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Andrea Schenone

Showing results (1-10 of 16) with videos related to

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Archivos Argentinos De Pediatria|May 28, 2014
[Mucopolysaccharidosis type VI: clinical aspects, diagnosis and treatment with enzyme replacement therapy]Juan Politei, Andrea Schenone, Mariana Blanco, et al.
Studies in Health Technology and Informatics|July 14, 2009
XTENS - an eXTensible environment for neuroscienceLuca Corradi, Gabriele Arnulfo, Andrea Schenone, et al.
European Journal of Rheumatology|February 3, 2017
When arthralgia is not arthritisJuan Politei, Graciela Remondino, Ricardo Heguilen, et al.
Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society|May 17, 2005
An integrated environment for plastic surgery support: building virtual patients, simulating interventions, and supporting intraoperative decisionsIvan Porro, Andrea Schenone, Marco Fato, et al.
Neuroinformatics|January 8, 2011
Grid-distributed statistical parametric mapping of SPECT and PET neuroimagesIsabella Castiglioni, Barbara Canesi, Andrea Schenone, et al.
BMC Bioinformatics|April 14, 2007
A Grid-based solution for management and analysis of microarrays in distributed experimentsIvan Porro, Livia Torterolo, Luca Corradi, et al.
Archivos Argentinos De Pediatria|August 4, 2012
[Long chain 3-hydroxyacyl-coA dehydrogenase deficiency, association with HELLP and magnetic resonance spectroscopy findings]Noelia Deltetto, Clarisa Maxit, Delfina Marchione, et al.
Archivos Argentinos De Pediatria|July 25, 2019
Infantile-onset Pompe disease: Diagnosis and managementLuisa B Bay, Inés Denzler, Consuelo Durand, et al.
BMC Medical Informatics and Decision Making|October 10, 2012
A repository based on a dynamically extensible data model supporting multidisciplinary research in neuroscienceLuca Corradi, Ivan Porro, Andrea Schenone, et al.
Gene|March 24, 2012
Molecular analysis of HEXA gene in Argentinean patients affected with Tay-Sachs disease: possible common origin of the prevalent c.459+5A>G mutationStefania Zampieri, Annalisa Montalvo, Mariana Blanco, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Archivos Argentinos De Pediatria|May 28, 2014
[Mucopolysaccharidosis type VI: clinical aspects, diagnosis and treatment with enzyme replacement therapy]Juan Politei, Andrea Schenone, Mariana Blanco, et al.
Studies in Health Technology and Informatics|July 14, 2009
XTENS - an eXTensible environment for neuroscienceLuca Corradi, Gabriele Arnulfo, Andrea Schenone, et al.
European Journal of Rheumatology|February 3, 2017
When arthralgia is not arthritisJuan Politei, Graciela Remondino, Ricardo Heguilen, et al.
Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society|May 17, 2005
An integrated environment for plastic surgery support: building virtual patients, simulating interventions, and supporting intraoperative decisionsIvan Porro, Andrea Schenone, Marco Fato, et al.
Neuroinformatics|January 8, 2011
Grid-distributed statistical parametric mapping of SPECT and PET neuroimagesIsabella Castiglioni, Barbara Canesi, Andrea Schenone, et al.
BMC Bioinformatics|April 14, 2007
A Grid-based solution for management and analysis of microarrays in distributed experimentsIvan Porro, Livia Torterolo, Luca Corradi, et al.
Archivos Argentinos De Pediatria|August 4, 2012
[Long chain 3-hydroxyacyl-coA dehydrogenase deficiency, association with HELLP and magnetic resonance spectroscopy findings]Noelia Deltetto, Clarisa Maxit, Delfina Marchione, et al.
Archivos Argentinos De Pediatria|July 25, 2019
Infantile-onset Pompe disease: Diagnosis and managementLuisa B Bay, Inés Denzler, Consuelo Durand, et al.
BMC Medical Informatics and Decision Making|October 10, 2012
A repository based on a dynamically extensible data model supporting multidisciplinary research in neuroscienceLuca Corradi, Ivan Porro, Andrea Schenone, et al.
Gene|March 24, 2012
Molecular analysis of HEXA gene in Argentinean patients affected with Tay-Sachs disease: possible common origin of the prevalent c.459+5A>G mutationStefania Zampieri, Annalisa Montalvo, Mariana Blanco, et al.
Pageof 2