Characterization of a cyclooxygenase-2-765G→C promoter polymorphism in human neural cellsCUI, Jian-Guo; SALEHI-RAD, Shabnam; ROGAEVA, Ekaterina et al.Neuroreport (Oxford). 2005, Vol 16, Num 6, pp 575-579, issn 0959-4965, 5 p.Article

Clinical findings in a large family with a parkin Ex3Δ40 mutationMUNHOZ, Renato P; SA, Daniel S; ROGAEVA, Ekaterina et al.Archives of neurology (Chicago). 2004, Vol 61, Num 5, pp 701-704, issn 0003-9942, 4 p.Article

Novel SPG6 mutation p.A100T in a japanese family with autosomal dominant form of hereditary spastic paraplegiaKANEKO, Satoshi; KAWARAI, Toshitaka; ST GEORGE-HYSLOP, Peter et al.Movement disorders. 2006, Vol 21, Num 9, pp 1531-1533, issn 0885-3185, 3 p.Article

Analysis of the glucocerebrosidase gene in Parkinson's diseaseSATO, Christine; MORGAN, Angharad; LANG, Anthony E et al.Movement disorders. 2004, Vol 20, Num 3, pp 367-370, issn 0885-3185, 4 p.Article

Childhood onset in familial prion disease with a novel mutation in the PRNP geneROGAEVA, Ekaterina; ZADIKOFF, Cindy; PONESSE, Jonathan et al.Archives of neurology (Chicago). 2006, Vol 63, Num 7, pp 1016-1021, issn 0003-9942, 6 p.Article