K. El-Hachimi

发表

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.

A. Durr, C. Depienne, A. Brice, 2014, American journal of human genetics.

Alpha-synuclein accumulates in the brain of scrapie-affected sheep and goats.

K. El-Hachimi, K. Adjou, J. Deslys, 2007, Journal of comparative pathology.

KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations

G. Gyapay, S. Klebe, A. Durr, 2012, European Journal of Human Genetics.

Developmental Cell Death Is Enhanced in the Cerebral Cortex of Mice Lacking the Brain Vesicular Monoamine Transporter

P. Gaspar, C. Alvarez, E. Deneris, 2007, The Journal of Neuroscience.

Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.

G. Gyapay, A. Durr, F. Lamari, 2012, American journal of human genetics.

CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56

A. Durr, F. Rivier, G. Stevanin, 2018, Human mutation.

Diffuse senile plaques: amorphous or fibrous?

F. Tagliavini, K. El-Hachimi, L. Verga, 1995, American Journal of Pathology.

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.

A. Durr, C. Depienne, A. Brice, 2014, American journal of human genetics.

Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.

G. Gyapay, A. Durr, F. Lamari, 2012, American journal of human genetics.