Nonsynonymous Polymorphisms of Histamine-Metabolising Enzymes in Patients with Parkinson’s Disease

Author:

Agúndez José A. G.,Luengo Antonio,Herráez Oscar,Martínez Carmen,Alonso-Navarro Hortensia,Jiménez-Jiménez Félix Javier,García-Martín Elena

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology,Molecular Medicine

Reference55 articles.

1. Abbas, N., Lucking, C. B., Ricard, S., Durr, A., Bonifati, V., De Michele, G., Bouley, S., Vaughan, J. R., Gasser, T., Marconi, R., Broussolle, E., Brefel-Courbon, C., Harhangi, B. S., Oostra, B. A., Fabrizio, E., Bohme, G. A., Pradier, L., Wood, N. W., Filla, A., Meco, G., Denefle, P., Agid, Y., & Brice, A. (1999). A wide variety of mutations in the parkin gene are responsible for autosomal recessive Parkinsonism in Europe. French Parkinson’s Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson’s Disease. Human Molecular Genetics, 8, 567–574.

2. Abeliovich, A., & Flint Beal, M. (2006). Parkinsonism genes: Culprits and clues. Journal of Neurochemistry, 99, 1062–1072.

3. Agundez, J. A., Jimenez-Jimenez, F. J., Luengo, A., Bernal, M. L., Molina, J. A., Ayuso, L., Vazquez, A., Parra, J., Duarte, J., Coria F., et al. (1995). Association between the oxidative polymorphism and early onset of Parkinson’s disease. Clinical Pharmacology and Therapeutics, 57, 291–298.

4. Agundez, J. A., Jimenez-Jimenez F. J., Luengo A., Molina J. A., Orti-Pareja M., Vazquez A., Ramos F., Duarte J., Coria F., Ladero J. M., Alvarez-Cermeno J. C., & Benitez J. (1998). Slow allotypic variants of the NAT2 gene and susceptibility to early-onset Parkinson’s disease. Neurology, 51, 1587–1592.

5. Agundez, J. A., Rodriguez I., Olivera M., Ladero J. M., Garcia M. A., Ribera J. M., & Benitez J. (1997). CYP2D6, NAT2 and CYP2E1 genetic polymorphisms in nonagenarians. Age Ageing, 26, 147–151.

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