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Christina Liang

Showing results (11-20 of 34) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 3, 2013
Axonal excitability in X-linked dominant Charcot Marie Tooth diseaseChristina Liang, James Howells, Marina Kennerson, et al.
Muscle & Nerve|May 25, 2011
Axonal hyperpolarization in inclusion-body myopathy, Paget disease of the bone, and frontotemporal dementia (IBMPFD)Kishore R Kumar, Christina Liang, Merilee Needham, et al.
Neurology|October 22, 2013
Fibroblast growth factor 21 is a sensitive biomarker of mitochondrial diseaseRyan L Davis, Christina Liang, Fabienne Edema-Hildebrand, et al.
International Journal of Rheumatic Diseases|February 4, 2025
Case Report: Inflammatory Myositis Presenting as Dropped Head Syndrome in a Patient With Rheumatoid AntibodiesEstelle Noonan, Matthew Verheyden, Hwei Choo Soh, et al.
Muscle & Nerve|September 8, 2017
Sarcolemmal excitability in the myotonic dystrophiesRobert Boland-Freitas, James Lee, James Howells, et al.
International Journal of Cardiology|December 26, 2014
Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathyPeter Kabunga, Antony K Lau, Kevin Phan, et al.
Journal of Neurology|July 2, 2013
Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegiaKishore R Kumar, Nicholas F Blair, Himesha Vandebona, et al.
Neuromuscular Disorders : NMD|August 10, 2022
A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centreWui-Kwan Wong, Samantha J Bryen, Adam Bournazos, et al.
HGG Advances|July 18, 2022
Prevalence, parameters, and pathogenic mechanisms for splice-altering acceptor variants that disrupt the AG exclusion zoneSamantha J Bryen, Michaela Yuen, Himanshu Joshi, et al.
The Lancet Regional Health. Western Pacific|November 19, 2024
A contemporary analysis of the Australian clinical and genetic landscape of spinal muscular atrophy: a registry based studyLakshmi Balaji, Robin Forbes, Anita Cairns, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 3, 2013
Axonal excitability in X-linked dominant Charcot Marie Tooth diseaseChristina Liang, James Howells, Marina Kennerson, et al.
Muscle & Nerve|May 25, 2011
Axonal hyperpolarization in inclusion-body myopathy, Paget disease of the bone, and frontotemporal dementia (IBMPFD)Kishore R Kumar, Christina Liang, Merilee Needham, et al.
Neurology|October 22, 2013
Fibroblast growth factor 21 is a sensitive biomarker of mitochondrial diseaseRyan L Davis, Christina Liang, Fabienne Edema-Hildebrand, et al.
International Journal of Rheumatic Diseases|February 4, 2025
Case Report: Inflammatory Myositis Presenting as Dropped Head Syndrome in a Patient With Rheumatoid AntibodiesEstelle Noonan, Matthew Verheyden, Hwei Choo Soh, et al.
Muscle & Nerve|September 8, 2017
Sarcolemmal excitability in the myotonic dystrophiesRobert Boland-Freitas, James Lee, James Howells, et al.
International Journal of Cardiology|December 26, 2014
Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathyPeter Kabunga, Antony K Lau, Kevin Phan, et al.
Journal of Neurology|July 2, 2013
Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegiaKishore R Kumar, Nicholas F Blair, Himesha Vandebona, et al.
Neuromuscular Disorders : NMD|August 10, 2022
A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centreWui-Kwan Wong, Samantha J Bryen, Adam Bournazos, et al.
HGG Advances|July 18, 2022
Prevalence, parameters, and pathogenic mechanisms for splice-altering acceptor variants that disrupt the AG exclusion zoneSamantha J Bryen, Michaela Yuen, Himanshu Joshi, et al.
The Lancet Regional Health. Western Pacific|November 19, 2024
A contemporary analysis of the Australian clinical and genetic landscape of spinal muscular atrophy: a registry based studyLakshmi Balaji, Robin Forbes, Anita Cairns, et al.
Pageof 4