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pro vyhledávání: '"Valentin Oger"'
Autor:
Emilie Audouard, Valentin Oger, Béatrix Meha, Nathalie Cartier, Caroline Sevin, Françoise Piguet
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder characterized by accumulation of sulfatides in both glial cells and neurons. MLD results from an inherited deficiency of arylsulfatase A (ARSA) and myelin degeneration in the central
Externí odkaz:
https://doaj.org/article/5c4e8a50d7044a1cb21a229a411d1dbf
Autor:
Pascale Chrétien, Chloé Bost, Lucie Salah, Marie Benaiteau, Valentin Oger, Elise Yazbeck, Catherine Adamsbaum, Kumaran Deiva, Celine Bellesme, Jérôme Honnorat, Hélène Maurey, Caroline Sevin
Publikováno v:
European Journal of Paediatric Neurology
European Journal of Paediatric Neurology, Elsevier, 2020, 26, pp.89-91. ⟨10.1016/j.ejpn.2020.03.002⟩
European Journal of Paediatric Neurology, Elsevier, 2020, 26, pp.89-91. ⟨10.1016/j.ejpn.2020.03.002⟩
Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is a rare recently defined antibody-mediated encephalitis. Meningo-encephalomyelitis presentation is frequent with lymphocytic pleiocytosis in the cerebro-spinal fluid and brain MRI cla