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W L Hwu

Showing results (71-80 of 77) with videos related to

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Molecular Genetics and Metabolism|August 7, 2009
Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort studyM Pineda, J E Wraith, E Mengel, et al.
European Journal of Neurology|May 29, 2009
A longitudinal study of Taiwanese sialidosis type 1: an insight into the concept of cherry-red spot myoclonus syndromeS-C Lai, R-S Chen, Y-H Wu Chou, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 18, 2011
Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesisY-S Yang, G-C Ma, J-C Shih, et al.
Molecular Genetics and Metabolism|March 13, 2012
Expert recommendations for the laboratory diagnosis of MPS VIT Wood, O A Bodamer, M G Burin, et al.
European Neurology|July 27, 2004
DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patientsC K Wang, Y R Wu, W L Hwu, et al.
Neurology|May 28, 2010
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiencyL Brun, L H Ngu, W T Keng, et al.
Neurology|December 8, 2006
Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe diseaseP S Kishnani, D Corzo, M Nicolino, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Molecular Genetics and Metabolism|August 7, 2009
Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort studyM Pineda, J E Wraith, E Mengel, et al.
European Journal of Neurology|May 29, 2009
A longitudinal study of Taiwanese sialidosis type 1: an insight into the concept of cherry-red spot myoclonus syndromeS-C Lai, R-S Chen, Y-H Wu Chou, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 18, 2011
Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesisY-S Yang, G-C Ma, J-C Shih, et al.
Molecular Genetics and Metabolism|March 13, 2012
Expert recommendations for the laboratory diagnosis of MPS VIT Wood, O A Bodamer, M G Burin, et al.
European Neurology|July 27, 2004
DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patientsC K Wang, Y R Wu, W L Hwu, et al.
Neurology|May 28, 2010
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiencyL Brun, L H Ngu, W T Keng, et al.
Neurology|December 8, 2006
Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe diseaseP S Kishnani, D Corzo, M Nicolino, et al.
Pageof 8