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T313M PINK1 mutation in an extended highly consanguineous Saudi family with
early-onset Parkinson disease.
Chishti MA, Bohlega S, Ahmed M, Loualich A, Carroll P, Sato C, St George-Hyslop P, Westaway D, Rogaeva E.
A clinic and a paraclinic study of Tunisian population of children with autism.
About 63 cases]
Belhadj A, Mrad R, Halayem MB.
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American
Caucasian Parkinson's disease families.
Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango et. al
Depression and generalised anxiety in the general population in Belgium: a
comparison between native and immigrant groups.
Levecque K, Lodewyckx I, Vranken J.