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Thomas Krag

Showing results (11-20 of 43) with videos related to

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Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
Physiological Reports|January 7, 2026
Lactate increases oxygen unloading of preconditioned blood from male elite breath-hold diversThomas Kjeld, Egon Godthaab Hansen, Henrik Christian Arendrup, et al.
Neuromuscular Disorders : NMD|August 1, 2018
BAG3 myopathy is not always associated with cardiomyopathyAnnarita Ghosh Andersen, Freja Fornander, Henrik Daa Schrøder, et al.
Muscle & Nerve|January 18, 2018
Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblastsNanna Witting, Thomas Krag, Ulla Werlauff, et al.
Muscle & Nerve|September 22, 2021
Muscle biopsy and MRI findings in ANO5-related myopathySonja Holm-Yildiz, Nanna Witting, Josefine de Stricker Borch, et al.
Brain : a Journal of Neurology|July 4, 2006
Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathyTina D Jeppesen, Marianne Schwartz, David B Olsen, et al.
Human Mutation|April 14, 2025
Variants in CAPN3 Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy Combined With Calpain-3 DeficiencyThomas Krag, Emily Nasho, Lauren Brady, et al.
Neuromuscular Disorders : NMD|October 29, 2013
A novel de novo mutation of the mitochondrial tRNAlys gene mt.8340G>a associated with pure myopathyTina Dysgaard Jeppesen, Morten Duno, Lotte Risom, et al.
Neuromuscular Disorders : NMD|June 14, 2023
Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophyMaria Barington, Morten Dunø, Ulf Birkedal, et al.
Journal of Clinical Medicine|July 16, 2020
Preserved Capacity for Adaptations in Strength and Muscle Regulatory Factors in Elderly in Response to Resistance Exercise Training and DeconditioningAndreas Mæchel Fritzen, Frank D Thøgersen, Khaled Abdul Nasser Qadri, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
Physiological Reports|January 7, 2026
Lactate increases oxygen unloading of preconditioned blood from male elite breath-hold diversThomas Kjeld, Egon Godthaab Hansen, Henrik Christian Arendrup, et al.
Neuromuscular Disorders : NMD|August 1, 2018
BAG3 myopathy is not always associated with cardiomyopathyAnnarita Ghosh Andersen, Freja Fornander, Henrik Daa Schrøder, et al.
Muscle & Nerve|January 18, 2018
Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblastsNanna Witting, Thomas Krag, Ulla Werlauff, et al.
Muscle & Nerve|September 22, 2021
Muscle biopsy and MRI findings in ANO5-related myopathySonja Holm-Yildiz, Nanna Witting, Josefine de Stricker Borch, et al.
Brain : a Journal of Neurology|July 4, 2006
Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathyTina D Jeppesen, Marianne Schwartz, David B Olsen, et al.
Human Mutation|April 14, 2025
Variants in CAPN3 Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy Combined With Calpain-3 DeficiencyThomas Krag, Emily Nasho, Lauren Brady, et al.
Neuromuscular Disorders : NMD|October 29, 2013
A novel de novo mutation of the mitochondrial tRNAlys gene mt.8340G>a associated with pure myopathyTina Dysgaard Jeppesen, Morten Duno, Lotte Risom, et al.
Neuromuscular Disorders : NMD|June 14, 2023
Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophyMaria Barington, Morten Dunø, Ulf Birkedal, et al.
Journal of Clinical Medicine|July 16, 2020
Preserved Capacity for Adaptations in Strength and Muscle Regulatory Factors in Elderly in Response to Resistance Exercise Training and DeconditioningAndreas Mæchel Fritzen, Frank D Thøgersen, Khaled Abdul Nasser Qadri, et al.
Pageof 5