Canlyniadau Chwilio - Thomas Voit

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  1. 1
    Non‐invasive ventilation reduces respiratory tract infections in children with neuromuscular disorders

    Non‐invasive ventilation reduces respiratory tract infections in children with neuromuscular disorders gan C. Dohna‐Schwake, P. Podlewski, Thomas Voït, Uwe Mellies

    Cyhoeddwyd 2007
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  2. 2
    Direct visualization of the dystrophin network on skeletal muscle fiber membrane.

    Direct visualization of the dystrophin network on skeletal muscle fiber membrane. gan Volker Straub, Reginald E. Bittner, J. Léger, Thomas Voit

    Cyhoeddwyd 1992
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  3. 3
    Long­term noninvasive ventilation in children and adolescents with neuromuscular disorders

    Long­term noninvasive ventilation in children and adolescents with neuromuscular disorders gan Uwe Mellies, R. Ragette, C. Schwake, Holger Boehm, Thomas Voit, Helmut Teschler

    Cyhoeddwyd 2003
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  4. 4
    Antisense targeting of 3′ end elements involved in<i>DUX4</i>mRNA processing is an efficient therapeutic strategy for facioscapulohumeral dystrophy: a new gene-silencing approach

    Antisense targeting of 3′ end elements involved in<i>DUX4</i>mRNA processing is an efficient therapeutic strategy for facioscapulohumeral dystrophy: a new gene-silencing approach gan Anne-Charlotte Marsollier, Lukasz Ciszewski, Virginie Mariot, Linda Popplewell, Thomas Voit, George Dickson, Julie Dumonceaux

    Cyhoeddwyd 2016
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  5. 5
    Defective protein glycosylation in patients with cutis laxa syndrome

    Defective protein glycosylation in patients with cutis laxa syndrome gan Éva Morava, Suzan Wopereis, Paul Coucke, Gabrielle Gillessen-Kaesbach, Thomas Voit, Jan Smeitink, Ron A. Wevers, Stephanie Grünewald

    Cyhoeddwyd 2005
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  6. 6
    AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy

    AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy gan Maëva Le Hir, Aurélie Goyenvalle, Cécile Peccate, Guillaume Précigout, Kay E. Davies, Thomas Voït, Luis Garcı́a, Stéphanie Lorain

    Cyhoeddwyd 2013
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  7. 7
    Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy

    Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy gan Ralf Herrmann, Volker Straub, Martina Blank, C. Kutzick, N. Franke, Ebor Jacob, H. G. Lenard, Stephan Kröger, Thomas Voit

    Cyhoeddwyd 2000
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  8. 8
    Repair of Rhodopsin mRNA by Spliceosome-Mediated RNA Trans -Splicing: A New Approach for Autosomal Dominant Retinitis Pigmentosa

    Repair of Rhodopsin mRNA by Spliceosome-Mediated RNA Trans -Splicing: A New Approach for Autosomal Dominant Retinitis Pigmentosa gan Adeline Berger, Stéphanie Lorain, Charlène Joséphine, Mélissa Desrosiers, Cécile Peccate, Thomas Voit, Luis Garcı́a, José‐Alain Sahel, Alexis‐Pierre Bemelmans

    Cyhoeddwyd 2015
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  9. 9
    Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; Report of three expert workshops: TREAT-NMD/ENMC Workshop on outcome measures, 12th–13th May 2007, Naarden, The Netherlands; TREAT-NMD Workshop on outcome measures in experimental trials for DMD, 30th June–1st July 2007, Naarden, The Netherlands; Conjoint Institute of Myology TREAT-NMD Meeting on physical activity monitoring in neuromuscular disorders, 11th July 2007, Paris, France

    Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; Report of three expert workshops: TREAT-NMD/ENMC Workshop on outcome measures, 12th–13th May 2007, Naard... gan Eugenio Mercuri, Anna Mayhew, Francesco Muntoni, Sonia Messina, Volker Straub, G J van Ommen, Thomas Voit, Enrico Bertini, Kate Bushby

    Cyhoeddwyd 2008
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  10. 10
    Acute Fluid Intake Impacts Assessment of Body Composition via Bioelectrical Impedance Analysis. A Randomized, Controlled Crossover Pilot Trial

    Acute Fluid Intake Impacts Assessment of Body Composition via Bioelectrical Impedance Analysis. A Randomized, Controlled Crossover Pilot Trial gan Janis Schierbauer, Svenja Günther, Sandra Haupt, Rebecca T. Zimmer, Daniel Herz, Thomas Voït, Paul Zimmermann, Nadine Wachsmuth, Felix Aberer, Othmar Moser

    Cyhoeddwyd 2023
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  11. 11
    Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis

    Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis gan Uwe Kornak, Ansgar Schulz, W Friedrich, Siegfried Uhlhaas, B Kremens, Thomas Voït, Carola Hasan, U. Bode, Thomas J. Jentsch, Christian Kubisch

    Cyhoeddwyd 2000
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  12. 12
    Cholesterol metabolism is a potential therapeutic target in Duchenne muscular dystrophy

    Cholesterol metabolism is a potential therapeutic target in Duchenne muscular dystrophy gan Fatima Amor, Ai Vu Hong, Guillaume Corre, Mathilde Sanson, Laurence Suel, Stéphanie Blaie, Laurent Servais, Thomas Voit, Isabelle Richard, David Israeli

    Cyhoeddwyd 2021
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  13. 13
    Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines

    Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines gan Matthew Thorley, Stéphanie Duguez, Emilia Maria Cristina Mazza, Sara Valsoni, Anne Bigot, Kamel Mamchaoui, Brennan Harmon, Thomas Voït, Vincent Mouly, William Duddy

    Cyhoeddwyd 2016
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  14. 14
    Efficacy of Fasting in Type 1 and Type 2 Diabetes Mellitus: A Narrative Review

    Efficacy of Fasting in Type 1 and Type 2 Diabetes Mellitus: A Narrative Review gan Daniel Herz, Sandra Haupt, Rebecca T. Zimmer, Nadine Wachsmuth, Janis Schierbauer, Paul Zimmermann, Thomas Voït, Ulrike Thurm, Kayvan Khoramipour, Siân Rilstone, Othmar Moser

    Cyhoeddwyd 2023
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  15. 15
    A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and <i>mdx</i> mice Immunological evidence

    A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and <i>mdx</i> mice Immunological evidence gan F. Pons, N Augier, Jocelyne Léger, Aude Robert, F.M.S. Tomé, Michel Fardeau, Thomas Voit, L. V. B. Nicholson, Dominique Mornet, J. Léger

    Cyhoeddwyd 1991
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  16. 16
    A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment

    A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment gan Anne‐Gaëlle Le Moing, A. Seferian, A. Moraux, M. Annoussamy, Éric Dorveaux, E. Gasnier, Jean‐Yves Hogrel, Thomas Voit, David Vissière, Laurent Servais

    Cyhoeddwyd 2016
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  17. 17
    Manual segmentation of individual muscles of the quadriceps femoris using MRI: A reappraisal

    Manual segmentation of individual muscles of the quadriceps femoris using MRI: A reappraisal gan Yoann Barnouin, Gillian Butler‐Browne, Thomas Voit, David Reversat, Noura Azzabou, Gaëlle Leroux, Anthony Béhin, Jamie S. McPhee, Pierre G. Carlier, Jean‐Yves Hogrel

    Cyhoeddwyd 2013
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  18. 18
    Serum Profiling Identifies Novel Muscle miRNA and Cardiomyopathy-Related miRNA Biomarkers in Golden Retriever Muscular Dystrophy Dogs and Duchenne Muscular Dystrophy Patients

    Serum Profiling Identifies Novel Muscle miRNA and Cardiomyopathy-Related miRNA Biomarkers in Golden Retriever Muscular Dystrophy Dogs and Duchenne Muscular Dystrophy Patients gan Laurence Jeanson-Leh, Julie Lameth, Soraya Krimi, Julien Buisset, Fatima Amor, Caroline Le Guiner, Inès Barthélémy, Laurent Servais, Stéphane Blot, Thomas Voit, David Israeli

    Cyhoeddwyd 2014
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  19. 19
    Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy

    Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy gan Phillipa J. Lamont, B. Udd, Francis Mastaglia, Marjolein Visser, Peter Hedera, Thomas Voït, Leslie Bridges, V. Fabian, Annemieke J.M. Rozemüller, Nigel G. Laing

    Cyhoeddwyd 2005
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  20. 20
    A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model

    A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model gan Maria Grazia Biferi, Mathilde Cohen-Tannoudji, Ambra Cappelletto, Benoit Giroux, Marianne Roda, Stéphanie Astord, Thibaut Marais, Corinne Bos, Thomas Voit, Arnaud Ferry, Martine Barkats

    Cyhoeddwyd 2017
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