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Roberto Giugliani

Showing results (101-110 of 482) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|June 21, 2011
Practical and reliable enzyme test for the detection of mucopolysaccharidosis IVA (Morquio Syndrome type A) in dried blood samplesMarli V Camelier, Maira G Burin, Jurema De Mari, et al.
Molecular Genetics and Metabolism Reports|November 22, 2017
Long-term outcomes with agalsidase alfa enzyme replacement therapy: Analysis using deconstructed composite eventsMichael Beck, Derralynn Hughes, Christoph Kampmann, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 21, 2003
S100B protein and amniotic fluidAdriano B L Tort, Carlos A Gonçalves, Diogo O Souza, et al.
Clinical Biochemistry|December 20, 2007
Maple syrup urine disease in treated patients: biochemical and oxidative stress profilesAlethéa G Barschak, Christiane Marchesan, Angela Sitta, et al.
Clinical Dysmorphology|April 3, 2009
Punctate calcifications in lysosomal storage disordersIda Vanessa Doederlein Schwartz, Osvaldo Artigalás, Markus Ries, et al.
Artificial Organs|July 17, 2010
Effects of cryopreservation and hypothermic storage on cell viability and enzyme activity in recombinant encapsulated cells overexpressing alpha-L-iduronidaseFabiana Quoos Mayer, Guilherme Baldo, Talita Giacomet de Carvalho, et al.
JIMD Reports|February 23, 2013
Novel mutations in the glucocerebrosidase gene of brazilian patients with Gaucher diseaseMarina Siebert, Hugo Bock, Kristiane Michelin-Tirelli, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|November 11, 2017
Gene editing of MPS I human fibroblasts by co-delivery of a CRISPR/Cas9 plasmid and a donor oligonucleotide using nanoemulsions as nonviral carriersRoselena Silvestri Schuh, Talita Giacomet de Carvalho, Roberto Giugliani, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 23, 2006
Twelve different enzyme assays on dried-blood filter paper samples for detection of patients with selected inherited lysosomal storage diseasesGabriel Civallero, Kristiane Michelin, Jurema de Mari, et al.
Molecular Genetics and Metabolism|May 6, 2011
Response of women with Fabry disease to enzyme replacement therapy: comparison with men, using data from FOS--the Fabry Outcome SurveyDerralynn A Hughes, Miguel-Ángel Barba Romero, Carla E M Hollak, et al.
Pageof 49

Showing results (101-110 of 482) with videos related to

Sort By:
Pageof 49
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 21, 2011
Practical and reliable enzyme test for the detection of mucopolysaccharidosis IVA (Morquio Syndrome type A) in dried blood samplesMarli V Camelier, Maira G Burin, Jurema De Mari, et al.
Molecular Genetics and Metabolism Reports|November 22, 2017
Long-term outcomes with agalsidase alfa enzyme replacement therapy: Analysis using deconstructed composite eventsMichael Beck, Derralynn Hughes, Christoph Kampmann, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 21, 2003
S100B protein and amniotic fluidAdriano B L Tort, Carlos A Gonçalves, Diogo O Souza, et al.
Clinical Biochemistry|December 20, 2007
Maple syrup urine disease in treated patients: biochemical and oxidative stress profilesAlethéa G Barschak, Christiane Marchesan, Angela Sitta, et al.
Clinical Dysmorphology|April 3, 2009
Punctate calcifications in lysosomal storage disordersIda Vanessa Doederlein Schwartz, Osvaldo Artigalás, Markus Ries, et al.
Artificial Organs|July 17, 2010
Effects of cryopreservation and hypothermic storage on cell viability and enzyme activity in recombinant encapsulated cells overexpressing alpha-L-iduronidaseFabiana Quoos Mayer, Guilherme Baldo, Talita Giacomet de Carvalho, et al.
JIMD Reports|February 23, 2013
Novel mutations in the glucocerebrosidase gene of brazilian patients with Gaucher diseaseMarina Siebert, Hugo Bock, Kristiane Michelin-Tirelli, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|November 11, 2017
Gene editing of MPS I human fibroblasts by co-delivery of a CRISPR/Cas9 plasmid and a donor oligonucleotide using nanoemulsions as nonviral carriersRoselena Silvestri Schuh, Talita Giacomet de Carvalho, Roberto Giugliani, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 23, 2006
Twelve different enzyme assays on dried-blood filter paper samples for detection of patients with selected inherited lysosomal storage diseasesGabriel Civallero, Kristiane Michelin, Jurema de Mari, et al.
Molecular Genetics and Metabolism|May 6, 2011
Response of women with Fabry disease to enzyme replacement therapy: comparison with men, using data from FOS--the Fabry Outcome SurveyDerralynn A Hughes, Miguel-Ángel Barba Romero, Carla E M Hollak, et al.
Pageof 49