Search Results - "Thiele, Simone"

Successful pregnancy of an SMA type 3 sitter on Nusinersen therapy - a case report.

Authors: Hiebeler, Miriam Thiele, Simone Walter, Maggie C.

Source: BMC Neurology. 1/4/2025, Vol. 25 Issue 1, p1-7. 7p.

Health-related quality of life of adults with spinal muscular atrophy: insights from a nationwide patient registry in Germany.

Authors: Landfeldt, Erik Leibrock, Berenike Hussong, Justine et al.

Source: Quality of Life Research. Jul2024, Vol. 33 Issue 7, p1949-1959. 11p.

Subjects: Spinal muscular atrophy, Quality of life, Adults, Medical registries, Neuromuscular diseases, Life expectancy, Trauma registries, Neuromuscular transmission

Geographic Terms: Germany

Disease spectrum and long-term prognosis of patients with BAG3-associated neuromuscular diseases in Europe.

Authors: Fernández-Eulate, Gorka Gitiaux, Cyril Thiele, Simone et al.

Source: Brain: A Journal of Neurology; Dec2025, Vol. 148 Issue 12, p4435-4447, 13p

Cost of illness in inclusion body myositis: results from a cross-sectional study in Germany.

Authors: Senn, Katja C. Thiele, Simone Kummer, Karsten et al.

Source: Orphanet Journal of Rare Diseases. 10/11/2023, Vol. 18 Issue 1, p1-15. 15p.

Inclusion body myositis—health-related quality of life and care situation during phases of the "patience journey" in Germany: results from a qualitative study.

Authors: Senn, Katja C. Thiele, Simone Gumbert, Laura et al.

Source: Health & Quality of Life Outcomes. 10/10/2023, Vol. 21 Issue 1, p1-11. 11p.

Patient-Reported Health-Related Quality of Life, Anxiety and Depression in Patients with Inclusion Body Myositis: A Register-Based Cross-Sectional Study in Germany.

Authors: Senn, Katja C. Thiele, Simone Kummer, Karsten et al.

Source: Journal of Clinical Medicine. Aug2023, Vol. 12 Issue 15, p5051. 18p.

Time to diagnosis of Duchenne muscular dystrophy in Austria and Germany.

Authors: Hiebeler, Miriam Thiele, Simone Reilich, Peter et al.

Source: Scientific Reports. 1/5/2023, Vol. 13 Issue 1, p1-8. 8p.

Long-term whole-body vibration training in two late-onset Pompe disease patients.

Authors: Montagnese, Federica Thiele, Simone Wenninger, Stephan et al.

Source: Neurological Sciences. Aug2016, Vol. 37 Issue 8, p1357-1360. 4p.

Subjects: Whole-body vibration, Vibration (Mechanics), Glycogen storage disease type II, Applied kinesiology, Pulmonary function tests, Patients

The health-related quality of life, mental health and mental illnesses of patients with inclusion body myositis (IBM): results of a mixed methods systematic review.

Authors: Senn, Katja C. Gumbert, Laura Thiele, Simone et al.

Source: Orphanet Journal of Rare Diseases. 6/16/2022, Vol. 17 Issue 1, p1-15. 15p.

Influence of macular oedema on the measurement of macular pigment optical density.

Authors: Thiele, Simone Rauscher, Franziska Wiedemann, Peter et al.

Source: Graefe's Archive of Clinical & Experimental Ophthalmology. Mar2016, Vol. 254 Issue 3, p455-465. 11p.

De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in Germany.

Authors: König, Kirsten Pechmann, Astrid Thiele, Simone et al.

Source: Orphanet Journal of Rare Diseases. 6/24/2019, Vol. 14 Issue 1, p1-7. 7p.

Disease burden of spinal muscular atrophy in Germany.

Authors: Klug, Constanze Schreiber-Katz, Olivia Thiele, Simone et al.

Source: Orphanet Journal of Rare Diseases. 5/4/2016, Vol. 11, p1-9. 9p.

Comparative cost of illness analysis and assessment of health care burden of Duchenne and Becker muscular dystrophies in Germany.

Authors: Schreiber-Katz, Olivia Klug, Constanze Thiele, Simone et al.

Source: Orphanet Journal of Rare Diseases. 2014, Vol. 9 Issue 1, p441-464. 24p.

Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.

Authors: Walter, Maggie C. Reilich, Peter Thiele, Simone et al.

Source: Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, Special section p1-15. 15p. 1 Color Photograph, 1 Diagram, 5 Charts, 1 Graph.

Areas of improvement in the medical care of SMA: evidence from a nationwide patient registry in Germany.

Authors: Leibrock, Berenike Landfeldt, Erik Hussong, Justine et al.

Source: Orphanet Journal of Rare Diseases. 2/21/2023, Vol. 18 Issue 1, p1-10. 10p.

Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy – A patients' perspective.

Authors: Janisch, Maria Boehme, Kristin Thiele, Simone et al.

Source: Neuromuscular Disorders. Dec2020, Vol. 30 Issue 12, p975-985. 11p.

De-duplicating Patient Records from Three Independent Data Sources Reveals the Incidence of Rare Neuromuscular Disorders in Germany.

Authors: Pechmann, Astrid König, Kirsten Thiele, Simone et al.

Source: Neuropediatrics. 2019 Supplement2, Vol. 50, pS1-S55. 55p.

Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy.

Authors: Borland, Holly Moore, Ursula Dressman, Heather Gordish et al.

Source: Neuromuscular Disorders. Oct2024, Vol. 43, p20-28. 9p.

Global FKRP Registry: observations in more than 300 patients with Limb Girdle Muscular Dystrophy R9.

Authors: Murphy, Lindsay B. Schreiber‐Katz, Olivia Rafferty, Karen et al.

Source: Annals of Clinical & Translational Neurology. May2020, Vol. 7 Issue 5, p757-766. 10p.

Measuring health-related quality of life in spinal muscular atrophy – Lessons learned from a Nationwide registry study in Germany.

Authors: Landfeldt, Erik Leibrock, Berenike Hussong, Justine et al.

Source: Journal of the Neurological Sciences. Nov2025, Vol. 478, pN.PAG-N.PAG. 1p.