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Current Protocols in Human Genetics|October 18, 2012
Diagnosing lysosomal storage disorders: Pompe diseaseOlaf A Bodamer, Angela DajnokiCurrent Protocols in Human Genetics|April 19, 2013
Diagnosing lysosomal storage disorders: Fabry diseaseOlaf A Bodamer, Britt Johnson, Angela DajnokiCurrent Protocols in Human Genetics|July 22, 2014
Diagnosis of lysosomal storage disorders: Gaucher diseaseBritt A Johnson, Angela Dajnoki, Olaf BodamerCurrent Protocols in Human Genetics|January 21, 2015
Diagnosing lysosomal storage disorders: mucopolysaccharidosis type IBritt A Johnson, Angela Dajnoki, Olaf A BodamerCurrent Protocols in Human Genetics|February 11, 2014
Diagnosing lysosomal storage disorders: mucopolysaccharidosis type IIBritt A Johnson, Otto P van Diggelen, Angela Dajnoki, et al.Annals of Laboratory Medicine|September 6, 2012
Analysis of acid sphingomyelinase activity in dried blood spots using tandem mass spectrometryElisa Legnini, Joe J Orsini, Adolf Mühl, et al.Annals of Laboratory Medicine|July 5, 2013
Analysis of lyso-globotriaosylsphingosine in dried blood spotsBritt Johnson, Hermann Mascher, Daniel Mascher, et al.Experimental Neurology|July 17, 2018
Injury type-dependent differentiation of NG2 glia into heterogeneous astrocytesAmber R Hackett, Stephanie L Yahn, Kirill Lyapichev, et al.Pageof 1