B. Namour

Homocysteine and methylenetetrahydrofolate reductase polymorphism in Alzheimer's disease

Jean-Luc Daval, Filippo Caraci, Raffaele Ferri, 2004, Neuroreport.

Genetic, epigenetic and genomic mechanisms of methionine dependency of cancer and tumor-initiating cells: What could we learn from folate and methionine cycles.

Youssef Siblini, A. Oussalah, B. Namour, 2020, Biochimie.

Methyl deficient diet aggravates experimental colitis in rats

L. Peyrin-Biroulet, B. Xia, A. Bressenot, 2011, Journal of cellular and molecular medicine.

Association of IL-1 RN*2 allele and methionine synthase 2756 AA genotype with dementia severity of sporadic Alzheimer’s disease

P. Bosco, R. Ferri, F. Caraci, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Genetic Determinants of Folate and Vitamin B12 Metabolism: A Common Pathway in Neural Tube Defect and Down Syndrome?

P. Bosco, C. Romano, M. Candito, 2003, Clinical chemistry and laboratory medicine.

[Molecular pharmacogenetics in hospital laboratories in France: current data and future prospects].

M. Loriot, P. Beaune, P. Marquet, 2007, Annales pharmaceutiques francaises.

Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans

P. Bosco, R. Guéant-Rodriguez, P. Gérard, 2003, Neuroscience Letters.