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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 healthcare
V Raffa, O Vittorio, C Riggio, et al.
Technology in Cancer Research & Treatment
|
April 6, 2012
BNNT-mediated irreversible electroporation: its potential on cancer cells
V 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-thalassemia
V 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 epilepsy
S 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 periodontitis
G 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 genotypes
D 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 mutations
C 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 families
A 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-q13.1
E Gennaro, M Malacarne, I Carbone, et al.
Human Molecular Genetics
|
July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsies
T Sander, H Schulz, K Saar, et al.
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of 1
Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
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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 healthcare
V Raffa, O Vittorio, C Riggio, et al.
Technology in Cancer Research & Treatment
|
April 6, 2012
BNNT-mediated irreversible electroporation: its potential on cancer cells
V 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-thalassemia
V 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 epilepsy
S 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 periodontitis
G 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 genotypes
D 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 mutations
C 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 families
A 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-q13.1
E Gennaro, M Malacarne, I Carbone, et al.
Human Molecular Genetics
|
July 11, 2000
Genome search for susceptibility loci of common idiopathic generalised epilepsies
T Sander, H Schulz, K Saar, et al.
Page
of 1