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Chaos (Woodbury, N.Y.)
|
March 2, 2015
Oseledets' splitting of standard-like maps
M Sala, R Artuso
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
July 20, 2001
Asymptotic quantum behavior of classically anomalous maps
R Artuso, M Rusconi
Neuroscience
|
January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architecture
I Meloni, V Parri, R De Filippis, et al.
Human Mutation
|
September 20, 2006
The Italian XLMR bank: a clinical and molecular database
C 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 diabetes
R 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 literature
C Pescucci, R Caselli, S Grosso, et al.
Brain & Development
|
April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria
R 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 syndrome
M A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Chaos (Woodbury, N.Y.)
|
March 2, 2015
Oseledets' splitting of standard-like maps
M Sala, R Artuso
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
July 20, 2001
Asymptotic quantum behavior of classically anomalous maps
R Artuso, M Rusconi
Neuroscience
|
January 27, 2009
The XLMR gene ACSL4 plays a role in dendritic spine architecture
I Meloni, V Parri, R De Filippis, et al.
Human Mutation
|
September 20, 2006
The Italian XLMR bank: a clinical and molecular database
C 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 diabetes
R 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 literature
C Pescucci, R Caselli, S Grosso, et al.
Brain & Development
|
April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria
R 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 syndrome
M A Mencarelli, A Spanhol-Rosseto, R Artuso, et al.
Page
of 1