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Trials
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March 10, 2017
Treatment with L-citrulline in patients with post-polio syndrome: study protocol for a single-center, randomised, placebo-controlled, double-blind trial
Simone Schmidt, Vanya Gocheva, Thomas Zumbrunn, et al.
Muscle & Nerve
|
March 5, 2015
Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophy
Ulrike 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 Patients
Vanya 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 glands
Christine 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 review
Patricia 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-therapy
Matthias Mehling, Stefanie Fritz, Patricia Hafner, et al.
Developmental Medicine and Child Neurology
|
February 7, 2019
Acquired neuromyotonia in children with CASPR2 and LGI1 antibodies
Snehal 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 mutations
Patricia 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 dystrophy
Sara Nagy, Olga Kubassova, Patricia Hafner, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 40) with videos related to
Sort By:
Page
of 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 trial
Simone Schmidt, Vanya Gocheva, Thomas Zumbrunn, et al.
Muscle & Nerve
|
March 5, 2015
Longitudinal 2-point dixon muscle magnetic resonance imaging in becker muscular dystrophy
Ulrike 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 Patients
Vanya 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 glands
Christine 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 review
Patricia 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-therapy
Matthias Mehling, Stefanie Fritz, Patricia Hafner, et al.
Developmental Medicine and Child Neurology
|
February 7, 2019
Acquired neuromyotonia in children with CASPR2 and LGI1 antibodies
Snehal 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 mutations
Patricia 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 dystrophy
Sara Nagy, Olga Kubassova, Patricia Hafner, et al.
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