Mattu Haltia- Selected publications#

  • Goldfarb LG, Haltia M, Brown P, Nieto A, Kovanen J, McCombie WR, Trapp S, Gajdusek DC: New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred. Lancet 1991; 337: 425.
  • Haltia M, Viitanen M, Sulkava R, Ala-Hurula V, Pöyhönen M, Goldfarb L, Brown P, Levy E, Houlden H, Crook R, Goate A, Clark R, Korenblat K, Pandit S, Keller HD, Lilius L, Liu L, Axelman K, Forsell, L, Winblad B, Lannfelt L, Hardy J: Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description. Ann Neurol 1994, 36: 362–367.
  • Alzheimer's Disease Collaborative Group (including M. Haltia): The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. Nature Genet 1995, 11: 219–222.
  • Polvikoski T, Sulkava R, Haltia M, Kainulainen K, Vuorio A, Verkkoniemi A, Niinisto L, Halonen P, Kontula K: Apolipoprotein E, dementia, and cortical deposition of beta-amyloid protein. New Engl J Med 1995, 333: 1242–1247.
  • Crook R, Verkkoniemi A, Perez-Tur J, Mehta N, Baker M, Houlden H, Farrer M, Hutton M, Lincoln S, Hardy J, Gwinn K, Somer M, Paetau A, Kalimo H, Ylikoski R, Poyhonen M, Kucera S, Haltia M: A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. Nature Med 1998, 4: 452–455.
  • Kiuru S, Salonen O, Haltia M: Gelsolin- related spinal and cerebral amyloid angiopathy. Ann Neurol 1999, 45: 305–311.
  • Prihar G, Verkkoniemi A, Perez-Tur J, Crook R, Lincoln S, Houlden H, Somer M, Paetau A, Kalimo H, Grover A, Myllykangas L, Hutton M, Hardy J, Haltia M: Alzheimer disease PS-1 exon 9 deletion defined. Nature Med 1999, 5: 1090–1090.
  • Herva R, Tyynelä J, Hirvasniemi A, Syrjäkallio-Ylitalo M, Haltia M.: Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis. Brain Pathol 2000, 10: 215–222.
  • Verkkoniemi A, Somer M, Rinne JO, Myllykanga L, Crook R, Hardy J, Viitanen M, Kalimo H, Haltia M: Variant Alzheimer´s disease with spastic paraparesis. Clinical characterization. Neurology 2000, 54: 1103–1109.
  • Verkkoniemi A, Kalimo H, Paetau A, Somer M, Iwatsubo T, Hardy J, Haltia M: Variant Alzheimer disease with spastic paraparesis: Neuropathological phenotype. J Neuropathol Exp Neurol 2001, 60: 483–492.


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