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Patricia Hafner

Showing results (11-20 of 40) with videos related to

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Trials|March 10, 2017
Treatment with L-citrulline in patients with post-polio syndrome: study protocol for a single-center, randomised, placebo-controlled, double-blind trialSimone Schmidt, Vanya Gocheva, Thomas Zumbrunn, et al.
Muscle & Nerve|March 5, 2015
Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophyUlrike Bonati, Maurice Schmid, Patricia Hafner, et al.
Orphanet Journal of Rare Diseases|March 5, 2021
Standard of care versus new-wave corticosteroids in the treatment of Duchenne muscular dystrophy: Can we do better?Stephanie Kourakis, Cara A Timpani, Dean G Campelj, et al.
Journal of Child Neurology|August 7, 2019
Association Between Health-Related Quality of Life and Motor Function in Ambulant and Nonambulant Duchenne Muscular Dystrophy PatientsVanya Gocheva, Simone Schmidt, Anna-Lena Orsini, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|February 21, 2007
Stimulatory pathways of the Calcium-sensing receptor on acid secretion in freshly isolated human gastric glandsChristine Remy, Philipp Kirchhoff, Patricia Hafner, et al.
Neuromuscular Disorders : NMD|December 19, 2018
Electromyography and muscle biopsy in paediatric neuromuscular disorders - Evaluation of current practice and literature reviewPatricia Hafner, Rahul Phadke, Adnan Manzur, et al.
Plos One|November 14, 2013
Preserved antigen-specific immune response in patients with multiple sclerosis responding to IFNβ-therapyMatthias Mehling, Stefanie Fritz, Patricia Hafner, et al.
Developmental Medicine and Child Neurology|February 7, 2019
Acquired neuromyotonia in children with CASPR2 and LGI1 antibodiesSnehal Surana, Ratna Kumar, Matthew Pitt, et al.
Neuromuscular Disorders : NMD|February 22, 2014
Skeletal muscle MRI of the lower limbs in congenital muscular dystrophy patients with novel POMT1 and POMT2 mutationsPatricia Hafner, Ulrike Bonati, Arne Fischmann, et al.
Journal of Neuromuscular Diseases|March 25, 2025
Automated analysis of quantitative muscle MRI and its reliability in patients with Duchenne muscular dystrophySara Nagy, Olga Kubassova, Patricia Hafner, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Trials|March 10, 2017
Treatment with L-citrulline in patients with post-polio syndrome: study protocol for a single-center, randomised, placebo-controlled, double-blind trialSimone Schmidt, Vanya Gocheva, Thomas Zumbrunn, et al.
Muscle & Nerve|March 5, 2015
Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophyUlrike Bonati, Maurice Schmid, Patricia Hafner, et al.
Orphanet Journal of Rare Diseases|March 5, 2021
Standard of care versus new-wave corticosteroids in the treatment of Duchenne muscular dystrophy: Can we do better?Stephanie Kourakis, Cara A Timpani, Dean G Campelj, et al.
Journal of Child Neurology|August 7, 2019
Association Between Health-Related Quality of Life and Motor Function in Ambulant and Nonambulant Duchenne Muscular Dystrophy PatientsVanya Gocheva, Simone Schmidt, Anna-Lena Orsini, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|February 21, 2007
Stimulatory pathways of the Calcium-sensing receptor on acid secretion in freshly isolated human gastric glandsChristine Remy, Philipp Kirchhoff, Patricia Hafner, et al.
Neuromuscular Disorders : NMD|December 19, 2018
Electromyography and muscle biopsy in paediatric neuromuscular disorders - Evaluation of current practice and literature reviewPatricia Hafner, Rahul Phadke, Adnan Manzur, et al.
Plos One|November 14, 2013
Preserved antigen-specific immune response in patients with multiple sclerosis responding to IFNβ-therapyMatthias Mehling, Stefanie Fritz, Patricia Hafner, et al.
Developmental Medicine and Child Neurology|February 7, 2019
Acquired neuromyotonia in children with CASPR2 and LGI1 antibodiesSnehal Surana, Ratna Kumar, Matthew Pitt, et al.
Neuromuscular Disorders : NMD|February 22, 2014
Skeletal muscle MRI of the lower limbs in congenital muscular dystrophy patients with novel POMT1 and POMT2 mutationsPatricia Hafner, Ulrike Bonati, Arne Fischmann, et al.
Journal of Neuromuscular Diseases|March 25, 2025
Automated analysis of quantitative muscle MRI and its reliability in patients with Duchenne muscular dystrophySara Nagy, Olga Kubassova, Patricia Hafner, et al.
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