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Roberto Giugliani

Showing results (11-20 of 482) with videos related to

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Expert Opinion on Drug Delivery|January 24, 2014
Gene delivery strategies for the treatment of mucopolysaccharidosesGuilherme Baldo, Roberto Giugliani, Ursula Matte
JIMD Reports|January 8, 2024
Characterization of orthopedic manifestations in patients with mucopolysaccharidosis II using data from 15 years of the Hunter Outcome SurveyBianca Link, Jaco Botha, Roberto Giugliani
Expert Opinion on Investigational Drugs|October 26, 2017
Phase I and II clinical trials for the mucopolysaccharidosesFabiano Poswar, Guilherme Baldo, Roberto Giugliani
Community Genetics|April 1, 2008
Consumption of folic acid-fortified flour and folate-rich foods among women at reproductive age in South BrazilAna Flávia S Ferreira, Roberto Giugliani
Medical Hypotheses|February 25, 2014
Lysosomal enzymes may cross the blood-brain-barrier by pinocytosis: implications for enzyme replacement therapyGuilherme Baldo, Roberto Giugliani, Ursula Matte
Journal of Community Genetics|June 30, 2025
Community genetics in Brazil- a 2025 perspectiveRoberto Giugliani, Dafne Dain Gandelman Horovitz
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2004
Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern BrazilTêmis Maria Félix, Sandra Leistner, Roberto Giugliani
Molecular Genetics and Metabolism|August 17, 2014
The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): A changing landscapeOlaf A Bodamer, Roberto Giugliani, Tim Wood
Pediatrics|August 3, 2007
Management guidelines for mucopolysaccharidosis VIRoberto Giugliani, Paul Harmatz, James E Wraith
Pediatrics|November 23, 2017
Newborn Screening for Pompe DiseaseOlaf A Bodamer, C Ronald Scott, Roberto Giugliani, et al.
Pageof 49

Showing results (11-20 of 482) with videos related to

Sort By:
Pageof 49
Expert Opinion on Drug Delivery|January 24, 2014
Gene delivery strategies for the treatment of mucopolysaccharidosesGuilherme Baldo, Roberto Giugliani, Ursula Matte
JIMD Reports|January 8, 2024
Characterization of orthopedic manifestations in patients with mucopolysaccharidosis II using data from 15 years of the Hunter Outcome SurveyBianca Link, Jaco Botha, Roberto Giugliani
Expert Opinion on Investigational Drugs|October 26, 2017
Phase I and II clinical trials for the mucopolysaccharidosesFabiano Poswar, Guilherme Baldo, Roberto Giugliani
Community Genetics|April 1, 2008
Consumption of folic acid-fortified flour and folate-rich foods among women at reproductive age in South BrazilAna Flávia S Ferreira, Roberto Giugliani
Medical Hypotheses|February 25, 2014
Lysosomal enzymes may cross the blood-brain-barrier by pinocytosis: implications for enzyme replacement therapyGuilherme Baldo, Roberto Giugliani, Ursula Matte
Journal of Community Genetics|June 30, 2025
Community genetics in Brazil- a 2025 perspectiveRoberto Giugliani, Dafne Dain Gandelman Horovitz
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2004
Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern BrazilTêmis Maria Félix, Sandra Leistner, Roberto Giugliani
Molecular Genetics and Metabolism|August 17, 2014
The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): A changing landscapeOlaf A Bodamer, Roberto Giugliani, Tim Wood
Pediatrics|August 3, 2007
Management guidelines for mucopolysaccharidosis VIRoberto Giugliani, Paul Harmatz, James E Wraith
Pediatrics|November 23, 2017
Newborn Screening for Pompe DiseaseOlaf A Bodamer, C Ronald Scott, Roberto Giugliani, et al.
Pageof 49