Search Results - "Hogrel, Jean‐Yves"

Grip strength measured by high precision dynamometry in healthy subjects from 5 to 80 years by Hogrel, Jean-Yves

“…Grip strength is a variable which may be important to measure and follow in various populations. A new dynamometer with high accuracy and sensitivity has…”
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Still seeking the holy grail of outcome measures in inclusion body myositis by Hogrel, Jean-Yves

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Assessment of the upper limb function, strength, and mobility in treatment‐naive children with spinal muscular atrophy Types 2 and 3 by Milev, Evelin, Selby, Victoria, Wolfe, Amy, Rohwer, Annemarie, Tillmann, Ricarda, Ramsey, Danielle, Iodice, Mario, Hogrel, Jean‐Yves, Baranello, Giovanni, Scoto, Mariacristina, Muntoni, Francesco

“…Introduction/Aims Current upper limb assessments in pediatric spinal muscular atrophy (SMA) may not adequately capture change with disease progression. Our aim…”
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Non-invasive assessment of muscle stiffness in patients with duchenne muscular dystrophy by Lacourpaille, Lilian, Hug, François, Guével, Arnaud, Péréon, Yann, Magot, Armelle, Hogrel, Jean-Yves, Nordez, Antoine

“…Introduction: Assessment of muscle mechanical properties may provide clinically valuable information for follow‐up of patients with Duchenne muscular dystrophy…”
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Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy by Le Guiner, Caroline, Servais, Laurent, Montus, Marie, Larcher, Thibaut, Fraysse, Bodvaël, Moullec, Sophie, Allais, Marine, François, Virginie, Dutilleul, Maeva, Malerba, Alberto, Koo, Taeyoung, Thibaut, Jean-Laurent, Matot, Béatrice, Devaux, Marie, Le Duff, Johanne, Deschamps, Jack-Yves, Barthelemy, Inès, Blot, Stéphane, Testault, Isabelle, Wahbi, Karim, Ederhy, Stéphane, Martin, Samia, Veron, Philippe, Georger, Christophe, Athanasopoulos, Takis, Masurier, Carole, Mingozzi, Federico, Carlier, Pierre, Gjata, Bernard, Hogrel, Jean-Yves, Adjali, Oumeya, Mavilio, Fulvio, Voit, Thomas, Moullier, Philippe, Dickson, George

“…Duchenne muscular dystrophy (DMD) is an incurable X-linked muscle-wasting disease caused by mutations in the dystrophin gene. Gene therapy using highly…”
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Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA study by Chabanon, Aurélie, Seferian, Andreea Mihaela, Daron, Aurore, Péréon, Yann, Cances, Claude, Vuillerot, Carole, De Waele, Liesbeth, Cuisset, Jean-Marie, Laugel, Vincent, Schara, Ulrike, Gidaro, Teresa, Gilabert, Stéphanie, Hogrel, Jean-Yves, Baudin, Pierre-Yves, Carlier, Pierre, Fournier, Emmanuel, Lowes, Linda Pax, Hellbach, Nicole, Seabrook, Timothy, Toledano, Elie, Annoussamy, Mélanie, Servais, Laurent

“…Spinal muscular atrophy (SMA) is a monogenic disorder caused by loss of function mutations in the survival motor neuron 1 gene, which results in a broad range…”
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International clinimetric evaluation of the MG-QOL15, resulting in slight revision and subsequent validation of the MG-QOL15r by Burns, Ted M., Sadjadi, Reza, Utsugisawa, Kimiaki, Gwathmey, Kelly G., Joshi, Amruta, Jones, Sarah, Bril, Vera, Barnett, Carolina, Guptill, Jeffrey T., Sanders, Donald B., Hobson-Webb, Lisa, Juel, Vern C., Massey, Janice, Gable, Karissa L, Silvestri, Nicholas J., Wolfe, Gil, Cutter, Gary, Nagane, Yuriko, Murai, Hiroyuki, Masuda, Masayuki, Farrugia, Maria Elena, Carmichael, Caroline, Birnbaum, Simone, Hogrel, Jean-Yves, Nafissi, Shahriar, Fatehi, Farzad, Ou, Changyi, Liu, Weibin, Conaway, Mark

“…ABSTRACT Introduction: The MG‐QOL15 is a validated, health‐related quality of life (HRQOL) measure for myasthenia gravis (MG). Widespread use of the scale gave…”
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Genotype‐related respiratory progression in Duchenne muscular dystrophy—A multicenter international study by Trucco, Federica, Ridout, Deborah, Domingos, Joana, Maresh, Kate, Chesshyre, Mary, Munot, Pinki, Sarkozy, Anna, Robb, Stephanie, Quinlivan, Rosaline, Riley, Mollie, Wallis, Colin, Chan, Elaine, Abel, Francois, De Lucia, Silvana, Hogrel, Jean‐Yves, Niks, Erik H., Groot, Imelda, Servais, Laurent, Straub, Volker, Ricotti, Valeria, Manzur, Adnan, Muntoni, Francesco

“…Introduction/Aims Mutations amenable to skipping of specific exons have been associated with different motor progression in Duchenne muscular dystrophy (DMD)…”
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Hyperammonaemia following exercise may also reveal PGK1 deficiency by Hogrel, Jean-Yves, Ledoux, Isabelle, Béhin, Anthony

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Coupling between skeletal muscle fiber size and capillarization is maintained during healthy aging by Barnouin, Yoann, McPhee, Jamie S., Butler‐Browne, Gillian, Bosutti, Alessandra, De Vito, Giuseppe, Jones, David A., Narici, Marco, Behin, Anthony, Hogrel, Jean‐Yves, Degens, Hans

“…Background As muscle capillarization is related to the oxidative capacity of the muscle and the size of muscle fibres, capillary rarefaction may contribute to…”
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Ultrafast ultrasound coupled with cervical magnetic stimulation for non‐invasive and non‐volitional assessment of diaphragm contractility by Poulard, Thomas, Dres, Martin, Niérat, Marie‐Cécile, Rivals, Isabelle, Hogrel, Jean‐Yves, Similowski, Thomas, Gennisson, Jean‐Luc, Bachasson, Damien

“…Key points  Twitch transdiaphragmatic pressure elicited by cervical magnetic stimulation of the phrenic nerves is a fully non‐volitional method for assessing…”
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NMR based biomarkers to study age-related changes in the human quadriceps by Azzabou, Noura, Hogrel, Jean-Yves, Carlier, Pierre G.

“…Age-related sarcopenia is a major health issue. To improve elderly person quality of life, it is important to characterize age-associated structural changes…”
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Assessment of maximal handgrip strength: how many attempts are needed? by Reijnierse, Esmee M., Jong, Nynke, Trappenburg, Marijke C., Blauw, Gerard Jan, Butler‐Browne, Gillian, Gapeyeva, Helena, Hogrel, Jean‐Yves, McPhee, Jamie S., Narici, Marco V., Sipilä, Sarianna, Stenroth, Lauri, Lummel, Rob C., Pijnappels, Mirjam, Meskers, Carel G.M., Maier, Andrea B.

“…Background Handgrip strength (HGS) is used to identify individuals with low muscle strength (dynapenia). The influence of the number of attempts on maximal HGS…”
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Effect of sirolimus on muscle in inclusion body myositis observed with magnetic resonance imaging and spectroscopy by Reyngoudt, Harmen, Baudin, Pierre‐Yves, Caldas de Almeida Araújo, Ericky, Bachasson, Damien, Boisserie, Jean‐Marc, Mariampillai, Kubéraka, Annoussamy, Mélanie, Allenbach, Yves, Hogrel, Jean‐Yves, Carlier, Pierre G., Marty, Benjamin, Benveniste, Olivier

“…Background Finding sensitive clinical outcome measures has become crucial in natural history studies and therapeutic trials of neuromuscular disorders. Here,…”
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Systemic AAV8-Mediated Gene Therapy Drives Whole-Body Correction of Myotubular Myopathy in Dogs by Mack, David L., Poulard, Karine, Goddard, Melissa A., Latournerie, Virginie, Snyder, Jessica M., Grange, Robert W., Elverman, Matthew R., Denard, Jérôme, Veron, Philippe, Buscara, Laurine, Le Bec, Christine, Hogrel, Jean-Yves, Brezovec, Annie G., Meng, Hui, Yang, Lin, Liu, Fujun, O’Callaghan, Michael, Gopal, Nikhil, Kelly, Valerie E., Smith, Barbara K., Strande, Jennifer L., Mavilio, Fulvio, Beggs, Alan H., Mingozzi, Federico, Lawlor, Michael W., Buj-Bello, Ana, Childers, Martin K.

“…X-linked myotubular myopathy (XLMTM) results from MTM1 gene mutations and myotubularin deficiency. Most XLMTM patients develop severe muscle weakness leading…”
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Manual segmentation of individual muscles of the quadriceps femoris using MRI: A reappraisal by Barnouin, Yoann, Butler-Browne, Gillian, Voit, Thomas, Reversat, David, Azzabou, Noura, Leroux, Gaëlle, Behin, Anthony, McPhee, Jamie S., Carlier, Pierre G., Hogrel, Jean-Yves

“…Purpose To propose a manual segmentation method for individual quadriceps femoris (QF) muscles and to test its reliability for muscle volume estimation…”
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Reply to ‘Letter to the editor: is maximal diaphragm tissue velocity suited for the assessment of diaphragm contractility?’ by Poulard, Thomas, Dres, Martin, Niérat, Marie‐Cécile, Rivals, Isabelle, Hogrel, Jean‐Yves, Similowski, Thomas, Gennisson, Jean‐Luc, Bachasson, Damien

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Ultrasound shear wave elastography for assessing diaphragm function in mechanically ventilated patients: a breath-by-breath analysis by Fossé, Quentin, Poulard, Thomas, Niérat, Marie-Cécile, Virolle, Sara, Morawiec, Elise, Hogrel, Jean-Yves, Similowski, Thomas, Demoule, Alexandre, Gennisson, Jean-Luc, Bachasson, Damien, Dres, Martin

“…Abstract Background Diaphragm dysfunction is highly prevalent in mechanically ventilated patients. Recent work showed that changes in diaphragm shear modulus…”
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Natural history of Type 2 and 3 spinal muscular atrophy: 2‐year NatHis‐SMA study by Annoussamy, Mélanie, Seferian, Andreea M., Daron, Aurore, Péréon, Yann, Cances, Claude, Vuillerot, Carole, De Waele, Liesbeth, Laugel, Vincent, Schara, Ulrike, Gidaro, Teresa, Lilien, Charlotte, Hogrel, Jean‐Yves, Carlier, Pierre, Fournier, Emmanuel, Lowes, Linda, Gorni, Ksenija, Ly‐Le Moal, Myriam, Hellbach, Nicole, Seabrook, Timothy, Czech, Christian, Hermosilla, Ricardo, Servais, Laurent

“…Objective To characterize the natural history of spinal muscular atrophy (SMA) over 24 months using innovative measures such as wearable devices, and to…”
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Quantitative muscle MRI as an assessment tool for monitoring disease progression in LGMD2I: a multicentre longitudinal study by Willis, Tracey A, Hollingsworth, Kieren G, Coombs, Anna, Sveen, Marie-Louise, Andersen, Søren, Stojkovic, Tanya, Eagle, Michelle, Mayhew, Anna, de Sousa, Paulo L, Dewar, Liz, Morrow, Jasper M, Sinclair, Christopher D J, Thornton, John S, Bushby, Kate, Lochmüller, Hanns, Hanna, Michael G, Hogrel, Jean-Yves, Carlier, Pierre G, Vissing, John, Straub, Volker

“…Outcome measures for clinical trials in neuromuscular diseases are typically based on physical assessments which are dependent on patient effort, combine the…”
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