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The Lancet. Child & Adolescent Health
|
September 1, 2018
Neurological manifestations of lysosomal disorders and emerging therapies targeting the CNS
Roberto Giugliani, Filippo Vairo, Francyne Kubaski, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
A Case of Early Infantile Pompe Disease with Atypical Manifestation
Carolina F M de Souza, Karina Donnis, Filippo Vairo, et al.
Toxicon : Official Journal of the International Society on Toxinology
|
August 13, 2009
Urinary oligosaccharides: a peripheral marker for Sida carpinifolia exposure or poisoning
Marisete Bedin, Edson M Colodel, Roberto Giugliani, et al.
Journal of Inherited Metabolic Disease
|
September 18, 2012
Retroviral-vector-mediated gene therapy to mucopolysaccharidosis I mice improves sensorimotor impairments and other behavioral deficits
Guilherme Baldo, David F Wozniak, Kevin K Ohlemiller, et al.
Journal of Inherited Metabolic Disease
|
February 5, 2017
Losartan improves aortic dilatation and cardiovascular disease in mucopolysaccharidosis I
Esteban Alberto Gonzalez, Angela Maria Vicente Tavares, Edina Poletto, et al.
Current Pharmaceutical Design
|
November 3, 2020
Therapeutic Options for Mucopolysaccharidosis II (Hunter Disease)
Francyne Kubaski, Filippo Vairo, Guilherme Baldo, et al.
Molecular Genetics and Metabolism
|
December 19, 2008
New GLB1 mutation in siblings with Morquio type B disease presenting with mental regression
Fabiana Quoos Mayer, Fernanda dos Santos Pereira, Anthony H Fensom, et al.
Molecular Genetics and Metabolism
|
August 15, 2020
Safety of intrathecal delivery of recombinant human arylsulfatase A in children with metachromatic leukodystrophy: Results from a phase 1/2 clinical trial
Christine Í Dali, Caroline Sevin, Ingeborg Krägeloh-Mann, et al.
Asian Pacific Journal of Tropical Biomedicine
|
April 10, 2013
Glucose-6-phosphate-dehydrogenase deficiency and its correlation with other risk factors in jaundiced newborns in Southern Brazil
Clarissa Gutiérrez Carvalho, Simone Martins Castro, Ana Paula Santin, et al.
Plos One
|
February 4, 2015
Effects of enzyme replacement therapy started late in a murine model of mucopolysaccharidosis type I
Gabriela Pasqualim, Guilherme Baldo, Talita Giacomet de Carvalho, et al.
Page
of 49
Search research articles
Search
Showing results (91-100 of 482) with videos related to
Sort By:
Page
of 49
The Lancet. Child & Adolescent Health
|
September 1, 2018
Neurological manifestations of lysosomal disorders and emerging therapies targeting the CNS
Roberto Giugliani, Filippo Vairo, Francyne Kubaski, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
A Case of Early Infantile Pompe Disease with Atypical Manifestation
Carolina F M de Souza, Karina Donnis, Filippo Vairo, et al.
Toxicon : Official Journal of the International Society on Toxinology
|
August 13, 2009
Urinary oligosaccharides: a peripheral marker for Sida carpinifolia exposure or poisoning
Marisete Bedin, Edson M Colodel, Roberto Giugliani, et al.
Journal of Inherited Metabolic Disease
|
September 18, 2012
Retroviral-vector-mediated gene therapy to mucopolysaccharidosis I mice improves sensorimotor impairments and other behavioral deficits
Guilherme Baldo, David F Wozniak, Kevin K Ohlemiller, et al.
Journal of Inherited Metabolic Disease
|
February 5, 2017
Losartan improves aortic dilatation and cardiovascular disease in mucopolysaccharidosis I
Esteban Alberto Gonzalez, Angela Maria Vicente Tavares, Edina Poletto, et al.
Current Pharmaceutical Design
|
November 3, 2020
Therapeutic Options for Mucopolysaccharidosis II (Hunter Disease)
Francyne Kubaski, Filippo Vairo, Guilherme Baldo, et al.
Molecular Genetics and Metabolism
|
December 19, 2008
New GLB1 mutation in siblings with Morquio type B disease presenting with mental regression
Fabiana Quoos Mayer, Fernanda dos Santos Pereira, Anthony H Fensom, et al.
Molecular Genetics and Metabolism
|
August 15, 2020
Safety of intrathecal delivery of recombinant human arylsulfatase A in children with metachromatic leukodystrophy: Results from a phase 1/2 clinical trial
Christine Í Dali, Caroline Sevin, Ingeborg Krägeloh-Mann, et al.
Asian Pacific Journal of Tropical Biomedicine
|
April 10, 2013
Glucose-6-phosphate-dehydrogenase deficiency and its correlation with other risk factors in jaundiced newborns in Southern Brazil
Clarissa Gutiérrez Carvalho, Simone Martins Castro, Ana Paula Santin, et al.
Plos One
|
February 4, 2015
Effects of enzyme replacement therapy started late in a murine model of mucopolysaccharidosis type I
Gabriela Pasqualim, Guilherme Baldo, Talita Giacomet de Carvalho, et al.
Page
of 49