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Journal of Pediatric Genetics|February 10, 2017
Newborn Screening for Lysosomal Storage DisordersRoy W A Peake, Olaf A BodamerScientific Reports|July 9, 2020
Author Correction: Clinical Validation of Targeted and Untargeted Metabolomics Testing for Genetic Disorders: A 3 Year Comparative StudyNaif A M Almontashiri, Li Zha, Kim Young, et al.Scientific Reports|June 12, 2020
Clinical Validation of Targeted and Untargeted Metabolomics Testing for Genetic Disorders: A 3 Year Comparative StudyNaif A M Almontashiri, Li Zha, Kim Young, et al.Wiener Medizinische Wochenschrift (1946)|August 18, 2010
Laboratory and genetic evaluation of Gaucher diseaseOlaf A Bodamer, Christina HungCurrent Protocols in Human Genetics|October 18, 2012
Diagnosing lysosomal storage disorders: Pompe diseaseOlaf A Bodamer, Angela DajnokiJournal of Child Neurology|August 2, 2002
Practical management of combined methylmalonicaciduria and homocystinuriaDebra L Smith, Olaf A BodamerMolecular Genetics and Metabolism|August 17, 2014
The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): A changing landscapeOlaf A Bodamer, Roberto Giugliani, Tim WoodCurrent Protocols in Human Genetics|April 19, 2013
Diagnosing lysosomal storage disorders: Fabry diseaseOlaf A Bodamer, Britt Johnson, Angela DajnokiCurrent Protocols in Human Genetics|January 21, 2015
Diagnosing lysosomal storage disorders: mucopolysaccharidosis type IBritt A Johnson, Angela Dajnoki, Olaf A BodamerPediatrics|November 23, 2017
Newborn Screening for Pompe DiseaseOlaf A Bodamer, C Ronald Scott, Roberto Giugliani, et al.Pageof 9