Результати пошуку - Janbernd Kirschner
- Показ 1 - 20 результатів із 68
- На наступну сторінку
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Duchenne muscular dystrophy and caregiver burden: a systematic review за авторством Erik Landfeldt, Josefin Edström, Filippo Buccella, Janbernd Kirschner, Hanns Lochmüller
Опубліковано 2018Revisão -
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Mitochondrial Tubulopathy in Tenofovir Disoproxil Fumarate-Treated Rats за авторством Dirk Lebrecht, Ana C Venhoff, Janbernd Kirschner, Thorsten Wiech, Nils Venhoff, Ulrich A. Walker
Опубліковано 2009Artigo -
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Safety Monitoring of Gene Therapy for Spinal Muscular Atrophy with Onasemnogene Abeparvovec –A Single Centre Experience за авторством Johannes Friese, Stephanie Geitmann, Dorothea Holzwarth, Nicole Müller, Robert Sassen, Ute Baur, Kristin Adler, Janbernd Kirschner
Опубліковано 2021Artigo -
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Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis за авторством Erik Landfeldt, Alicia Alemán, Sophia Abner, Rongrong Zhang, Christian Werner, Ioannis Tomazos, Nermina Ferizović, Hanns Lochmüller, Janbernd Kirschner
Опубліковано 2024Revisão -
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Adult care for Duchenne muscular dystrophy in the UK за авторством Sunil Rodger, Katherine L. Woods, Catherine L. Bladen, Angela Stringer, Julia Vry, K. Gramsch, Janbernd Kirschner, Rachel Thompson, K. Bushby, Hanns Lochmüller
Опубліковано 2014Artigo -
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A multi-source approach to determine SMA incidence and research ready population за авторством Ingrid E.C. Verhaart, Agata Robertson, Rebecca Leary, Grace McMacken, Kirsten König, Janbernd Kirschner, Cynthia C. Jones, Suzanne F. Cook, Hanns Lochmüller
Опубліковано 2017Artigo -
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Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 – A Prospective Observational Study за авторством Maggie C. Walter, Stephan Wenninger, Simone Thiele, Julia M. Stauber, Miriam Hiebeler, Eva Greckl, Kristina Ståhl, Astrid Pechmann, Hanns Lochmüller, Janbernd Kirschner, Benedikt Schoser
Опубліковано 2019Artigo -
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SMArtCARE - A platform to collect real-life outcome data of patients with spinal muscular atrophy за авторством Astrid Pechmann, Kirsten König, G. Bernert, Kristina Schachtrup, Ulrike Schara, David Schorling, Inge Schwersenz, Sabine Stein, Adrian Tassoni, Sibylle Emilie Vogt, Maggie C. Walter, Hanns Lochmüller, Janbernd Kirschner
Опубліковано 2019Artigo -
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Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany за авторством Astrid Pechmann, Thorsten Langer, David Schorling, Sabine Stein, Sibylle Emilie Vogt, Ulrike Schara, Heike Kölbel, Oliver Schwartz, Andreas Hahn, Kerstin Giese, Jessika Johannsen, Jonas Denecke, Claudia Weiß, Manuela Theophil, Janbernd Kirschner
Опубліковано 2018Artigo -
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European ad-hoc consensus statement on gene replacement therapy for spinal muscular atrophy за авторством Janbernd Kirschner, Nina Butoianu, Nathalie Goemans, Jana Haberlová, Anna Kostera‐Pruszczyk, Eugenio Mercuri, W. Ludo van der Pol, Susana Quijano‐Roy, Thomas Sejersen, Eduardo F. Tizzano, Andreas Ziegler, Laurent Servais, Francesco Muntoni
Опубліковано 2020Artigo -
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JEWELFISH: 24-month results from an open-label study in non-treatment-naïve patients with SMA receiving treatment with risdiplam за авторством Claudia A. Chiriboga, Claudio Bruno, Tina Duong, Dirk Fischer, Eugenio Mercuri, Janbernd Kirschner, Anna Kostera‐Pruszczyk, Birgit Jaber, Ksenija Gorni, Heidemarie Kletzl, Imogen Carruthers, Carmen Martín, R. Scalco, Paulo Fontoura, Francesco Muntoni
Опубліковано 2024Artigo -
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Combination disease‐modifying treatment in spinal muscular atrophy: A proposed classification за авторством Crystal M. Proud, Eugenio Mercuri, Richard S. Finkel, Janbernd Kirschner, Darryl C. De Vivo, Francesco Muntoni, Kayoko Saito, Eduardo F. Tizzano, Isabelle Desguerre, Susana Quijano‐Roy, Kamal Benguerba, Dheeraj Raju, Eric Faulkner, Laurent Servais
Опубліковано 2023Artigo -
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Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies за авторством Magdolna Nagy, Tom G. Mastenbroek, Nadine J.A. Mattheij, Susanne Witt, Kenneth J. Clemetson, Janbernd Kirschner, Ansgar Schulz, Thomas Vraetz, Carsten Speckmann, Attila Braun, Judith M.E.M. Cosemans, Barbara Zieger, Johan W. M. Heemskerk
Опубліковано 2017Artigo -
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A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies за авторством Marina Bartsakoulia, Angela Pyle, Diego Troncoso-Chandía, Josefa Vial-Brizzi, Marysol V. Paz-Fiblas, Jennifer Duff, Helen Griffin, Veronika Boczonadi, Hanns Lochmüller, Stephanie Kleinle, Patrick F. Chinnery, Sarah C. Grünert, Janbernd Kirschner, Verónica Eisner, Rita Horváth
Опубліковано 2018Artigo -
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ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia за авторством Christie‐Ann McCarl, Capucine Pïcard, Sara Khalil, Takumi Kawasaki, Jens Röther, Alexander Papolos, Jeffery L. Kutok, Claire Hivroz, F Ledeist, Katrin Plogmann, Stephan Ehl, Gundula Notheis, Michael H. Albert, Bernd H. Belohradsky, Janbernd Kirschner, Anjana Rao, Alain Fischer, Stefan Feske
Опубліковано 2009Artigo -
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Safety and effectiveness of ataluren in patients with nonsense mutation DMD in the STRIDE Registry compared with the CINRG Duchenne Natural History Study (2015–2022): 2022 interim... за авторством Eugenio Mercuri, A. Nascimento Osorio, Francesco Muntoni, Filippo Buccella, Isabelle Desguerre, Janbernd Kirschner, M. Tulinius, Maria Bernadete Dutra de Resende, Lauren P. Morgenroth, Heather Gordish‐Dressman, Shelley Johnson, Allan Kristensen, Christian Werner, Panayiota Trifillis, Erik Henricson, Craig M. McDonald
Опубліковано 2023Artigo -
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Correction to: Safety and effectiveness of ataluren in patients with nonsense mutation DMD in the STRIDE Registry compared with the CINRG Duchenne Natural History Study (2015–2022)... за авторством Eugenio Mercuri, A. Nascimento Osorio, Francesco Muntoni, Filippo Buccella, Isabelle Desguerre, Janbernd Kirschner, M. Tulinius, Maria Bernadete Dutra de Resende, Lauren P. Morgenroth, Heather Gordish‐Dressman, Shelley Johnson, Allan Kristensen, Christian Werner, Panayiota Trifillis, Erik Henricson, Craig M. McDonald
Опубліковано 2023Errata/Corrigenda -
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A Combined Laser Microdissection and Mass Spectrometry Approach Reveals New Disease Relevant Proteins Accumulating in Aggregates of Filaminopathy Patients за авторством Rudolf A. Kley, A. Maerkens, Yvonne Leber, Verena Theis, Anja Schreiner, Peter F. M. van der Ven, Julian Uszkoreit, Christoph Stephan, Stefan Eulitz, Nicole Euler, Janbernd Kirschner, Klaus Müller, Helmut E. Meyer, Martin Tegenthoff, Dieter O. Fürst, Matthias Vorgerd, Thorsten Müller, Katrin Marcus
Опубліковано 2012Artigo
Інструменти для пошуку:
Пов'язані теми
Medicine
Internal medicine
Biology
Disease
Spinal muscular atrophy
Physical therapy
Gene
Genetics
Pathology
Pediatrics
SMA*
Duchenne muscular dystrophy
Physical medicine and rehabilitation
Combinatorics
Mathematics
Clinical trial
Mutation
Environmental health
Population
Cell biology
Alternative medicine
Adverse effect
Computer science
Endocrinology
Muscular dystrophy
Placebo
Surgery
Archaeology
Neuromuscular disease
SMN1