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B Waddell

Showing results (21-30 of 65) with videos related to

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Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Journal of Clinical Microbiology|December 15, 2015
Development and Validation of a PCR Assay To Detect the Prairie Epidemic Strain of Pseudomonas aeruginosa from Patients with Cystic FibrosisM Workentine, A Poonja, B Waddell, et al.
Open Forum Infectious Diseases|January 25, 2020
Clinical Outcomes Associated With <i>Escherichia coli</i> Infections in Adults With Cystic Fibrosis: A Cohort StudyB D Edwards, R Somayaji, J Greysson-Wong, et al.
Journal of Clinical Microbiology|April 28, 2017
Prevalence and Outcomes of Achromobacter Species Infections in Adults with Cystic Fibrosis: a North American Cohort StudyB D Edwards, J Greysson-Wong, R Somayaji, et al.
Frontiers in Neurology|February 13, 2023
Case report: Adult-onset limb girdle muscular dystrophy in sibling pair due to novel homozygous <i>LAMA2</i> missense variantMatthew Katz, Leigh B Waddell, Michaela Yuen, et al.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
Neurology|March 10, 2012
Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5S Penttilä, J Palmio, T Suominen, et al.
Muscle & Nerve|June 16, 2011
Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiencyEppie M Yiu, Alfred Klausegger, Leigh B Waddell, 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.
Neuromuscular Disorders : NMD|June 21, 2011
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patientsLeigh B Waddell, Jenny Tran, Xi F Zheng, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Journal of Clinical Microbiology|December 15, 2015
Development and Validation of a PCR Assay To Detect the Prairie Epidemic Strain of Pseudomonas aeruginosa from Patients with Cystic FibrosisM Workentine, A Poonja, B Waddell, et al.
Open Forum Infectious Diseases|January 25, 2020
Clinical Outcomes Associated With <i>Escherichia coli</i> Infections in Adults With Cystic Fibrosis: A Cohort StudyB D Edwards, R Somayaji, J Greysson-Wong, et al.
Journal of Clinical Microbiology|April 28, 2017
Prevalence and Outcomes of Achromobacter Species Infections in Adults with Cystic Fibrosis: a North American Cohort StudyB D Edwards, J Greysson-Wong, R Somayaji, et al.
Frontiers in Neurology|February 13, 2023
Case report: Adult-onset limb girdle muscular dystrophy in sibling pair due to novel homozygous <i>LAMA2</i> missense variantMatthew Katz, Leigh B Waddell, Michaela Yuen, et al.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
Neurology|March 10, 2012
Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5S Penttilä, J Palmio, T Suominen, et al.
Muscle & Nerve|June 16, 2011
Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiencyEppie M Yiu, Alfred Klausegger, Leigh B Waddell, 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.
Neuromuscular Disorders : NMD|June 21, 2011
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patientsLeigh B Waddell, Jenny Tran, Xi F Zheng, et al.
Pageof 7