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J P Lin

Showing results (91-100 of 118) with videos related to

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Journal of Biomedical Materials Research. Part B, Applied Biomaterials|November 13, 2012
Microstructure, mechanical property, corrosion behavior, and in vitro biocompatibility of Zr-Mo alloysF Y Zhou, B L Wang, K J Qiu, et al.
Developmental Medicine and Child Neurology|April 18, 2001
Safety profile and efficacy of botulinum toxin A (Dysport) in children with muscle spasticityA M Bakheit, S Severa, A Cosgrove, et al.
Developmental Medicine and Child Neurology|December 1, 1994
Low birthweight: a 10-year outcome study of the continuum of reproductive casualtyJ O Forfar, R Hume, F M McPhail, et al.
European Journal of Neurology|February 11, 2017
Efficacy of pallidal stimulation in isolated dystonia: a systematic review and meta-analysisE Moro, C LeReun, J K Krauss, et al.
Arthritis and Rheumatism|March 20, 1998
Familial autoimmunity in pedigrees of idiopathic inflammatory myopathy patients suggests common genetic risk factors for many autoimmune diseasesL R Ginn, J P Lin, P H Plotz, et al.
The Journal of Clinical Investigation|July 4, 2001
Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenitaS Brownlow, R Webster, R Croxen, et al.
Radiology|July 1, 1976
Evaluation of sellar and parasellar masses by computed tomographyT P Naidich, R S Pinto, M J Kushner, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|June 17, 2005
Berberine inhibits arylamine N-acetyltransferase activity and gene expression in mouse leukemia L 1210 cellsS S Lin, J G Chung, J P Lin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 6, 2016
Differences in globus pallidus neuronal firing rates and patterns relate to different disease biology in children with dystoniaV M McClelland, A Valentin, H G Rey, et al.
Journal of Medical Genetics|November 10, 2000
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)A R Lafferty, D J Torpy, M Stowasser, et al.
Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:
Pageof 12
Journal of Biomedical Materials Research. Part B, Applied Biomaterials|November 13, 2012
Microstructure, mechanical property, corrosion behavior, and in vitro biocompatibility of Zr-Mo alloysF Y Zhou, B L Wang, K J Qiu, et al.
Developmental Medicine and Child Neurology|April 18, 2001
Safety profile and efficacy of botulinum toxin A (Dysport) in children with muscle spasticityA M Bakheit, S Severa, A Cosgrove, et al.
Developmental Medicine and Child Neurology|December 1, 1994
Low birthweight: a 10-year outcome study of the continuum of reproductive casualtyJ O Forfar, R Hume, F M McPhail, et al.
European Journal of Neurology|February 11, 2017
Efficacy of pallidal stimulation in isolated dystonia: a systematic review and meta-analysisE Moro, C LeReun, J K Krauss, et al.
Arthritis and Rheumatism|March 20, 1998
Familial autoimmunity in pedigrees of idiopathic inflammatory myopathy patients suggests common genetic risk factors for many autoimmune diseasesL R Ginn, J P Lin, P H Plotz, et al.
The Journal of Clinical Investigation|July 4, 2001
Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenitaS Brownlow, R Webster, R Croxen, et al.
Radiology|July 1, 1976
Evaluation of sellar and parasellar masses by computed tomographyT P Naidich, R S Pinto, M J Kushner, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|June 17, 2005
Berberine inhibits arylamine N-acetyltransferase activity and gene expression in mouse leukemia L 1210 cellsS S Lin, J G Chung, J P Lin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 6, 2016
Differences in globus pallidus neuronal firing rates and patterns relate to different disease biology in children with dystoniaV M McClelland, A Valentin, H G Rey, et al.
Journal of Medical Genetics|November 10, 2000
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)A R Lafferty, D J Torpy, M Stowasser, et al.
Pageof 12