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Biochemical and Biophysical Research Communications|September 25, 1995
Galactose stabilizes various missense mutants of alpha-galactosidase in Fabry diseaseT Okumiya, S Ishii, T Takenaka, et al.Clinical Chemistry|July 17, 1998
Sensitive enzymatic assay for erythrocyte creatine with production of methylene blueT Okumiya, Y Jiao, T Saibara, et al.Expert Opinion on Medical Diagnostics|March 19, 2013
Enzymatic and molecular strategies to diagnose Pompe diseaseAjj Reuser, Fw Verheijen, Ma Kroos, et al.Internal Medicine (Tokyo, Japan)|May 1, 1997
High incidence of thrombosis in Fabry's diseaseK Utsumi, N Yamamoto, R Kase, et al.Clinical Biochemistry|June 12, 1998
An enzymatic assay for erythrocyte creatine as an index of the erythrocyte life timeY Jiao, T Okumiya, T Saibara, et al.Brain & Development|March 1, 1997
Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysisT Takata, T Okumiya, H Hayashibe, et al.Glycoconjugate Journal|January 9, 1999
Alpha-galactosidase transgenic mouse: heterogeneous gene expression and posttranslational glycosylation in tissuesS Ishii, R Kase, H Sakuraba, et al.Journal of Clinical Apheresis|January 1, 1990
Assessment of bilirubin clearance capacity of a newly developed ion-exchange adsorption column and its possible use as a supportive therapy in hepatorenal syndromeJ Sone, T Saibara, H Himeno, et al.Pageof 2