celine tard|Motor and respiratory decline in patients with late : 2024-10-22 ∗Correspondence to: Celine Tard, MD, Neurologie et Pathologie´ du Mouvement, Hopital Salengro, Centre Hospitalier Universitaire,ˆ F-59037 Lille Cedex, France. Draugiem.lv mobilā versija ļaus Tev vienmēr būt pieskāriena attālumā no Taviem draugiem, sūtīt viņiem vēstules, skatīties galerijas un sekot jaunumiem profilos. Ērti, vienkārši un bez maksas.
0 · Specific Attentional Disorders and Freezing of Gait in
1 · Regulatory Role of Natural Killer T Cells in Diabetes
2 · Real‐life effectiveness 1 year after switching to avalglucosidase
3 · Motor and respiratory decline in patients with late
4 · Freezing/festination during motor tasks in early‐stage
5 · Factors impacting performance on the 6
6 · Bulbar muscle impairment in patients with late onset Pompe
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celine tard*******Open Access. Real-life effectiveness 1 year after switching to avalglucosidase alfa in late-onset Pompe disease patients worsening on alglucosidase alfa therapy: A .Céline Tard, Department of Neurology, Salengro Hospital, University of Lille .
Céline Tard, Department of Neurology, Salengro Hospital, University of Lille Hospital, Emile Laine Street, 59037 Lille cedex, France. Email: [email protected]
Late onset Pompe disease (LOPD) is a rare neuromuscular disorder caused by a deficit in acid alpha-glucosidase. Macroglossia and swallowing disorders have .∗Correspondence to: Celine Tard, MD, Neurologie et Pathologie´ du Mouvement, Hopital Salengro, Centre Hospitalier Universitaire,ˆ F-59037 Lille Cedex, France.
Growing evidence points to a role of immune system in glucose intolerance and type 2 diabetes. iNKT cells are resident cells of adipose tissue and their local and systemic .
Background. Parkinsonian patients have a tendency to speed up during repetitive motor tasks (festination) and to experience sudden motor blocks (freezing). In this article, we prospectively studied .Abstract. Introduction/aims: Pompe disease is a progressive myopathy that combines motor, respiratory, and cardiac impairments. The 6-min walk test is the gold standard for .Motor and respiratory decline in patients with late Open Access. Real-life effectiveness 1 year after switching to avalglucosidase alfa in late-onset Pompe disease patients worsening on alglucosidase alfa therapy: A French cohort study. Céline Tard, Françoise Bouhour, Maud Michaud, Stephane Beltran, Maxime Fournier, Florence Demurger, Emmeline Lagrange, Sylvain Nollet, Sabrina .
Céline Tard, Department of Neurology, Salengro Hospital, University of Lille Hospital, Emile Laine Street, 59037 Lille cedex, France. Email: [email protected]
Late onset Pompe disease (LOPD) is a rare neuromuscular disorder caused by a deficit in acid alpha-glucosidase. Macroglossia and swallowing disorders have already been reported, but no study has focused yet on its frequency and functional impact on patients' daily life.
celine tard∗Correspondence to: Celine Tard, MD, Neurologie et Pathologie´ du Mouvement, Hopital Salengro, Centre Hospitalier Universitaire,ˆ F-59037 Lille Cedex, France.Growing evidence points to a role of immune system in glucose intolerance and type 2 diabetes. iNKT cells are resident cells of adipose tissue and their local and systemic frequencies are reduced in obese patients, suggesting their involvement in local and systemic inflammation during obesity.
Background. Parkinsonian patients have a tendency to speed up during repetitive motor tasks (festination) and to experience sudden motor blocks (freezing). In this article, we prospectively studied the appearance and progression of these phenomena in 30 early-stage PD patients.celine tard Motor and respiratory decline in patients with late Abstract. Introduction/aims: Pompe disease is a progressive myopathy that combines motor, respiratory, and cardiac impairments. The 6-min walk test is the gold standard for assessing disease severity at the motor level.
Mucosal-associated invariant T cells (MAIT cells) are innate-like T-cells that recognize derivatives of precursors of bacterial riboflavin presented by the major histocompatibility complex (MHC) class I-related molecule MR1. Since T1D is associated with modification of the gut microbiota, we investigated MAIT cells in this pathology.
no code implementations • 25 Jan 2022 • Vincent Huin, Giulia Coarelli, Clément Guemy, Susana Boluda, Rabab Debs, Fanny Mochel, Tanya Stojkovic, David Grabli, Thierry Maisonobe, Bertrand Gaymard, Timothée Lenglet, Céline Tard, Jean-Baptiste Davion, Bernard Sablonnière, Marie-Lorraine Monin, Claire Ewenczyk, Karine Viala, Perrine . Céline Tard received a grant from Santelys and has received various honoraria for lectures on neuromuscular disorders. Luc Defebvre served on several Scientific Advisory Boards for Abbvie and Zambon. Open Access. Real-life effectiveness 1 year after switching to avalglucosidase alfa in late-onset Pompe disease patients worsening on alglucosidase alfa therapy: A French cohort study. Céline Tard, Françoise Bouhour, Maud Michaud, Stephane Beltran, Maxime Fournier, Florence Demurger, Emmeline Lagrange, Sylvain Nollet, Sabrina . Céline Tard, Department of Neurology, Salengro Hospital, University of Lille Hospital, Emile Laine Street, 59037 Lille cedex, France. Email: [email protected] Late onset Pompe disease (LOPD) is a rare neuromuscular disorder caused by a deficit in acid alpha-glucosidase. Macroglossia and swallowing disorders have already been reported, but no study has focused yet on its frequency and functional impact on patients' daily life.∗Correspondence to: Celine Tard, MD, Neurologie et Pathologie´ du Mouvement, Hopital Salengro, Centre Hospitalier Universitaire,ˆ F-59037 Lille Cedex, France.Growing evidence points to a role of immune system in glucose intolerance and type 2 diabetes. iNKT cells are resident cells of adipose tissue and their local and systemic frequencies are reduced in obese patients, suggesting their involvement in local and systemic inflammation during obesity. Background. Parkinsonian patients have a tendency to speed up during repetitive motor tasks (festination) and to experience sudden motor blocks (freezing). In this article, we prospectively studied the appearance and progression of these phenomena in 30 early-stage PD patients.
Abstract. Introduction/aims: Pompe disease is a progressive myopathy that combines motor, respiratory, and cardiac impairments. The 6-min walk test is the gold standard for assessing disease severity at the motor level.
Mucosal-associated invariant T cells (MAIT cells) are innate-like T-cells that recognize derivatives of precursors of bacterial riboflavin presented by the major histocompatibility complex (MHC) class I-related molecule MR1. Since T1D is associated with modification of the gut microbiota, we investigated MAIT cells in this pathology.
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celine tard|Motor and respiratory decline in patients with late