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Matti Haltia

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TOP 3
Sari Kiuru-Enari; Matti Haltia
[Hereditary gelsolin amyloidosis--40 years of Meretoja disease].
Matti Haltia
The neuronal ceroid-lipofuscinoses: from past to present.
Eija Siintola; Sanna Partanen; Petter Strömme; Aleksi Haapanen; Matti Haltia; Jan Maehlen; Anna-Elina Lehesjoki; Jaana Tyynelä
Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis.

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All Publications

2010: Sari Kiuru-Enari; Matti Haltia
[Hereditary gelsolin amyloidosis--40 years of Meretoja disease].
Duodecim; lääketieteellinen aikakauskirja 2010;126(10):1162-71.
2006: Matti Haltia
The neuronal ceroid-lipofuscinoses: from past to present.
Biochimica et biophysica acta 2006;1762(10):850-6.
2006: Eija Siintola; Sanna Partanen; Petter Strömme; Aleksi Haapanen; Matti Haltia; Jan Maehlen; Anna-Elina Lehesjoki; Jaana Tyynelä
Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis.
Brain : a journal of neurology 2006;129(Pt 6):1438-45.
2006: Tuomo Polvikoski; Raimo Sulkava; Sari Rastas; Annamaija Sutela; Leena Niinistö; Irma-Leena Notkola; Auli Verkkoniemi; Petteri Viramo; Kati Juva; Matti Haltia
Incidence of dementia in very elderly individuals: a clinical, neuropathological and molecular genetic study.
Neuroepidemiology 2006;26(2):76-82.
2005: Liisa Myllykangas; Fabienne Wavrant-De Vrièze; Tuomo Polvikoski; Irma-Leena Notkola; Raimo Sulkava; Leena Niinistö; Steven D Edland; Sampath Arepalli; Omanma Adighibe; Danielle Compton; John Hardy; Matti Haltia; Pentti J Tienari
Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: a two-stage study.
Journal of the neurological sciences 2005;236(1-2):17-24.
2005: Liisa Myllykangas; Jaana Tyynelä; Andrea Page-McCaw; Gerald M Rubin; Matti Haltia; Mel B Feany
Cathepsin D-deficient Drosophila recapitulate the key features of neuronal ceroid lipofuscinoses.
Neurobiology of disease 2005;19(1-2):194-9.
2005: Sari Kiuru-Enari; Jorma Keski-Oja; Matti Haltia
Cutis laxa in hereditary gelsolin amyloidosis.
The British journal of dermatology 2005;152(2):250-7.
2004: Jaana Tyynelä; Jonathan D Cooper; M Nadeem Khan; Stephen J A Shemilts; Matti Haltia
Hippocampal pathology in the human neuronal ceroid-lipofuscinoses: distinct patterns of storage deposition, neurodegeneration and glial activation.
Brain pathology (Zurich, Switzerland) 2004;14(4):349-57.
2004: Beathe Sitter; Taina Autti; Jaana Tyynelä; Ursula Sonnewald; Tone F Bathen; Johanna Puranen; Pirkko Santavuori; Matti Haltia; Anders Paetau; Tuomo Polvikoski; Ingrid S Gribbestad; Anna-Maija Häkkinen
High-resolution magic angle spinning and 1H magnetic resonance spectroscopy reveal significantly altered neuronal metabolite profiles in CLN1 but not in CLN3.
Journal of neuroscience research 2004;77(5):762-9.
2004: Jaana Tyynelä; Taina Autti; Matti Haltia; Sara E Mole
Pirkko Santavuori (1933-2004).
Journal of child neurology 2004;19(6):465-70.
2004: Auli Verkkoniemi; Raija Ylikoski; Juha O Rinne; Mirja Somer; Aki Hietaharju; Timo Erkinjuntti; Matti Viitanen; Hannu Kalimo; Matti Haltia
Neuropsychological functions in variant Alzheimer's disease with spastic paraparesis.
Journal of the neurological sciences 2004;218(1-2):29-37.
2003: Juha Paloneva; Jami Mandelin; Anna Kiialainen; Tom Bohling; Johannes Prudlo; Panu Hakola; Matti Haltia; Yrjo T Konttinen; Leena Peltonen
DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features.
The Journal of experimental medicine 2003;198(4):669-75.
2003: Matti Haltia
The neuronal ceroid-lipofuscinoses.
Journal of neuropathology and experimental neurology 2003;62(1):1-13.
2002: J Suopanki; Minnamaija Lintunen; Hannele Lahtinen; Matti Haltia; Pertti Panula; M Baumann; Jaana Tyynelä
Status epilepticus induces changes in the expression and localization of endogenous palmitoyl-protein thioesterase 1.
Neurobiology of disease 2002;10(3):247-57.
2002: Sari Kiuru-Enari; Hannu Somer; Anna-Maria Seppäläinen; Irma-Leena Notkola; Matti Haltia
Neuromuscular pathology in hereditary gelsolin amyloidosis.
Journal of neuropathology and experimental neurology 2002;61(6):565-71.
2002: Liisa Myllykangas; Tuomo Polvikoski; Karoliina Reunanen; Fabienne Wavrant De-Vrieze; Clare Ellis; Dena Hernandez; Raimo Sulkava; Kimmo Kontula; Auli Verkkoniemi; Irma-Leena Notkola; John Hardy; Jordi Perez-Tur; Matti Haltia; Pentti J Tienari
ApoE epsilon3-haplotype modulates Alzheimer beta-amyloid deposition in the brain.
American journal of medical genetics 2002;114(3):288-91.
2002: Sirpa Ranta; Aune Hirvasniemi; Riitta Herva; Matti Haltia; Anna-Elina Lehesjoki
[Northern epilepsy and the gene error behind it].
Duodecim; lääketieteellinen aikakauskirja 2002;118(15):1551-8.
2001: Liisa Myllykangas; Tuomo Polvikoski; Raimo Sulkava; Irma-Leena Notkola; Sari Rastas; Auli Verkkoniemi; Pentti J Tienari; Leena Niinistö; John Hardy; Jordi Pérez-Tur; Kimmo Kontula; Matti Haltia
Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study.
Annals of medicine 2001;33(7):486-92.
2001: Jukka Kallijärvi; Matti Haltia; M H Baumann
Amphoterin includes a sequence motif which is homologous to the Alzheimer's beta-amyloid peptide (Abeta), forms amyloid fibrils in vitro, and binds avidly to Abeta.
Biochemistry 2001;40(34):10032-7.
2001: Tuomo Polvikoski; Raimo Sulkava; Liisa Myllykangas; Irma-Leena Notkola; Leena Niinistö; Auli Verkkoniemi; K Kainulainen; Kimmo Kontula; Jordi Pérez-Tur; John Hardy; Matti Haltia
Prevalence of Alzheimer's disease in very elderly people: a prospective neuropathological study.
Neurology 2001;56(12):1690-6.
2001: Juha Paloneva; Taina Autti; Raili Raininko; J Partanen; O Salonen; M Puranen; Panu Hakola; Matti Haltia
CNS manifestations of Nasu-Hakola disease: a frontal dementia with bone cysts.
Neurology 2001;56(11):1552-8.
2001: Auli Verkkoniemi; Hannu Kalimo; Anders Paetau; Mirja Somer; Takeshi Iwatsubo; John Hardy; Matti Haltia
Variant Alzheimer disease with spastic paraparesis: neuropathological phenotype.
Journal of neuropathology and experimental neurology 2001;60(5):483-92.
2001: Jaana Tyynelä; Istvan Sohar; David E Sleat; RM Gin; RJ Donnelly; M Baumann; Matti Haltia; Peter Lobel
Congenital ovine neuronal ceroid lipofuscinosis--a cathepsin D deficiency with increased levels of the inactive enzyme.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2001;5 Suppl A():43-5.
2001: Matti Haltia; Riitta Herva; J Suopanki; M Baumann; Jaana Tyynelä
Hippocampal lesions in the neuronal ceroid lipofuscinoses.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2001;5 Suppl A():209-11.
2001: Sirpa Ranta; M Savukoski; Pirkko Santavuori; Matti Haltia
Studies of homogenous populations: CLN5 and CLN8.
Advances in genetics 2001;45():123-40.
2000: Henry Houlden; M Baker; E McGowan; P Lewis; Michael Hutton; Richard Crook; Nicholas W Wood; Samir Kumar-Singh; J Geddes; M Swash; Francesco Scaravilli; Janice L Holton; Tammaryn Lashley; T Tomita; T Hashimoto; Auli Verkkoniemi; Hannu Kalimo; Mirja Somer; Anders Paetau; J J Martin; Christine Van Broeckhoven; todd golde; John Hardy; Matti Haltia; Tamas Revesz
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations.
Annals of neurology 2000;48(5):806-8.
2000: Liisa Myllykangas; Tuomo Polvikoski; Raimo Sulkava; Auli Verkkoniemi; Pentti J Tienari; Leena Niinistö; Kimmo Kontula; John Hardy; Matti Haltia; Jordi Pérez-Tur
Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over.
Neuroscience letters 2000;292(3):195-8.
2000: Matti Haltia
Human prion diseases.
Annals of medicine 2000;32(7):493-500.
2000: M H Baumann; Jukka Kallijärvi; Hilkka Lankinen; C Soto; Matti Haltia
Apolipoprotein E includes a binding site which is recognized by several amyloidogenic polypeptides.
The Biochemical journal 2000;349(Pt 1):77-84.
2000: Jaana Tyynelä; Istvan Sohar; David E Sleat; RM Gin; RJ Donnelly; M Baumann; Matti Haltia; Peter Lobel
A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration.
The EMBO journal 2000;19(12):2786-92.
2000: Matt Baker; D Graff-Radford; F Wavrant-DeVrièze; Neill R Graff-Radford; Ronald C. Petersen; Emre Kokmen; Bradley Boeve; Liisa Myllykangas; Tuomo Polvikoski; Raimo Sulkava; A Verkoniemmi; Pentti J Tienari; Matti Haltia; John Hardy; Michael Hutton; Jordi Perez-Tur
No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease.
Neuroscience letters 2000;285(2):147-9.
2000: Riitta Herva; Jaana Tyynelä; Aune Hirvasniemi; M Syrjäkallio-Ylitalo; Matti Haltia
Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis.
Brain pathology (Zurich, Switzerland) 2000;10(2):215-22.
2000: Auli Verkkoniemi; Mirja Somer; Juha O Rinne; Liisa Myllykangas; Richard Crook; John Hardy; Matti Viitanen; Hannu Kalimo; Matti Haltia
Variant Alzheimer's disease with spastic paraparesis: clinical characterization.
Neurology 2000;54(5):1103-9.
2000: Mari Auranen; Juhani Rapola; Helena Pihko; Matti Haltia; Ilmo V V Leivo; Seppo Soinila; Ismo Virtanen; Hannu Kalimo; Louise V B Anderson; Pirkko Santavuori; Hannu Somer
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease.
Neuromuscular disorders : NMD 2000;10(1):16-23.
1999: Guy Prihar; A Verkkoniem; Jordi Perez-Tur; Richard Crook; Sarah J Lincoln; Henry Houlden; Mirja Somer; Anders Paetau; Hannu Kalimo; Andrew Grover; Liisa Myllykangas; Michael Hutton; John Hardy; Matti Haltia
Alzheimer disease PS-1 exon 9 deletion defined.
Nature medicine 1999;5(10):1090.
1999: Liisa Myllykangas; Tuomo Polvikoski; Raimo Sulkava; Auli Verkkoniemi; Richard Crook; Pentti J Tienari; A K Pusa; Leena Niinistö; P O'Brien; Kimmo Kontula; John Hardy; Matti Haltia; Jordi Pérez-Tur
Genetic association of alpha2-macroglobulin with Alzheimer's disease in a Finnish elderly population.
Annals of neurology 1999;46(3):382-90.
1999: A Uusitalo; K Tenhunen; Outi Kopra; Jukka O Hiltunen; M Saarma; Matti Haltia; Anu Jalanko; Leena Peltonen
Toward understanding the neuronal pathogenesis of aspartylglucosaminuria: expression of aspartylglucosaminidase in brain during development.
Molecular genetics and metabolism 1999;67(4):294-307.
1999: J Suopanki; Jaana Tyynelä; M Baumann; Matti Haltia
Palmitoyl-protein thioesterase, an enzyme implicated in neurodegeneration, is localized in neurons and is developmentally regulated in rat brain.
Neuroscience letters 1999;265(1):53-6.
1999: J Suopanki; Jaana Tyynelä; M Baumann; Matti Haltia
The expression of palmitoyl-protein thioesterase is developmentally regulated in neural tissues but not in nonneural tissues.
Molecular genetics and metabolism 1999;66(4):290-3.
1999: S Kiuru; O Salonen; Matti Haltia
Gelsolin-related spinal and cerebral amyloid angiopathy.
Annals of neurology 1999;45(3):305-11.
1999: M Baumann; P Tienari; Matti Haltia
[Views of the pathogenesis in Alzheimer's disease are changing].
Duodecim; lääketieteellinen aikakauskirja 1999;115(7):767-76.
1998: K Tenhunen; A Uusitalo; Taina Autti; Raimo Joensuu; M Kettunen; Risto A Kauppinen; S Ikonen; Mary E LaMarca; Matti Haltia; Edward I Ginns; Anu Jalanko; Leena Peltonen
Monitoring the CNS pathology in aspartylglucosaminuria mice.
Journal of neuropathology and experimental neurology 1998;57(12):1154-63.
1998: Richard Crook; Auli Verkkoniemi; Jordi Perez-Tur; N Mehta; Matt Baker; Henry Houlden; Matthew J Farrer; Michael Hutton; Sarah J Lincoln; John Hardy; Katrina Gwinn-Hardy; Mirja Somer; Anders Paetau; Hannu Kalimo; Raija Ylikoski; M Pöyhönen; S Kucera; Matti Haltia
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1.
Nature medicine 1998;4(4):452-5.
1998: Auli Verkkoniemi; Mirja Somer; Matti Haltia
[New variant of Alzheimer's disease].
Duodecim; lääketieteellinen aikakauskirja 1998;114(24):2509-11.
1998: M Oinas; Tuomo Polvikoski; Raimo Sulkava; Anders Paetau; Matti Haltia
[Lewy body dementia].
Duodecim; lääketieteellinen aikakauskirja 1998;114(15):1476-83.
1998: Pirkko Santavuori; Leena Valanne; Taina Autti; Matti Haltia; Helena Pihko; Kirsi Sainio
Muscle-eye-brain disease: clinical features, visual evoked potentials and brain imaging in 20 patients.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1998;2(1):41-7.
1997: Taina Autti; Raili Raininko; Matti Haltia; Leena Lauronen; Sanna-Leena Vanhanen; O Salonen; Hannu J Aronen; Kari O Wirtavuori; Pirkko Santavuori
Aspartylglucosaminuria: radiologic course of the disease with histopathologic correlation.
Journal of child neurology 1997;12(6):369-75.
1997: Taina Autti; Raili Raininko; Pirkko Santavuori; Sanna-Leena Vanhanen; Veli-Pekka Poutanen; Matti Haltia
MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type.
Neuroradiology 1997;39(5):371-7.
1997: Anu Suomalainen; A Majander; M Wallin; Kirsi Setälä; Kimmo Kontula; H Leinonen; T Salmi; Anders Paetau; Matti Haltia; Leena Valanne; J Lonnqvist; Leena Peltonen; Hannu Somer
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.
Neurology 1997;48(5):1244-53.
1997: Jaana Tyynelä; J Suopanki; Pirkko Santavuori; M Baumann; Matti Haltia
Variant late infantile neuronal ceroid-lipofuscinosis: pathology and biochemistry.
Journal of neuropathology and experimental neurology 1997;56(4):369-75.
1997: Jaana Tyynelä; J Suopanki; M Baumann; Matti Haltia
Sphingolipid activator proteins (SAPs) in neuronal ceroid lipofuscinoses (NCL).
Neuropediatrics 1997;28(1):49-52.
1997: Matti Haltia; Ilmo V V Leivo; Hannu Somer; Helena Pihko; Anders Paetau; T Kivelä; Ahti Tarkkanen; F Tomé; E Engvall; Pirkko Santavuori
Muscle-eye-brain disease: a neuropathological study.
Annals of neurology 1997;41(2):173-80.
1996: E Hatva; Juha Jääskeläinen; H Hirvonen; Kari Alitalo; Matti Haltia
Tie endothelial cell-specific receptor tyrosine kinase is upregulated in the vasculature of arteriovenous malformations.
Journal of neuropathology and experimental neurology 1996;55(11):1124-33.
1996: Tom Böhling; A Mäenpää; Tuomo Timonen; L Vantunen; A Paetau; Matti Haltia
Different expression of adhesion molecules on stromal cells and endothelial cells of capillary hemangioblastoma.
Acta neuropathologica 1996;92(5):461-6.
1996: D M A Mann; Takeshi Iwatsubo; Nigel J Cairns; P L Lantos; David Nochlin; Shuzo M Sumi; Thomas D Bird; Parvoneh Poorkaj-Navas; John Hardy; Michael Hutton; Guy Prihar; Richard Crook; Martin N Rossor; Matti Haltia
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43).
Annals of neurology 1996;40(2):149-56.
1996: R Sulkava; K Kainulainen; Auli Verkkoniemi; Leena Niinistö; E Sobel; Z Davanipour; Tuomo Polvikoski; Matti Haltia; K Kontula
APOE alleles in Alzheimer's disease and vascular dementia in a population aged 85+.
Neurobiology of aging 1996;17(3):373-6.
1996: Tom Böhling; E Hatva; M Kujala; L Claesson-Welsh; Kari Alitalo; Matti Haltia
Expression of growth factors and growth factor receptors in capillary hemangioblastoma.
Journal of neuropathology and experimental neurology 1996;55(5):522-7.
1996: E Hatva; Tom Böhling; Juha Jääskeläinen; M G Persico; Matti Haltia; Kari Alitalo
Vascular growth factors and receptors in capillary hemangioblastomas and hemangiopericytomas.
The American journal of pathology 1996;148(3):763-75.
1996: Tom Böhling; O Turunen; Juha Jääskeläinen; O Carpen; Markku Sainio; T Wahlström; Antti Vaheri; Matti Haltia
Ezrin expression in stromal cells of capillary hemangioblastoma. An immunohistochemical survey of brain tumors.
The American journal of pathology 1996;148(2):367-73.
1996: Matti Haltia; A von Hertzen
[Nurses and doctors uniforms in Finland during the years 1600-1900].
Duodecim; lääketieteellinen aikakauskirja 1996;112(23):2283-300.
1996: R Sulkava; K Kontula; Matti Haltia
[Recent genetic association in Alzheimer's disease].
Duodecim; lääketieteellinen aikakauskirja 1996;112(8):651, 653, 655.
1995: Tuomo Polvikoski; R Sulkava; Matti Haltia; K Kainulainen; Alpo F Vuorio; Auli Verkkoniemi; Leena Niinistö; P Halonen; Kimmo Kontula
Apolipoprotein E, dementia, and cortical deposition of beta-amyloid protein.
The New England journal of medicine 1995;333(19):1242-7.
1995: Sanna-Leena Vanhanen; Raili Raininko; Pirkko Santavuori; Taina Autti; Matti Haltia
MRI evaluation of the brain in infantile neuronal ceroid-lipofuscinosis. Part 1: Postmortem MRI with histopathologic correlation.
Journal of child neurology 1995;10(6):438-43.
1995: M T Seppälä; Matti Haltia; Risto Sankila; Juha Jääskeläinen; O Heiskanen
Long-term outcome after removal of spinal schwannoma: a clinicopathological study of 187 cases.
Journal of neurosurgery 1995;83(4):621-6.
1995: Annamari Ranki; M Nyberg; Vladimir Ovod; Matti Haltia; Irina Elovaara; Raili Raininko; H Haapasalo; Kai Krohn
Abundant expression of HIV Nef and Rev proteins in brain astrocytes in vivo is associated with dementia.
AIDS (London, England) 1995;9(9):1001-8.
1995: Jaana Tyynelä; M Baumann; M Henseler; K Sandhoff; Matti Haltia
Sphingolipid activator proteins (SAPs) are stored together with glycosphingolipids in the infantile neuronal ceroid-lipofuscinosis (INCL).
American journal of medical genetics 1995;57(2):294-7.
1995: M T Seppälä; Matti Haltia; Risto Sankila; Juha Jääskeläinen; O Heiskanen
Long-term outcome after removal of spinal neurofibroma.
Journal of neurosurgery 1995;82(4):572-7.
1995: E Hatva; A Kaipainen; P Mentula; Juha Jääskeläinen; A Paetau; Matti Haltia; Kari Alitalo
Expression of endothelial cell-specific receptor tyrosine kinases and growth factors in human brain tumors.
The American journal of pathology 1995;146(2):368-78.
1995: Matti Haltia; Jaana Tyynelä; M Baumann; M Henseler; K Sandhoff
Immunological studies on sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses.
Gerontology 1995;41 Suppl 2():239-48.
1995: Jaana Tyynelä; M Baumann; M Henseler; K Sandhoff; Matti Haltia
Sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses: an immunological study.
Acta neuropathologica 1995;89(5):391-8.
1994: S Kiuru; E Matikainen; M Kupari; Matti Haltia; Jukka U Palo
Autonomic nervous system and cardiac involvement in familial amyloidosis, Finnish type (FAF).
Journal of the neurological sciences 1994;126(1):40-8.
1994: Tero Kivelä; Ahti Tarkkanen; Blas Frangione; Jorge Ghiso; Matti Haltia
Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndrome.
Investigative ophthalmology & visual science 1994;35(10):3759-69.
1994: Matti Haltia; Matti Viitanen; R Sulkava; V Ala-Hurula; M Poyhonen; Lev G Goldfarb; P Brown; Efrat Levy; Henry Houlden; Richard Crook
Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description.
Annals of neurology 1994;36(3):362-7.
1993: Tero Kivelä; Ahti Tarkkanen; I McLean; Jorge Ghiso; Blas Frangione; Matti Haltia
Immunohistochemical analysis of lattice corneal dystrophies types I and II.
The British journal of ophthalmology 1993;77(12):799-804.
1993: M T Seppälä; Matti Haltia
Spinal malignant nerve-sheath tumor or cellular schwannoma? A striking difference in prognosis.
Journal of neurosurgery 1993;79(4):528-32.
1993: Jaana Tyynelä; David N Palmer; M Baumann; Matti Haltia
Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis.
FEBS letters 1993;330(1):8-12.
1993: Lev G Goldfarb; Paul Brown; Matti Haltia; Jorge Ghiso; Blas Frangione; D Carleton Gajdusek
Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrils.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(10):4451-4.
1993: Matti Haltia; Mirja Somer
Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome).
Acta neuropathologica 1993;85(3):241-7.
1992: Matti Haltia; Anu Suomalainen; A Majander; Hannu Somer
Disorders associated with multiple deletions of mitochondrial DNA.
Brain pathology (Zurich, Switzerland) 1992;2(2):133-9.
1992: Paul Brown; Lev G Goldfarb; J Kovanen; Matti Haltia; F Cathala; M Sulima; CJ Gibbs; D Carleton Gajdusek
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation.
Annals of neurology 1992;31(3):282-5.
1992: Lev G Goldfarb; Paul Brown; Matti Haltia; F Cathala; W R McCombie; J Kovanen; L Cervenáková; L Goldin; A Nieto; M S Godec
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin.
Annals of neurology 1992;31(3):274-81.
1992: Matti Haltia; Efrat Levy; J Meretoja; I Fernandez-Madrid; O Koivunen; Blas Frangione
Gelsolin gene mutation--at codon 187--in familial amyloidosis, Finnish: DNA-diagnostic assay.
American journal of medical genetics 1992;42(3):357-9.
1992: Helena Pihko; Anu Suomalainen; Hannu Somer; Matti Haltia; A Majander
[Mitochondrial diseases].
Duodecim; lääketieteellinen aikakauskirja 1992;108(6):578-90.
1991: Matti Haltia; J Kovanen; Lev G Goldfarb; P Brown; D Carleton Gajdusek
Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies.
European journal of epidemiology 1991;7(5):494-500.
1991: Matti Haltia; Jorge Ghiso; Thomas Wisniewski; S Kiuru; D Miller; Blas Frangione
Gelsolin variant and beta-amyloid co-occur in a case of Alzheimer's with Lewy bodies.
Neurobiology of aging 1991;12(4):313-6.
1991: Thomas Wisniewski; Matti Haltia; Jorge Ghiso; Blas Frangione
Lewy bodies are immunoreactive with antibodies raised to gelsolin related amyloid-Finnish type.
The American journal of pathology 1991;138(5):1077-83.
1991: R Salonen; Mirja Somer; Matti Haltia; M Lorentz; Reijo Norio
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome).
Clinical genetics 1991;39(4):287-93.
1991: E Poutiainen; Matti Haltia; Irina Elovaara; J Lähdevirta; M Iivanainen
Dementia associated with human immunodeficiency virus: subcortical or cortical?
Acta psychiatrica Scandinavica 1991;83(4):297-301.
1991: Lev G Goldfarb; Matti Haltia; P Brown; A Nieto; J Kovanen; W R McCombie; S Trapp; D Carleton Gajdusek
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred.
Lancet 1991;337(8738):425.
1990: Jorge Ghiso; Matti Haltia; F Prelli; J Novello; Blas Frangione
Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
The Biochemical journal 1990;272(3):827-30.
1990: Efrat Levy; Matti Haltia; I Fernandez-Madrid; O Koivunen; Jorge Ghiso; F Prelli; Blas Frangione
Mutation in gelsolin gene in Finnish hereditary amyloidosis.
The Journal of experimental medicine 1990;172(6):1865-7.
1990: Matti Haltia; Jorge Ghiso; F Prelli; Gloria Gallo; S Kiuru; Hannu Somer; Jukka U Palo; Blas Frangione
Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin.
The American journal of pathology 1990;136(6):1223-8.
1990: Matti Haltia; F Prelli; Jorge Ghiso; S Kiuru; Hannu Somer; Jukka U Palo; Blas Frangione
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein.
Biochemical and biophysical research communications 1990;167(3):927-32.
1990: Antti Servo; M Porras; Juha Jääskeläinen; A Paetau; Matti Haltia
Computed tomography and angiography do not reliably discriminate malignant meningiomas from benign ones.
Neuroradiology 1990;32(2):94-7.
1988: Risto Roine; M Hillbom; M Valle; Matti Haltia; L Ketonen; E Neuvonen; J Lumio; J Lähdevirta
Fatal encephalitis caused by a bat-borne rabies-related virus. Clinical findings.
Brain : a journal of neurology 1988;111 ( Pt 6)():1505-16.
1988: Hannu Heiskala; Hannu Somer; J Kovanen; E Poutiainen; H Karli; Matti Haltia
Microangiopathy with encephalopathy, hearing loss and retinal arteriolar occlusions: two new cases.
Journal of the neurological sciences 1988;86(2-3):239-50.
1988: Timo Erkinjuntti; Matti Haltia; Jukka U Palo; Raimo Sulkava; A Paetau
Accuracy of the clinical diagnosis of vascular dementia: a prospective clinical and post-mortem neuropathological study.
Journal of neurology, neurosurgery, and psychiatry 1988;51(8):1037-44.
1988: Matti Haltia; Hannu Somer; S Rehunen
Congenital fiber type disproportion in an adult: a morphometric and microchemical study.
Acta neurologica Scandinavica 1988;78(1):65-71.
1988: J Kovanen; Matti Haltia
Descriptive epidemiology of Creutzfeldt-Jakob disease in Finland.
Acta neurologica Scandinavica 1988;77(6):474-80.
1987: Tom Böhling; Matti Haltia; K Rosenlöf; Frej Fyhrquist
Erythropoietin in capillary hemangioblastoma. An immunohistochemical study.
Acta neuropathologica 1987;74(4):324-8.
1986: J Lumio; M Hillbom; R Roine; L Ketonen; Matti Haltia; M Valle; E Neuvonen; J Lähdevirta
Human rabies of bat origin in Europe.
Lancet 1986;1(8477):378.
1985: J Kovanen; Timo Erkinjuntti; M Iivanainen; L Ketonen; Matti Haltia; R Sulkava; Jorma Sipponen
Cerebral MR and CT imaging in Creutzfeldt-Jakob disease.
Journal of computer assisted tomography 1985;9(1):125-8.
1985: K Rosenlöf; Frej Fyhrquist; C Grönhagen-Riska; Tom Böhling; Matti Haltia
Erythropoietin and renin substrate in cerebellar haemangioblastoma.
Acta medica Scandinavica 1985;218(5):481-5.
1983: Tom Böhling; A Paetau; P Ekblom; Matti Haltia
Distribution of endothelial and basement membrane markers in angiogenic tumors of the nervous system.
Acta neuropathologica 1983;62(1-2):67-72.