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C Riggio

Showing results (1-10 of 10) with videos related to

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Minimally Invasive Therapy & Allied Technologies : MITAT : Official Journal of the Society for Minimally Invasive Therapy|May 26, 2010
Progress in nanotechnology for healthcareV Raffa, O Vittorio, C Riggio, et al.
Technology in Cancer Research & Treatment|April 6, 2012
BNNT-mediated irreversible electroporation: its potential on cancer cellsV Raffa, C Riggio, M W Smith, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemiaV Pietrini, M Godani, S Calzetti, et al.
Journal of Medical Genetics|September 5, 2006
Novel NHLRC1 mutations and genotype-phenotype correlations in patients with Lafora's progressive myoclonic epilepsyS Singh, I Sethi, S Francheschetti, et al.
International Journal of Immunopathology and Pharmacology|October 13, 2012
Sub-micrometric liposomes as drug delivery systems in the treatment of periodontitisG Di Turi, C Riggio, O Vittorio, et al.
Journal of Neurology|July 10, 1999
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypesD Pareyson, C Gellera, B Castellotti, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutationsC Gellera, B Castellotti, M C Riggio, et al.
European Neurology|July 15, 2000
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian familiesA Filla, C Mariotti, G Caruso, 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.
Human Molecular Genetics|July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsiesT Sander, H Schulz, K Saar, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Minimally Invasive Therapy & Allied Technologies : MITAT : Official Journal of the Society for Minimally Invasive Therapy|May 26, 2010
Progress in nanotechnology for healthcareV Raffa, O Vittorio, C Riggio, et al.
Technology in Cancer Research & Treatment|April 6, 2012
BNNT-mediated irreversible electroporation: its potential on cancer cellsV Raffa, C Riggio, M W Smith, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemiaV Pietrini, M Godani, S Calzetti, et al.
Journal of Medical Genetics|September 5, 2006
Novel NHLRC1 mutations and genotype-phenotype correlations in patients with Lafora's progressive myoclonic epilepsyS Singh, I Sethi, S Francheschetti, et al.
International Journal of Immunopathology and Pharmacology|October 13, 2012
Sub-micrometric liposomes as drug delivery systems in the treatment of periodontitisG Di Turi, C Riggio, O Vittorio, et al.
Journal of Neurology|July 10, 1999
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypesD Pareyson, C Gellera, B Castellotti, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutationsC Gellera, B Castellotti, M C Riggio, et al.
European Neurology|July 15, 2000
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian familiesA Filla, C Mariotti, G Caruso, 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.
Human Molecular Genetics|July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsiesT Sander, H Schulz, K Saar, et al.
Pageof 1