9 results for author:"Ibanez P." in Literature citations
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| Overexpression of p73 as a tissue marker for high-risk gastritis. Carrasco G., Diaz J., Valbuena J.R., Ibanez P., Rodriguez P., Araya G., Rodriguez C., Torres J., Duarte I., Aravena E. et al. Clin. Cancer Res. 16:3253-3259(2010) · Mapped (4) |
| Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms. Ibanez P., Lesage S., Janin S., Lohmann E., Durif F., Destee A., Bonnet A.M., Brefel-Courbon C., Heath S., Zelenika D. et al. Arch. Neurol. 66:102-108(2009) · Mapped (7) |
| Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1. Leutenegger A.-L., Salih M.A.M., Ibanez P., Mukhtar M.M., Lesage S., Arabi A., Lohmann E., Duerr A., Ahmed A.E.M., Brice A. Arch. Neurol. 63:1257-1261(2006) · UniProtKB (1) |
| Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. The French Parkinson's disease genetics study group Brain 129:686-694(2006) · UniProtKB (1) |
| G2019S LRRK2 mutation in French and North African families with Parkinson's disease. French Parkinson's disease genetics study group |
| LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. Lesage S., Leutenegger A.L., Ibanez P., Janin S., Lohmann E., Durr A., Brice A. Am. J. Hum. Genet. 77:330-332(2005) · Mapped (4) |
| Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism. Ibanez P., De Michele G., Bonifati V., Lohmann E., Thobois S., Pollak P., Agid Y., Heutink P., Durr A., Brice A. Neurology 61:1429-1431(2003) · Mapped (1) |
| Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse. Itier J.M., Ibanez P., Mena M.A., Abbas N., Cohen-Salmon C., Bohme G.A., Laville M., Pratt J., Corti O., Pradier L. et al. Hum. Mol. Genet. 12:2277-2291(2003) · Mapped (9) |
| Mutations in the DJ-1 gene associated with autosomal recessive early-onset Parkinsonism. Bonifati V., Rizzu P., van Baren M.J., Schaap O., Breedveld G.J., Krieger E., Dekker M.C.J., Squitieri F., Ibanez P., Joosse M. et al. |