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Showing results (41-50 of 59) with videos related to

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Talanta|December 6, 2014
Mercury fractionation in dourada (Brachyplatystoma rousseauxii) of the Madeira River in Brazil using metalloproteomic strategiesC P Braga, A C Bittarello, C C F Padilha, et al.
Neurology|March 29, 2007
Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsH Lohi, J Turnbull, X C Zhao, et al.
Neurology|April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaI Carbone, C Bruno, F Sotgia, et al.
Neuropediatrics|July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisN Cannelli, N Nardocci, D Cassandrini, et al.
Biological Trace Element Research|May 27, 2017
Metalloproteomics Approach to Analyze Mercury in Breast Milk and Hair Samples of Lactating Women in Communities of the Amazon Basin, BrazilM R Cerbino, José Cavalcante Souza Vieira, C P Braga, et al.
Biochemical and Biophysical Research Communications|September 4, 2013
Novel FAM126A mutations in hypomyelination and congenital cataract diseaseM Traverso, S Assereto, E Gazzerro, et al.
Archives of Environmental Contamination and Toxicology|May 19, 2015
Determination of the Mercury Fraction Linked to Protein of Muscle and Liver Tissue of Tucunaré (Cichla spp.) from the Amazon Region of BrazilJosé C S Vieira, Bruna Cavecci, João V Queiroz, et al.
Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.
Epilepsia|December 28, 1999
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1E Gennaro, M Malacarne, I Carbone, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Talanta|December 6, 2014
Mercury fractionation in dourada (Brachyplatystoma rousseauxii) of the Madeira River in Brazil using metalloproteomic strategiesC P Braga, A C Bittarello, C C F Padilha, et al.
Neurology|March 29, 2007
Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsH Lohi, J Turnbull, X C Zhao, et al.
Neurology|April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaI Carbone, C Bruno, F Sotgia, et al.
Neuropediatrics|July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisN Cannelli, N Nardocci, D Cassandrini, et al.
Biological Trace Element Research|May 27, 2017
Metalloproteomics Approach to Analyze Mercury in Breast Milk and Hair Samples of Lactating Women in Communities of the Amazon Basin, BrazilM R Cerbino, José Cavalcante Souza Vieira, C P Braga, et al.
Biochemical and Biophysical Research Communications|September 4, 2013
Novel FAM126A mutations in hypomyelination and congenital cataract diseaseM Traverso, S Assereto, E Gazzerro, et al.
Archives of Environmental Contamination and Toxicology|May 19, 2015
Determination of the Mercury Fraction Linked to Protein of Muscle and Liver Tissue of Tucunaré (Cichla spp.) from the Amazon Region of BrazilJosé C S Vieira, Bruna Cavecci, João V Queiroz, et al.
Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.
Epilepsia|December 28, 1999
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1E Gennaro, M Malacarne, I Carbone, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Pageof 6