Publications of François Meyer
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See detailPathologies neuromotrices chroniques de l'enfant
DEPIERREUX, Frédérique ULiege; Meyer, François ULiege; Vogel, Lindsay ULiege

Scientific conference (2021, December 14)

Journée de formation divisée en 3 sessions; 1) Mouvements anormaux et grands syndromes moteurs: Aspects théoriques et phénoménologiques. 2) Aspects thérapeutiques en mouvements anormaux pédiatriques. 3 ... [more ▼]

Journée de formation divisée en 3 sessions; 1) Mouvements anormaux et grands syndromes moteurs: Aspects théoriques et phénoménologiques. 2) Aspects thérapeutiques en mouvements anormaux pédiatriques. 3) Analyse sémiologique de cas cliniques: exercices pratiques et vidéographiques. [less ▲]

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See detailLa maladie d’Alzheimer à l’ère des biomarqueurs : le point de vue du clinicien
Meyer, François ULiege

Scientific conference (2021, September 23)

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See detailSynaptic Modification in Subjective Cognitive Decline
Meyer, François ULiege

Scientific conference (2020, October 21)

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See detailIn vivo imaging of synaptic loss in Alzheimer’s disease with [18F]UCB-H Positron Emission Tomography
Bastin, Christine ULiege; Bahri, Mohamed Ali ULiege; Meyer, François ULiege et al

in European Journal of Nuclear Medicine and Molecular Imaging (2020), 47(2), 390-402

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See detailAdult hippocampus neurogenesis in healthy and Alzheimer subjects
Meyer, François ULiege

Scientific conference (2019)

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See detailCharacterization of a temporoparietal junction subtype of Alzheimer’s disease
Meyer, François ULiege; Wehenkel, Marie ULiege; Phillips, Christophe ULiege et al

in Human Brain Mapping (2019), 40

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See detailToward a biological definition of Alzheimer's disease
Meyer, François ULiege

Scientific conference (2018, December 01)

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See detailEnseignement postgradue des neurosciences Presentation de cas cliniques par les candidats spécialistes
Meyer, François ULiege

Scientific conference (2018, March 15)

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See detailVeillissement cognitif : Aspects médicaux
Meyer, François ULiege

Conference given outside the academic context (2017)

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See detailDystonie de type 12 : un diagnostic rare et difficile.
LEROY, Patricia ULiege; Meyer, François ULiege; Vaessen, S. et al

in Archives de Pédiatrie (2017), 24(7), 637-639

We report a case of dystonia 12, also called rapid-onset dystonia-parkinsonism, which occurred in a young 12-year-old boy. Type 12 dystonia is a genetic syndrome characterized by a pathogenic mutation on ... [more ▼]

We report a case of dystonia 12, also called rapid-onset dystonia-parkinsonism, which occurred in a young 12-year-old boy. Type 12 dystonia is a genetic syndrome characterized by a pathogenic mutation on ATP1A3 gene encoding the subunit alpha 3 of Na-K-ATPase protein, resulting in neuronal dysfunctions. It remains a rare syndrome with less than 100 cases described in the literature. Its atypical presentation and its rarity may lead to a wandering diagnosis, even in some cases to a conversion hysteria diagnosis. Today, unfortunately, there is no effective treatment. [less ▲]

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