Fahimi, Dariush

A mouse model for Zellweger syndrome

Baes, M., Gressens, P., Baumgart, E., Carmeliet, P., Casteels, M., Fransen, M., Evrard, P., Fahimi, D., Declercq, P. E., Collen, D., et al. (1997) · Nature Genetics

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 275

Absence of peroxisomes in mouse hepatocytes causes mitochondrial and ER abnormalities†

Dirkx, R., Vanhorebeek, I., Martens, K., Schad, A., Grabenbauer, M., Fahimi, D., Declercq, P., Van Veldhoven, P. P., & Baes, M. (2005) · Hepatology

Metabolism and Genetic DisordersMitochondrial Function and Pathology

Cited by 174

Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissues

Janssen, A., Gressens, P., Grabenbauer, M., Baumgart, E., Schad, A., Vanhorebeek, I., Brouwers, A., Declercq, P. E., Fahimi, D., Evrard, P., et al. (2003) · The Journal of Neuroscience

Metabolism and Genetic DisordersNeurogenesis and neuroplasticity mechanisms

Cited by 65