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Publications

Development of a cellular model to study the role of CR1 in Alzheimer's disease

Cardona F. et al, (2022), European Journal of Human Genetics

Evaluation of a novel variant in CR1 in patients with Alzheimer's disease

Szymanski J. et al, (2022), European Journal of Human Genetics

NKCC1 Deficiency in Forming Hippocampal Circuits Triggers Neurodevelopmental Disorder: Role of BDNF-TrkB Signalling.

Szymanski J. and Minichiello L., (2022), Brain Sci, 12

Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome.

Vázquez-Costa JF. et al, (2021), Front Mol Neurosci, 14

Interleukin 6 deficiency affects spontaneous activity of mice in age- and sex-dependent manner.

Aniszewska A. et al, (2014), Acta Neurobiol Exp (Wars), 74, 424 - 432

Include forthcoming?