Khalid H. El Hachimi
Paris, France
Last Updated: 09/26/2026
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Found 15 publications
Golgi localization of SARS-CoV-2 spike protein and interaction with furin in cerebral COVID-19 microangiopathy: a clue to the central nervous system involvement?
Journal: Free neuropathology
Published: January 04, 2023
CNS-associated T-lymphocytes in a mouse model of Hereditary Spastic Paraplegia type 11 (SPG11) are therapeutic targets for established immunomodulators.
Journal: Experimental neurology
Published: March 30, 2022
Alterations of Neuronal Lysosomes in Alzheimer's Disease and in APPxPS1-KI Mice.
Journal: Journal of Alzheimer's disease : JAD
Published: March 11, 2022
Implication of folate deficiency in CYP2U1 loss of function.
Journal: The Journal of experimental medicine
Published: April 20, 2021
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia.
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia.
Journal: Brain : a journal of neurology
Published: March 12, 2021
Progressive ataxia of Charolais cattle highlights a role of KIF1C in sustainable myelination.
Journal: PLoS genetics
Published: March 29, 2018
Evidence for altered dendritic spine compartmentalization in Alzheimer's disease and functional effects in a mouse model.
Journal: Acta neuropathologica
Published: February 13, 2018
Loss of spatacsin function alters lysosomal lipid clearance leading to upper and lower motor neuron degeneration.
Journal: Neurobiology of disease
Published: October 26, 2016
Lentiviral vector-mediated overexpression of mutant ataxin-7 recapitulates SCA7 pathology and promotes accumulation of the FUS/TLS and MBNL1 RNA-binding proteins.
Journal: Molecular neurodegeneration
Published: December 12, 2015
Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions.
Journal: Brain : a journal of neurology
Published: October 27, 2015
Last Updated: 09/26/2026