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Orphanet Journal of Rare Diseases
|
June 26, 2019
De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in Germany
Kirsten König, Astrid Pechmann, Simone Thiele, et al.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen
|
August 29, 2022
Thorsten Langer, Nicole Gusset, Astrid Pechmann, et al.
Brain Stimulation
|
November 1, 2011
The number of full-sine cycles per pulse influences the efficacy of multicycle transcranial magnetic stimulation
Astrid Pechmann, Igor Delvendahl, Til O Bergmann, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 2, 2020
Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey
David C Schorling, Cornelia K Müller, Astrid Pechmann, et al.
Orphanet Journal of Rare Diseases
|
September 26, 2024
Postnatal management of preterm infants with spinal muscular atrophy: experience from German newborn screening
Regina Trollmann, Jessika Johannsen, Katharina Vill, et al.
Orphanet Journal of Rare Diseases
|
August 13, 2025
Epidemiology, disease burden and costs of Duchenne muscular dystrophy in Germany: an observational, retrospective health claims data analysis
Joanna Diesing, Janbernd Kirschner, Astrid Pechmann, et al.
International Journal of Molecular Sciences
|
September 9, 2023
Whole-Genome Sequencing Identified New Structural Variations in the <i>DMD</i> Gene That Cause Duchenne Muscular Dystrophy in Two Girls
Natalie Pluta, Arpad von Moers, Astrid Pechmann, et al.
Frontiers in Pediatrics
|
October 9, 2023
Evaluating case management for caregivers of children with spinal muscular atrophy type I and II-an exploratory, controlled, mixed-methods trial
Jana Willems, Astrid Pechmann, Sabine Wider, et al.
Journal of Neuromuscular Diseases
|
October 10, 2019
Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 - A Prospective Observational Study
Maggie C Walter, Stephan Wenninger, Simone Thiele, et al.
Journal of Neuromuscular Diseases
|
August 20, 2025
Physiotherapeutic management of patients with SMA: A questionnaire-based online survey among physiotherapists within the SMArtCARE network
Sibylle Vogt, Cornelia Voigt-Müller, Heidi Rochau-Trumpp, et al.
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of 6
Search research articles
Search
Showing results (21-30 of 55) with videos related to
Sort By:
Page
of 6
Orphanet Journal of Rare Diseases
|
June 26, 2019
De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in Germany
Kirsten König, Astrid Pechmann, Simone Thiele, et al.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen
|
August 29, 2022
Thorsten Langer, Nicole Gusset, Astrid Pechmann, et al.
Brain Stimulation
|
November 1, 2011
The number of full-sine cycles per pulse influences the efficacy of multicycle transcranial magnetic stimulation
Astrid Pechmann, Igor Delvendahl, Til O Bergmann, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
July 2, 2020
Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey
David C Schorling, Cornelia K Müller, Astrid Pechmann, et al.
Orphanet Journal of Rare Diseases
|
September 26, 2024
Postnatal management of preterm infants with spinal muscular atrophy: experience from German newborn screening
Regina Trollmann, Jessika Johannsen, Katharina Vill, et al.
Orphanet Journal of Rare Diseases
|
August 13, 2025
Epidemiology, disease burden and costs of Duchenne muscular dystrophy in Germany: an observational, retrospective health claims data analysis
Joanna Diesing, Janbernd Kirschner, Astrid Pechmann, et al.
International Journal of Molecular Sciences
|
September 9, 2023
Whole-Genome Sequencing Identified New Structural Variations in the <i>DMD</i> Gene That Cause Duchenne Muscular Dystrophy in Two Girls
Natalie Pluta, Arpad von Moers, Astrid Pechmann, et al.
Frontiers in Pediatrics
|
October 9, 2023
Evaluating case management for caregivers of children with spinal muscular atrophy type I and II-an exploratory, controlled, mixed-methods trial
Jana Willems, Astrid Pechmann, Sabine Wider, et al.
Journal of Neuromuscular Diseases
|
October 10, 2019
Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 - A Prospective Observational Study
Maggie C Walter, Stephan Wenninger, Simone Thiele, et al.
Journal of Neuromuscular Diseases
|
August 20, 2025
Physiotherapeutic management of patients with SMA: A questionnaire-based online survey among physiotherapists within the SMArtCARE network
Sibylle Vogt, Cornelia Voigt-Müller, Heidi Rochau-Trumpp, et al.
Page
of 6