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Wen-Chen Liang

Showing results (1-10 of 50) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|January 29, 2013
Daily or alternative, that is the question: steroid therapy for Duchenne muscular dystrophy patientsWen-Chen Liang, Ichizo Nishino
Current Neurology and Neuroscience Reports|November 4, 2010
Lipid storage myopathyWen-Chen Liang, Ichizo Nishino
Frontiers in Neurology|April 6, 2023
Pediatric immune-mediated necrotizing myopathyChen-Hua Wang, Wen-Chen Liang
The Kaohsiung Journal of Medical Sciences|July 20, 2006
Diphyllobothriasis latum: the first child case report in TaiwanHsiao-Feng Chou, Chuan-Min Yen, Wen-Chen Liang, et al.
Pediatrics and Neonatology|October 27, 2021
Combination of thrombocytopenia and hypocalcemia may indicate the possibility of Stormorken Syndrome with STIM1 mutationChen-Hua Wang, Wen-Chen Liang, Pei-Chin Lin, et al.
BMC Neurology|February 28, 2021
Exacerbation of myopathy triggered by antiobesity drugs in a patient with multiple acyl-CoA dehydrogenase deficiencyPo-Yu Lin, Wen-Chen Liang, Wei-An Liao, et al.
Pediatrics and Neonatology|April 20, 2013
Pelizaeus-Merzbacher disease, easily misdiagnosed as cerebral palsy: a report of a three-generation familyYen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 9, 2010
High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencyTze-Kiong Er, Wen-Chen Liang, Jan-Gowth Chang, et al.
Pediatrics and Neonatology|April 20, 2013
Limb-girdle muscular dystrophy type 2a with mutation in CAPN3: the first report in TaiwanChien-Hua Wang, Wen-Chen Liang, Narihiro Minami, et al.
Pediatric Neurology|January 22, 2008
Clinical and genetic features in a MELAS child with a 3271T>C mutationHsiao-Feng Chou, Wen-Chen Liang, Qing Zhang, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Journal of Neurology, Neurosurgery, and Psychiatry|January 29, 2013
Daily or alternative, that is the question: steroid therapy for Duchenne muscular dystrophy patientsWen-Chen Liang, Ichizo Nishino
Current Neurology and Neuroscience Reports|November 4, 2010
Lipid storage myopathyWen-Chen Liang, Ichizo Nishino
Frontiers in Neurology|April 6, 2023
Pediatric immune-mediated necrotizing myopathyChen-Hua Wang, Wen-Chen Liang
The Kaohsiung Journal of Medical Sciences|July 20, 2006
Diphyllobothriasis latum: the first child case report in TaiwanHsiao-Feng Chou, Chuan-Min Yen, Wen-Chen Liang, et al.
Pediatrics and Neonatology|October 27, 2021
Combination of thrombocytopenia and hypocalcemia may indicate the possibility of Stormorken Syndrome with STIM1 mutationChen-Hua Wang, Wen-Chen Liang, Pei-Chin Lin, et al.
BMC Neurology|February 28, 2021
Exacerbation of myopathy triggered by antiobesity drugs in a patient with multiple acyl-CoA dehydrogenase deficiencyPo-Yu Lin, Wen-Chen Liang, Wei-An Liao, et al.
Pediatrics and Neonatology|April 20, 2013
Pelizaeus-Merzbacher disease, easily misdiagnosed as cerebral palsy: a report of a three-generation familyYen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 9, 2010
High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencyTze-Kiong Er, Wen-Chen Liang, Jan-Gowth Chang, et al.
Pediatrics and Neonatology|April 20, 2013
Limb-girdle muscular dystrophy type 2a with mutation in CAPN3: the first report in TaiwanChien-Hua Wang, Wen-Chen Liang, Narihiro Minami, et al.
Pediatric Neurology|January 22, 2008
Clinical and genetic features in a MELAS child with a 3271T>C mutationHsiao-Feng Chou, Wen-Chen Liang, Qing Zhang, et al.
Pageof 5