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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
January 19, 2012
Newborn screening for Pompe disease: an update, 2011
Barbara K Burton
European Journal of Pediatrics
|
March 3, 2012
Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfalls
Barbara K Burton, Roberto Giugliani
Molecular Genetics and Metabolism
|
November 3, 2007
Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II
Brad Angle, Barbara K Burton
American Journal of Medical Genetics. Part A
|
June 9, 2012
Survey of health status and complications among propionic acidemia patients
Loren Pena, Barbara K Burton
Molecular Genetics and Metabolism
|
July 20, 2010
Reaching out to the lost generation of adults with early-treated phenylketonuria (PKU)
Barbara K Burton, Lauren Leviton
Molecular Genetics and Metabolism
|
November 19, 2013
Increased incidence of neonatal respiratory distress in infants with mucopolysaccharidosis type II (MPS II, Hunter syndrome)
Charlotte Dodsworth, Barbara K Burton
Touchreviews in Endocrinology
|
February 4, 2022
Diagnosis and Clinical Management of Long-chain Fatty-acid Oxidation Disorders: A Review
Joshua J Baker, Barbara K Burton
Current Medical Research and Opinion
|
March 22, 2017
Progression of liver disease in children and adults with lysosomal acid lipase deficiency
Barbara K Burton, Nancy Silliman, Sachin Marulkar
Molecular Genetics and Metabolism
|
March 29, 2011
Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)
Barbara K Burton, David A H Whiteman,
International Journal of Neonatal Screening
|
October 29, 2020
Newborn Screening for Mucopolysaccharidosis Type II in Illinois: An Update
Barbara K Burton, Rachel Hickey, Lauren Hitchins
Page
of 13
Search research articles
Search
Showing results (1-10 of 122) with videos related to
Sort By:
Page
of 13
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
January 19, 2012
Newborn screening for Pompe disease: an update, 2011
Barbara K Burton
European Journal of Pediatrics
|
March 3, 2012
Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfalls
Barbara K Burton, Roberto Giugliani
Molecular Genetics and Metabolism
|
November 3, 2007
Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II
Brad Angle, Barbara K Burton
American Journal of Medical Genetics. Part A
|
June 9, 2012
Survey of health status and complications among propionic acidemia patients
Loren Pena, Barbara K Burton
Molecular Genetics and Metabolism
|
July 20, 2010
Reaching out to the lost generation of adults with early-treated phenylketonuria (PKU)
Barbara K Burton, Lauren Leviton
Molecular Genetics and Metabolism
|
November 19, 2013
Increased incidence of neonatal respiratory distress in infants with mucopolysaccharidosis type II (MPS II, Hunter syndrome)
Charlotte Dodsworth, Barbara K Burton
Touchreviews in Endocrinology
|
February 4, 2022
Diagnosis and Clinical Management of Long-chain Fatty-acid Oxidation Disorders: A Review
Joshua J Baker, Barbara K Burton
Current Medical Research and Opinion
|
March 22, 2017
Progression of liver disease in children and adults with lysosomal acid lipase deficiency
Barbara K Burton, Nancy Silliman, Sachin Marulkar
Molecular Genetics and Metabolism
|
March 29, 2011
Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)
Barbara K Burton, David A H Whiteman,
International Journal of Neonatal Screening
|
October 29, 2020
Newborn Screening for Mucopolysaccharidosis Type II in Illinois: An Update
Barbara K Burton, Rachel Hickey, Lauren Hitchins
Page
of 13