Ngā hua rapu kaituhi

1

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

I whakaputaina 2007

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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2

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

I whakaputaina 1992

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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3

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

I whakaputaina 2003

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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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 mā Anne-Charlotte Marsollier, Lukasz Ciszewski, Virginie Mariot, Linda Popplewell, Thomas Voit, George Dickson, Julie Dumonceaux

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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5

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

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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6

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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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7

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

I whakaputaina 2000

Whiwhi kuputuhi katoa
Artigo

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8

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

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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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... mā Eugenio Mercuri, Anna Mayhew, Francesco Muntoni, Sonia Messina, Volker Straub, G J van Ommen, Thomas Voit, Enrico Bertini, Kate Bushby

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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10

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

I whakaputaina 2023

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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11

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

I whakaputaina 2000

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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12

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

I whakaputaina 2021

Whiwhi kuputuhi katoa
Artigo

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13

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

I whakaputaina 2016

Whiwhi kuputuhi katoa
Artigo

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14

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

I whakaputaina 2023

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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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 mā F. Pons, N Augier, Jocelyne Léger, Aude Robert, F.M.S. Tomé, Michel Fardeau, Thomas Voit, L. V. B. Nicholson, Dominique Mornet, J. Léger

I whakaputaina 1991

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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16

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

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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17

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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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18

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

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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19

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

I whakaputaina 2005

Whiwhi kuputuhi katoa
Artigo

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20

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

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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Ngā hua rapu - Thomas Voit

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

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

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

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

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

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

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

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

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

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

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

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

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

Ngā utauta rapu:

Ngā marau whai pānga

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