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R Artuso

Showing results (1-10 of 8) with videos related to

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Chaos (Woodbury, N.Y.)|March 2, 2015
Oseledets' splitting of standard-like mapsM Sala, R Artuso
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|July 20, 2001
Asymptotic quantum behavior of classically anomalous mapsR Artuso, M Rusconi
Neuroscience|January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architectureI Meloni, V Parri, R De Filippis, et al.
Human Mutation|September 20, 2006
The Italian XLMR bank: a clinical and molecular databaseC Pescucci, R Caselli, F Mari, et al.
The Pharmacogenomics Journal|July 23, 2014
Therapeutic implications of novel mutations of the RFX6 gene associated with early-onset diabetesR Artuso, A Provenzano, B Mazzinghi, et al.
European Journal of Medical Genetics|November 8, 2006
2q24-q31 deletion: report of a case and review of the literatureC Pescucci, R Caselli, S Grosso, et al.
Brain & Development|April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteriaR Artuso, M A Mencarelli, R Polli, et al.
Journal of Medical Genetics|July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndromeM A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Chaos (Woodbury, N.Y.)|March 2, 2015
Oseledets' splitting of standard-like mapsM Sala, R Artuso
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|July 20, 2001
Asymptotic quantum behavior of classically anomalous mapsR Artuso, M Rusconi
Neuroscience|January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architectureI Meloni, V Parri, R De Filippis, et al.
Human Mutation|September 20, 2006
The Italian XLMR bank: a clinical and molecular databaseC Pescucci, R Caselli, F Mari, et al.
The Pharmacogenomics Journal|July 23, 2014
Therapeutic implications of novel mutations of the RFX6 gene associated with early-onset diabetesR Artuso, A Provenzano, B Mazzinghi, et al.
European Journal of Medical Genetics|November 8, 2006
2q24-q31 deletion: report of a case and review of the literatureC Pescucci, R Caselli, S Grosso, et al.
Brain & Development|April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteriaR Artuso, M A Mencarelli, R Polli, et al.
Journal of Medical Genetics|July 7, 2009
Novel FOXG1 mutations associated with the congenital variant of Rett syndromeM A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Pageof 1