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authFullName_s : Helge Amthor

Asymmetric muscle weakness due to ACTA1 mosaic mutations

Xaviére Lornage , Susana Quijano-Roy , Robert Yves Carlier , Nicole Monnier , Jean François Deleuze et al.
Neurology, 2020, 95 (24), pp.e3406-e3411. ⟨10.1212/WNL.0000000000010947⟩
Journal articles hal-03109127v1
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Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort

Susana Quijano-Roy , Jana Haberlova , Claudia Castiglioni , John Vissing , Francina Munell et al.
Journal of Neurology, In press, ⟨10.1007/s00415-021-10806-0⟩
Journal articles hal-03359688v1
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ActRIIB blockade increases force‐generating capacity and preserves energy supply in exercising mdx mouse muscle in vivo

Nelly Béchir , Emilie Pecchi , Christophe Vilmen , Yann Le Fur , Helge Amthor et al.
FASEB Journal, 2016, 30 (10), pp.3551-3562. ⟨10.1096/fj.201600271RR⟩
Journal articles hal-03548287v1

ActRIIB blockade increases force-generating capacity and preserves energy supply in exercising mdx mouse muscle in vivo

Nelly Béchir , Emilie Pecchi , Christophe Vilmen , Yann Le Fur , Helge Amthor et al.
FASEB Journal, 2016, 30 (10), pp.3551--3562. ⟨10.1096/fj.201600271RR⟩
Journal articles hal-01425491v1

240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25-27 January 2019, Hoofddorp, The Netherlands

Jennifer Morgan , Gillian Butler-Browne , Francesco Muntoni , Ketan Patel , Helge Amthor et al.
Neuromuscular Disorders, 2019, 29 (9), pp.704-715. ⟨10.1016/j.nmd.2019.07.003⟩
Journal articles hal-03201551v1
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Determinants of diaphragm inspiratory motion, diaphragm thickening, and its performance for predicting respiratory restrictive pattern in Duchenne muscular dystrophy

Abdallah Fayssoil , Lee S Nguyen , Tanya Stojkovic , Helene Prigent , Robert Carlier et al.
Muscle & nerve. Supplement., 2022, 65 (1), pp.89-95. ⟨10.1002/mus.27432⟩
Journal articles hal-03521139v1

BMP signaling regulates satellite cell-dependent postnatal muscle growth

Amalia Stantzou , Elija Schirwis , Sandra Swist , Sonia Alonso-Martin , Ioanna Polydorou et al.
Development (Cambridge, England), 2017, 144 (15), pp.2737-2747. ⟨10.1242/dev.144089⟩
Journal articles hal-02407976v1
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The effect of constitutive inactivation of the myostatin gene on the gain in muscle strength during postnatal growth in two murine models

Amalia Stantzou , Vanessa Ueberschlag-Pitiot , Rémi Thomasson , Denis Furling , Anne Bonnieu et al.
Muscle & Nerve, 2016, 55 (2), pp.254-261. ⟨10.1002/mus.25220⟩
Journal articles hal-01346093v1

Myostatin is a key mediator between energy metabolism and endurance capacity of skeletal muscle

Etienne Mouisel , Karima Relizani , Laurence Mille-Hamard , Raphael Denis , Christophe Hourde et al.
AJP - Regulatory, Integrative and Comparative Physiology, 2014, 307 (4), pp.R444-R454. ⟨10.1152/ajpregu.00377.2013⟩
Journal articles hal-01545449v1

Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.

Takuro Arimura , Anne Helbling-Leclerc , Catherine Massart , Shaida Varnous , Florence Niel et al.
Human Molecular Genetics, 2005, 14 (1), pp.155-69. ⟨10.1093/hmg/ddi017⟩
Journal articles hal-00165763v1
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Live-imaging of revertant and therapeutically restored dystrophin in the DmdEGFP-mdx mouse model for Duchenne muscular dystrophy

Mina V. Petkova , Amalia Stantzou , A. Morin , O. Petrova , Susanne Morales-Gonzalez et al.
Neuropathology and Applied Neurobiology, 2020, 46 (6), pp.602-614. ⟨10.1111/nan.12639⟩
Journal articles hal-02984274v2
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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita

Annie Laquerriere , Dana Jaber , Emanuela Abiusi , Jérome Maluenda , Dan Mejlachowicz et al.
Journal of Medical Genetics, 2021, 59 (6), ⟨10.1136/jmedgenet-2020-107595⟩
Journal articles hal-03708085v1
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Mitochondrial impairment induced by postnatal ActRIIB blockade does not alter function and energy status in exercising mouse glycolytic muscle in vivo

Nelly Béchir , Émilie Pecchi , Karima Relizani , Christophe Vilmen , Yann Le Fur et al.
AJP - Endocrinology and Metabolism, 2016, 310 (7), pp.E539-E549. ⟨10.1152/ajpendo.00370.2015⟩
Journal articles hal-03548290v1
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Association between prophylactic angiotensin-converting enzyme inhibitors and overall survival in Duchenne muscular dystrophy—analysis of registry data

Raphaël Porcher , Isabelle Desguerre , Helge Amthor , Brigitte Chabrol , Frédérique Audic et al.
European Heart Journal, 2021, ⟨10.1093/eurheartj/ehab054⟩
Journal articles hal-03179750v1

Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers

Aurélie Goyenvalle , Graziella Griffith , Arran Babbs , Samir El Andaloussi , Kariem Ezzat et al.
Nature Medicine, 2015, 21 (3), pp.270-275. ⟨10.1038/nm.3765⟩
Journal articles hal-02407968v1

SIX1 and SIX4 homeoproteins regulate PAX7+ progenitor cell properties during fetal epaxial myogenesis

Maud Wurmser , Nathalie Chaverot , Rouba Madani , Hiroshi Sakai , Elisa Negroni et al.
Development (Cambridge, England), 2020, pp.dev.185975. ⟨10.1242/dev.185975⟩
Journal articles hal-02905565v1

Un nouvel outil pour le traitement de la myopathie de Duchenne : les tricyclo-ADN

Aurélie Goyenvalle , Graziella Griffith , Aurélie Avril , Helge Amthor , Luis Garcia et al.
médecine/sciences, 2015, 31 (3), pp.253-256. ⟨10.1051/medsci/20153103009⟩
Journal articles hal-02407963v1