Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Roberto Giugliani

Showing results (181-190 of 482) with videos related to

Pageof 49
Sort By:
Jornal De Pediatria|August 17, 2006
Prospective study of 11 Brazilian patients with mucopolysaccharidosis IILouise L C Pinto, Ida V D Schwartz, Ana C S Puga, et al.
Genetics and Molecular Biology|April 24, 2020
Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancerEdenir Inêz Palmero, Natalia Campacci, Lavinia Schüler-Faccini, et al.
Digestive Diseases and Sciences|April 17, 2010
Bone marrow mononuclear cell transplantation improves survival and induces hepatocyte proliferation in rats after CCl(4) acute liver damageGuilherme Baldo, Roberto Giugliani, Carolina Uribe, et al.
Arquivos Brasileiros De Cardiologia|October 14, 2016
Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional StudyBeatriz Piva E Mattos, Fernando Luís Scolari, Marco Antonio Rodrigues Torres, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysisMichael Beck, Derralynn Hughes, Christoph Kampmann, et al.
Orphanet Journal of Rare Diseases|May 11, 2021
Prospective study of the natural history of chronic acid sphingomyelinase deficiency in children and adults: eleven years of observationMargaret M McGovern, Melissa P Wasserstein, Bruno Bembi, et al.
Molecular Genetics and Metabolism|May 22, 2018
Glycosaminoglycans analysis in blood and urine of patients with mucopolysaccharidosisShaukat A Khan, Robert W Mason, Roberto Giugliani, et al.
Acta Dermato-Venereologica|May 2, 2006
Dermal melanocytosis associated with GM1-gangliosidosis type 1Leila David Bloch, Fernando Yoshiaki Matsumoto, Walter Belda, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 26, 2005
Biochemical properties of beta-glucosidase in leukocytes from patients and obligated heterozygotes for Gaucher disease carriersKristiane Michelin, Alessandro Wajner, Hugo Bock, et al.
Molecular Genetics and Metabolism|December 27, 2014
Shotgun proteomics reveals possible mechanisms for cognitive impairment in Mucopolysaccharidosis I miceGuilherme Baldo, Daniel Macedo Lorenzini, Diogenes Santiago Santos, et al.
Pageof 49

Showing results (181-190 of 482) with videos related to

Sort By:
Pageof 49
Jornal De Pediatria|August 17, 2006
Prospective study of 11 Brazilian patients with mucopolysaccharidosis IILouise L C Pinto, Ida V D Schwartz, Ana C S Puga, et al.
Genetics and Molecular Biology|April 24, 2020
Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancerEdenir Inêz Palmero, Natalia Campacci, Lavinia Schüler-Faccini, et al.
Digestive Diseases and Sciences|April 17, 2010
Bone marrow mononuclear cell transplantation improves survival and induces hepatocyte proliferation in rats after CCl(4) acute liver damageGuilherme Baldo, Roberto Giugliani, Carolina Uribe, et al.
Arquivos Brasileiros De Cardiologia|October 14, 2016
Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional StudyBeatriz Piva E Mattos, Fernando Luís Scolari, Marco Antonio Rodrigues Torres, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysisMichael Beck, Derralynn Hughes, Christoph Kampmann, et al.
Orphanet Journal of Rare Diseases|May 11, 2021
Prospective study of the natural history of chronic acid sphingomyelinase deficiency in children and adults: eleven years of observationMargaret M McGovern, Melissa P Wasserstein, Bruno Bembi, et al.
Molecular Genetics and Metabolism|May 22, 2018
Glycosaminoglycans analysis in blood and urine of patients with mucopolysaccharidosisShaukat A Khan, Robert W Mason, Roberto Giugliani, et al.
Acta Dermato-Venereologica|May 2, 2006
Dermal melanocytosis associated with GM1-gangliosidosis type 1Leila David Bloch, Fernando Yoshiaki Matsumoto, Walter Belda, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 26, 2005
Biochemical properties of beta-glucosidase in leukocytes from patients and obligated heterozygotes for Gaucher disease carriersKristiane Michelin, Alessandro Wajner, Hugo Bock, et al.
Molecular Genetics and Metabolism|December 27, 2014
Shotgun proteomics reveals possible mechanisms for cognitive impairment in Mucopolysaccharidosis I miceGuilherme Baldo, Daniel Macedo Lorenzini, Diogenes Santiago Santos, et al.
Pageof 49