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Accès maniaque : mode de révélation exceptionnel d’une maladie de Wilson
La Revue de Médecine Interne, 2017Introduction La maladie de Wilson (MW) ou degenerescence hepatolenticulaire progressive est une affection genetique, autosomique recessive. Il s’agit d’une toxicose cuprique caracterisee par une accumulation tissulaire de cuivre libre essentiellement dans le foie, le cerveau et l’œil.
A. Kefi +3 more
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De la schizophrénie à la maladie de Wilson*
The Canadian Journal of Psychiatry, 1992An 18 year-old male first presented a clinical picture of acute psychosis with two reccurences at ages 22 and 23. The diagnosis made at that time was paranoid schizophrenia. Twelve years after his first psychiatric hospitalization, it was discovered that he was suffering from Wilson's disease.
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Topological materials discovery from crystal symmetry
Nature Reviews Materials, 2021Benjamin J Wieder +2 more
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Copper homeostasis and cuproptosis in health and disease
Signal Transduction and Targeted Therapy, 2022Junxia Min, Fudi Wang
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Étude de l’observance médicamenteuse dans la maladie de Wilson
Revue Neurologique, 2022Élodie Jacquelet +3 more
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Maladie de Wilson : errance programmée ?
Revue Médicale Suisse, 2013Michel Bersier +2 more
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Maladie de Wilson : actualités et collaborations
Revue Neurologique, 2012F. Woimant +6 more
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