistala, K C Gilmour, T Cranston, et al.Pageof 2