Search Results - "Le Louër, Julien"

Global versus individual muscle segmentation to assess quantitative MRI-based fat fraction changes in neuromuscular diseases by Reyngoudt, Harmen, Marty, Benjamin, Boisserie, Jean-Marc, Le Louër, Julien, Koumako, Cedi, Baudin, Pierre-Yves, Wong, Brenda, Stojkovic, Tanya, Béhin, Anthony, Gidaro, Teresa, Allenbach, Yves, Benveniste, Olivier, Servais, Laurent, Carlier, Pierre G.

“…Objectives Magnetic resonance imaging (MRI) constitutes a powerful outcome measure in neuromuscular disorders, yet there is a broad diversity of approaches in…”
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Quantitative nuclear magnetic resonance imaging detects subclinical changes over 1 year in skeletal muscle of GNE myopathy by Gidaro, Teresa, Reyngoudt, Harmen, Le Louër, Julien, Behin, Anthony, Toumi, Ferial, Villeret, Melanie, Araujo, Ericky C. A., Baudin, Pierre-Yves, Marty, Benjamin, Annoussamy, Melanie, Hogrel, Jean-Yves, Carlier, Pierre G., Servais, Laurent

“…Background and objective To identify the most responsive and sensitive clinical outcome measures in GNE myopathy. Methods ClinBio-GNE is a natural history…”
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Three‐year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy by Reyngoudt, Harmen, Smith, Fiona E., Caldas de Almeida Araújo, Ericky, Wilson, Ian, Fernández‐Torrón, Roberto, James, Meredith K., Moore, Ursula R., Díaz‐Manera, Jordi, Marty, Benjamin, Azzabou, Noura, Gordish, Heather, Rufibach, Laura, Hodgson, Tim, Wallace, Dorothy, Ward, Louise, Boisserie, Jean‐Marc, Le Louër, Julien, Hilsden, Heather, Sutherland, Helen, Canal, Aurélie, Hogrel, Jean‐Yves, Jacobs, Marni, Stojkovic, Tanya, Bushby, Kate, Mayhew, Anna, Straub, Volker, Carlier, Pierre G., Blamire, Andrew M.

“…Background Natural history studies in neuromuscular disorders are vital to understand the disease evolution and to find sensitive outcome measures. We…”
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Upper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophy by Lilien, Charlotte, Reyngoudt, Harmen, Seferian, Andreea Mihaela, Gidaro, Teresa, Annoussamy, Mélanie, Chê, Virginie, Decostre, Valérie, Ledoux, Isabelle, Le Louër, Julien, Guemas, Eric, Muntoni, Francesco, Hogrel, Jean‐Yves, Carlier, Pierre Georges, Servais, Laurent

“…Objective To understand the natural disease upper limb progression over 3 years of ambulatory and non‐ambulatory patients with Duchenne muscular dystrophy…”
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MRI vastus lateralis fat fraction predicts loss of ambulation in Duchenne muscular dystrophy by Naarding, Karin J., Reyngoudt, Harmen, van Zwet, Erik W., Hooijmans, Melissa T., Tian, Cuixia, Rybalsky, Irina, Shellenbarger, Karen C., Le Louër, Julien, Wong, Brenda L., Carlier, Pierre G., Kan, Hermien E., Niks, Erik H.

“…OBJECTIVEWe studied the potential of quantitative MRI (qMRI) as a surrogate endpoint in Duchenne muscular dystrophy by assessing the additive predictive value…”
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Water-Fat Separation in MR Fingerprinting for Quantitative Monitoring of the Skeletal Muscle in Neuromuscular Disorders by Marty, Benjamin, Reyngoudt, Harmen, Boisserie, Jean-Marc, Le Louër, Julien, C. A. Araujo, Ericky, Fromes, Yves, Carlier, Pierre G.

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Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophy by Wary, Claire, Azzabou, Noura, Giraudeau, Céline, Le Louër, Julien, Montus, Marie, Voit, Thomas, Servais, Laurent, Carlier, Pierre

“…Quantitative NMRI and 31P NMRS indices are reported in the forearms of 24 patients with Duchenne muscular dystrophy (DMD) (6–18 years, 14 non‐ambulant)…”
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Relationship between markers of disease activity and progression in skeletal muscle of GNE myopathy patients using quantitative nuclear magnetic resonance imaging and (31)P nuclear magnetic resonance spectroscopy by Reyngoudt, Harmen, Marty, Benjamin, Caldas de Almeida Araújo, Ericky, Baudin, Pierre-Yves, Le Louër, Julien, Boisserie, Jean-Marc, Béhin, Anthony, Servais, Laurent, Gidaro, Teresa, Carlier, Pierre G.

“…BACKGROUND: Quantitative nuclear magnetic resonance imaging (NMRI) is an objective and precise outcome measure for evaluating disease progression in…”
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Relationship between markers of disease activity and progression in skeletal muscle of GNE myopathy patients using quantitative nuclear magnetic resonance imaging and 31 P nuclear magnetic resonance spectroscopy by Reyngoudt, Harmen, Marty, Benjamin, Caldas de Almeida Araújo, Ericky, Baudin, Pierre-Yves, Le Louër, Julien, Boisserie, Jean-Marc, Béhin, Anthony, Servais, Laurent, Gidaro, Teresa, Carlier, Pierre G

“…Quantitative nuclear magnetic resonance imaging (NMRI) is an objective and precise outcome measure for evaluating disease progression in neuromuscular…”
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Relationship between markers of disease activity and progression in skeletal muscle of GNE myopathy patients using quantitative nuclear magnetic resonance imaging and 31P nuclear magnetic resonance spectroscopy by Reyngoudt, Harmen, Marty, Benjamin, Caldas de Almeida Araújo, Ericky, Baudin, Pierre-Yves, Le Louër, Julien, Boisserie, Jean-Marc, Béhin, Anthony, Servais, Laurent, Gidaro, Teresa, Carlier, Pierre G.

“…BACKGROUNDQuantitative nuclear magnetic resonance imaging (NMRI) is an objective and precise outcome measure for evaluating disease progression in…”
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