Items where Author is "Medeiros, Helena"

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Article

Balance of care (deinstitutionalisation in Europe): results from the Mental Health Economics European Network (MHEEN). Knapp, Martin; McDaid, David; Medeiros, Helena

Benign hereditary chorea: clinical, genetic, and pathological findings. Kleiner-Fishman, Galit; Rogaeva, Ekaterina; Halliday, William; Houle, Sylvain; Kawarai, Toshitaka; Sato, Christine; Medeiros, Helena; St. George-Hyslop, Peter H.; Lang, Anthony E.

Clinical findings in a large family with a parkin ex3delta40 mutation. Munhoz, Renato P.; Sa, Daniel S.; Rogaeva, Ekaterina; Salehi-Rad, Shabnam; Sato, Christine; Medeiros, Helena; Farrer, Matthew; Lang, Anthony E.

Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease. Nicolaou, M.; Song, Y-Q.; Sato, C. A.; Orlacchio, A.; Kawarai, T.; Medeiros, Helena; Liang, Y.; Sorbi, S.; Richard, E.; Rogaev, E. I.; Moliaka, Y; Bruni, A. C.; Jorge, R.; Percy, M.; Duara, R.; Farrer, L. A.; St George-Hyslop, P.; Rogaeva, E. A.

Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease. Devi, Gayatria; Fotiou, Alexandra; Jyrinji, Darlene; Tycko, Benjamin; DeArmand, Steve; Rogaeva, Ekaterina; Song, You-Quiang; Medeiros, Helena; Liang, Yan; Orlacchio, Antonio; Williamson, Jennifer; St George-Hyslop, Peter; Mayeux, Richard

Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations. Rogaeva, E. A.; Fafel, K. C.; Song, Y. Q.; Medeiros, Helena; Sato, C.; Liang, Y.; Richard, E.; Rogaev, E. I.; Frommelt, P.; Sadovnick, A. D.; Meschino, W.; Rockwood, K.; Boss, M. A.; Mayeux, R.; St. George–Hyslop, P.