Torthaí cuardaigh - Thomas Voit
- 1 - 20 toradh as 81 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Non‐invasive ventilation reduces respiratory tract infections in children with neuromuscular disorders de réir C. Dohna‐Schwake, P. Podlewski, Thomas Voït, Uwe Mellies
Foilsithe / Cruthaithe 2007Artigo -
2
Direct visualization of the dystrophin network on skeletal muscle fiber membrane. de réir Volker Straub, Reginald E. Bittner, J. Léger, Thomas Voit
Foilsithe / Cruthaithe 1992Artigo -
3
Longterm noninvasive ventilation in children and adolescents with neuromuscular disorders de réir Uwe Mellies, R. Ragette, C. Schwake, Holger Boehm, Thomas Voit, Helmut Teschler
Foilsithe / Cruthaithe 2003Artigo -
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 de réir Anne-Charlotte Marsollier, Lukasz Ciszewski, Virginie Mariot, Linda Popplewell, Thomas Voit, George Dickson, Julie Dumonceaux
Foilsithe / Cruthaithe 2016Artigo -
5
Defective protein glycosylation in patients with cutis laxa syndrome de réir Éva Morava, Suzan Wopereis, Paul Coucke, Gabrielle Gillessen-Kaesbach, Thomas Voit, Jan Smeitink, Ron A. Wevers, Stephanie Grünewald
Foilsithe / Cruthaithe 2005Artigo -
6
AAV Genome Loss From Dystrophic Mouse Muscles During AAV-U7 snRNA-mediated Exon-skipping Therapy de réir Maëva Le Hir, Aurélie Goyenvalle, Cécile Peccate, Guillaume Précigout, Kay E. Davies, Thomas Voït, Luis Garcı́a, Stéphanie Lorain
Foilsithe / Cruthaithe 2013Artigo -
7
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy de réir Ralf Herrmann, Volker Straub, Martina Blank, C. Kutzick, N. Franke, Ebor Jacob, H. G. Lenard, Stephan Kröger, Thomas Voit
Foilsithe / Cruthaithe 2000Artigo -
8
Repair of Rhodopsin mRNA by Spliceosome-Mediated RNA Trans -Splicing: A New Approach for Autosomal Dominant Retinitis Pigmentosa de réir Adeline Berger, Stéphanie Lorain, Charlène Joséphine, Mélissa Desrosiers, Cécile Peccate, Thomas Voit, Luis Garcı́a, José‐Alain Sahel, Alexis‐Pierre Bemelmans
Foilsithe / Cruthaithe 2015Artigo -
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, Naard... de réir Eugenio Mercuri, Anna Mayhew, Francesco Muntoni, Sonia Messina, Volker Straub, G J van Ommen, Thomas Voit, Enrico Bertini, Kate Bushby
Foilsithe / Cruthaithe 2008Artigo -
10
Acute Fluid Intake Impacts Assessment of Body Composition via Bioelectrical Impedance Analysis. A Randomized, Controlled Crossover Pilot Trial de réir Janis Schierbauer, Svenja Günther, Sandra Haupt, Rebecca T. Zimmer, Daniel Herz, Thomas Voït, Paul Zimmermann, Nadine Wachsmuth, Felix Aberer, Othmar Moser
Foilsithe / Cruthaithe 2023Artigo -
11
Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis de réir Uwe Kornak, Ansgar Schulz, W Friedrich, Siegfried Uhlhaas, B Kremens, Thomas Voït, Carola Hasan, U. Bode, Thomas J. Jentsch, Christian Kubisch
Foilsithe / Cruthaithe 2000Artigo -
12
Cholesterol metabolism is a potential therapeutic target in Duchenne muscular dystrophy de réir Fatima Amor, Ai Vu Hong, Guillaume Corre, Mathilde Sanson, Laurence Suel, Stéphanie Blaie, Laurent Servais, Thomas Voit, Isabelle Richard, David Israeli
Foilsithe / Cruthaithe 2021Artigo -
13
Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines de réir Matthew Thorley, Stéphanie Duguez, Emilia Maria Cristina Mazza, Sara Valsoni, Anne Bigot, Kamel Mamchaoui, Brennan Harmon, Thomas Voït, Vincent Mouly, William Duddy
Foilsithe / Cruthaithe 2016Artigo -
14
Efficacy of Fasting in Type 1 and Type 2 Diabetes Mellitus: A Narrative Review de réir Daniel Herz, Sandra Haupt, Rebecca T. Zimmer, Nadine Wachsmuth, Janis Schierbauer, Paul Zimmermann, Thomas Voït, Ulrike Thurm, Kayvan Khoramipour, Siân Rilstone, Othmar Moser
Foilsithe / Cruthaithe 2023Revisão -
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 de réir F. Pons, N Augier, Jocelyne Léger, Aude Robert, F.M.S. Tomé, Michel Fardeau, Thomas Voit, L. V. B. Nicholson, Dominique Mornet, J. Léger
Foilsithe / Cruthaithe 1991Artigo -
16
A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment de réir Anne‐Gaëlle Le Moing, A. Seferian, A. Moraux, M. Annoussamy, Éric Dorveaux, E. Gasnier, Jean‐Yves Hogrel, Thomas Voit, David Vissière, Laurent Servais
Foilsithe / Cruthaithe 2016Artigo -
17
Manual segmentation of individual muscles of the quadriceps femoris using MRI: A reappraisal de réir Yoann Barnouin, Gillian Butler‐Browne, Thomas Voit, David Reversat, Noura Azzabou, Gaëlle Leroux, Anthony Béhin, Jamie S. McPhee, Pierre G. Carlier, Jean‐Yves Hogrel
Foilsithe / Cruthaithe 2013Artigo -
18
Serum Profiling Identifies Novel Muscle miRNA and Cardiomyopathy-Related miRNA Biomarkers in Golden Retriever Muscular Dystrophy Dogs and Duchenne Muscular Dystrophy Patients de réir Laurence Jeanson-Leh, Julie Lameth, Soraya Krimi, Julien Buisset, Fatima Amor, Caroline Le Guiner, Inès Barthélémy, Laurent Servais, Stéphane Blot, Thomas Voit, David Israeli
Foilsithe / Cruthaithe 2014Artigo -
19
Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy de réir Phillipa J. Lamont, B. Udd, Francis Mastaglia, Marjolein Visser, Peter Hedera, Thomas Voït, Leslie Bridges, V. Fabian, Annemieke J.M. Rozemüller, Nigel G. Laing
Foilsithe / Cruthaithe 2005Artigo -
20
A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model de réir Maria Grazia Biferi, Mathilde Cohen-Tannoudji, Ambra Cappelletto, Benoit Giroux, Marianne Roda, Stéphanie Astord, Thibaut Marais, Corinne Bos, Thomas Voit, Arnaud Ferry, Martine Barkats
Foilsithe / Cruthaithe 2017Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Biology
Genetics
Internal medicine
Gene
Duchenne muscular dystrophy
Muscular dystrophy
Cell biology
Mutation
Pathology
Physical therapy
Dystrophin
Endocrinology
Biochemistry
Phenotype
Clinical trial
Disease
Pediatrics
Physical medicine and rehabilitation
Skeletal muscle
Laminin
Missense mutation
Myocyte
Bioinformatics
Cell
Computer science
Congenital muscular dystrophy
Dystroglycan
Exon
Genetic enhancement