Motor complications and postural abnormalities interplay in Parkinson's disease
Margherita Fabbri, Aymeric Lanore, Nathalie Bertille, Jean-Christophe Corvol et autres
fr, us (code pays fourni par la source)
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
Margherita Fabbri, Aymeric Lanore, Nathalie Bertille, Jean-Christophe Corvol et autres
fr, us (code pays fourni par la source)
Margherita Fabbri, Natalia del Campo, Wassilios G. Meissner, Vanessa Rousseau et autres
OBJECTIVE: The objective of this study was to characterize changes in candidate biomarkers in early multiple system atrophy (MSA) and identify baseline predictors of faster progression. METHODS: This 1-year, multicenter, prospective study assessed clinical, neuroimaging (3T-magnetic resonance imaging [MRI], dopamine transporter single-photon …
fr, gb (code pays fourni par la source)
Clément Desjardins, Paulo André Dias Bastos, Aymeric Lanore, Christine Brefel‐Courbon et autres
BACKGROUND: Impulse control disorders (ICD) are common non-motor complications in Parkinson's disease (PD), particularly in patients receiving oral dopamine agonists (DA). Continuous subcutaneous apomorphine infusion (CSAI) is a device-aided therapy for advanced PD, but its effects on ICD remain underexplored in real-world …
fr (code pays fourni par la source)
Thomas Ollivier, David Devos, Grégory Kuchcinski, Luc Defebvre et autres
There is a distinct lack of consensus on the most effective treatments for neurodegeneration with brain iron accumulation. This is due to the rarity of the disease, its phenotypic variability, and the multiplicity of pathophysiological mechanisms. Our team has already proposed the …
fr (code pays fourni par la source)
fr (code pays fourni par la source)
Felix Marchand, Anne-Sophie Blaise, Luc Defebvre, Émeline Cailliau et autres
BACKGROUND: Progressive supranuclear palsy (PSP) is a rare neurodegenerative disease with diverse clinical phenotypes, prompting the development of new diagnostic criteria known as the MDS-PSP classification. However, little is known about the prognostic value of this classification in order to better stratify …
fr (code pays fourni par la source)
Özge Gönül Öner, Valérie Fraix, Veronique Bourg, Luc Defebvre et autres
Background In pediatric age, the PRKN mutation is reported as one of the most common genetic causes of Parkinson's disease. However, detailed clinical data on PRKN patients with pediatric onset are scarce. Objective To describe clinical characteristics, disease progression, and management of …
fr (code pays fourni par la source)
Ludovic Dupont, Luc Defebvre, Jean‐Baptiste Davion, Arnaud Delval et autres
BACKGROUND: Demyelinating polyneuropathies affect posture and can be either hereditary, as in Charcot-Marie-Tooth type 1A (CMT1A), or autoimmune, as in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Clinical differentiation between these two neuropathies can be challenging and biomarkers are lacking. No comparative analysis of …
fr (code pays fourni par la source)
fr (code pays fourni par la source)
Morgane Gérard, Madli Bayot, Kathy Dujardin, Luc Defebvre et autres
fr (code pays fourni par la source)
Felix Marchand, Romain Viard, Luc Defebvre, David Devos et autres
fr (code pays fourni par la source)
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