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R Gatti

Showing results (211-220 of 239) with videos related to

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Clinical Genetics|July 18, 2002
An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage diseaseR Biancheri, E Verbeek, A Rossi, et al.
Communications in Agricultural and Applied Biological Sciences|March 11, 2005
Pesticides re-entry dermal exposure of workers in greenhousesV Caffarelli, E Conte, A Correnti, et al.
Journal of Medical Genetics|April 1, 1991
Aldolase B mutations in Italian families affected by hereditary fructose intoleranceG Sebastio, R de Franchis, P Strisciuglio, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletionC Bruno, C Minetti, Y Tang, et al.
Molecular Medicine (Cambridge, Mass.)|November 20, 2001
Interleukin-6 and glucocorticoids synergistically induce human immunodeficiency virus type-1 expression in chronically infected U1 cells by a long terminal repeat independent post-transcriptional mechanismA L Kinter, P Biswas, M Alfano, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Mutations among Italian mucopolysaccharidosis type I patientsR Gatti, P DiNatale, G R Villani, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 30, 2013
Predictors of effectiveness of multidisciplinary rehabilitation treatment on motor dysfunction in multiple sclerosisG Liberatore, F Clarelli, A Nuara, et al.
Cephalalgia : an International Journal of Headache|September 25, 2007
Ethanol causes neurogenic vasodilation by TRPV1 activation and CGRP release in the trigeminovascular system of the guinea pigP Nicoletti, M Trevisani, M Manconi, et al.
Genomics|January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndromeG Palmieri, V Capra, G Romano, et al.
Pageof 24

Showing results (211-220 of 239) with videos related to

Sort By:
Pageof 24
Clinical Genetics|July 18, 2002
An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage diseaseR Biancheri, E Verbeek, A Rossi, et al.
Communications in Agricultural and Applied Biological Sciences|March 11, 2005
Pesticides re-entry dermal exposure of workers in greenhousesV Caffarelli, E Conte, A Correnti, et al.
Journal of Medical Genetics|April 1, 1991
Aldolase B mutations in Italian families affected by hereditary fructose intoleranceG Sebastio, R de Franchis, P Strisciuglio, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletionC Bruno, C Minetti, Y Tang, et al.
Molecular Medicine (Cambridge, Mass.)|November 20, 2001
Interleukin-6 and glucocorticoids synergistically induce human immunodeficiency virus type-1 expression in chronically infected U1 cells by a long terminal repeat independent post-transcriptional mechanismA L Kinter, P Biswas, M Alfano, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Mutations among Italian mucopolysaccharidosis type I patientsR Gatti, P DiNatale, G R Villani, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 30, 2013
Predictors of effectiveness of multidisciplinary rehabilitation treatment on motor dysfunction in multiple sclerosisG Liberatore, F Clarelli, A Nuara, et al.
Cephalalgia : an International Journal of Headache|September 25, 2007
Ethanol causes neurogenic vasodilation by TRPV1 activation and CGRP release in the trigeminovascular system of the guinea pigP Nicoletti, M Trevisani, M Manconi, et al.
Genomics|January 1, 1992
The iduronate sulfatase gene: isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndromeG Palmieri, V Capra, G Romano, et al.
Pageof 24