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Archivos Argentinos De Pediatria
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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 neuroscience
Luca Corradi, Gabriele Arnulfo, Andrea Schenone, et al.
European Journal of Rheumatology
|
February 3, 2017
When arthralgia is not arthritis
Juan 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 decisions
Ivan Porro, Andrea Schenone, Marco Fato, et al.
Neuroinformatics
|
January 8, 2011
Grid-distributed statistical parametric mapping of SPECT and PET neuroimages
Isabella Castiglioni, Barbara Canesi, Andrea Schenone, et al.
BMC Bioinformatics
|
April 14, 2007
A Grid-based solution for management and analysis of microarrays in distributed experiments
Ivan 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 management
Luisa 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 neuroscience
Luca 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 mutation
Stefania Zampieri, Annalisa Montalvo, Mariana Blanco, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 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 neuroscience
Luca Corradi, Gabriele Arnulfo, Andrea Schenone, et al.
European Journal of Rheumatology
|
February 3, 2017
When arthralgia is not arthritis
Juan 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 decisions
Ivan Porro, Andrea Schenone, Marco Fato, et al.
Neuroinformatics
|
January 8, 2011
Grid-distributed statistical parametric mapping of SPECT and PET neuroimages
Isabella Castiglioni, Barbara Canesi, Andrea Schenone, et al.
BMC Bioinformatics
|
April 14, 2007
A Grid-based solution for management and analysis of microarrays in distributed experiments
Ivan 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 management
Luisa 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 neuroscience
Luca 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 mutation
Stefania Zampieri, Annalisa Montalvo, Mariana Blanco, et al.
Page
of 2