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Matti Haltia

Medical University of Vienna

70H指数
332论文数
1.6W被引数
收录论文 40
发表时间
Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)致编辑的信: 神经元核内包涵体疾病中的Hornerin沉积: Park等人直接鉴定包涵体中具有成分偏倚区域的蛋白质 (2022)
err2024-01-02
err0
errOAAI
errLuo, Huihui; Gustavsson, Emil K.; Macpherson, Hannah; Dominik, Natalia; Zhelcheska, Kristina; Montgomery, Kylie; Anderson, Claire; Yau, Wai Yan; Efthymiou, Stephanie; Turner, Chris; DeTure, Michael; Dickson, Dennis W.; Josephs, Keith A.; Revesz, Tamas; Lashley, Tammaryn; Halliday, Glenda; Rowe, Dominic B.; McCann, Emily; Blair, Ian; Lees, Andrew J.; Tienari, Pentti J.; Suomalainen, Anu; Molina-Porcel, Laura; Kovacs, Gabor G.; Gelpi, Ellen; Hardy, John; Haltia, Matti J.; Tucci, Arianna; Jaunmuktane, Zane; Ryten, Mina; Houlden, Henry; Chen, Zhongbo
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Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions
err2022-03-04
err7
errOAAI
errPark, Hongsun; Yamanaka, Tomoyuki; Toyama, Yumiko; Fujita, Atsushi; Doi, Hiroshi; Nirasawa, Takashi; Murayama, Shigeo; Matsumoto, Naomichi; Shimogori, Tomomi; Ikegawa, Masaya; Haltia, Matti J.; Nukina, Nobuyuki
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Neuronal intranuclear inclusion disease is genetically heterogeneous
err2020-08-10
err49
errOAAI
errChen, Zhongbo; Yau, Wai Yan; Jaunmuktane, Zane; Tucci, Arianna; Sivakumar, Prasanth; Taliun, Sarah A. Gagliano; Turner, Chris; Efthymiou, Stephanie; Ibanez, Kristina; Sullivan, Roisin; Bibi, Farah; Athanasiou-Fragkouli, Alkyoni; Bourinaris, Thomas; Zhang, David; Revesz, Tamas; Lashley, Tammaryn; DeTure, Michael; Dickson, Dennis W.; Josephs, Keith A.; Gelpi, Ellen; Kovacs, Gabor G.; Halliday, Glenda; Rowe, Dominic B.; Blair, Ian; Tienari, Pentti J.; Suomalainen, Anu; Fox, Nick C.; Wood, Nicholas W.; Lees, Andrew J.; Haltia, Matti J.; Hardy, John; Ryten, Mina; Vandrovcova, Jana; Houlden, Henry
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Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction:: a population-based neuropathological study
err2009-07-08
err36
PREAI
errMyllykangas, L; Polvikoski, T; Sulkava, R; Notkola, IL; Rastas, S; Verkkoniemi, A; Tienari, PJ; Niinistö, L; Hardy, J; Pérez-Tur, J; Kontula, K; Haltia, M
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Neuronal ceroid-lipofuscinosis - Late-infantile or Jansky-Bielschowsky type - Revisited
err2008-01-28
err18
PREAI
errGoebel, HH; Gerhard, L; Kominami, E; Haltia, M
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Chromosome 21 BACE2 haplotype associates with Alzheimer's disease:: A two-stage study
err2005-09-01
err29
PREAI
errMyllykangas, L; Wavrant-De Vrièze, F; Polvikoski, T; Notkola, IL; Sulkava, R; Niinistö, L; Edland, SD; Arepalli, S; Adighibe, O; Compton, D; Hardy, J; Haltia, M; Tienari, PJ
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Cutis laxa in hereditary gelsolin amyloidosis
err2005-02-01
err46
PREAI
errKiuru-Enari, S; Keski-Oja, J; Haltia, M
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Multiple sclerosis: In situ evidence for antibody and complement-mediated demyelination
err2004-10-08
err368
PREAI
errStorch, MK; Piddlesden, S; Haltia, M; Iivanainen, M; Morgan, P; Lassmann, H
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Amyloid beta protein (A beta) deposition in chromosome 14-linked Alzheimer's disease: Predominance of A beta(42(43))
err2004-10-08
err203
PREAI
errMann, DMA; Iwatsubo, T; Cairns, NJ; Lantos, PL; Nochlin, D; Sumi, SM; Bird, TD; Poorkaj, P; Hardy, J; Hutton, M; Prihar, G; Crook, R; Rossor, MN; Haltia, M
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Muscle-eye-brain disease: A neuropathological study
err2004-10-08
err126
PREAI
errHaltia, M; Leivo, I; Somer, H; Pihko, H; Paetau, A; Kivela, T; Tarkkanen, A; Tome, F; Engvall, E; Santavuori, P
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Neuropsychological functions in variant Alzheimer's disease with spastic paraparesis
err2004-03-01
err5
PREAI
errVerkkoniemi, A; Ylikoski, R; Rinne, JO; Somer, M; Hietaharju, A; Erkinjuntti, T; Viitanen, M; Kalimo, H; Haltia, M
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Contribution of APOE promoter polymorphisms to Alzheimer's disease risk
err2002-07-09
err109
PREAI
errLambert, JC; Araria-Goumidi, L; Myllykangas, L; Ellis, C; Wang, JC; Bullido, MJ; Harris, JM; Artiga, MJ; Hernandez, D; Kwon, JM; Frigard, B; Petersen, RC; Cumming, AM; Pasquier, F; Sastre, I; Tienari, PJ; Frank, A; Sulkava, R; Morris, JC; St Clair, D; Mann, DM; Wavrant-DeVrièze, F; Ezquerra-Trabalon, M; Amouyel, P; Hardy, J; Haltia, M; Valdivieso, F; Goate, AM; Pérez-Tur, J; Lendon, CL; Chartier-Harlin, MC
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Neuromuscular pathology in hereditary gelsolin amyloidosis
err2002-06-01
err54
errOAAI
errKiuru-Enari, S; Somer, H; Seppäläinen, AM; Notkola, IL; Haltia, M
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Prevalence of Alzheimer's disease in very elderly people -: A prospective neuropathological study
err2001-06-26
err136
PREAI
errPolvikoski, T; Sulkava, R; Myllykangas, L; Notkola, IL; Niinistö, L; Verkkoniemi, A; Kainulainen, K; Kontula, K; Pérez-Tur, J; Hardy, J; Haltia, M
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CNS manifestations of Nasu-Hakola disease - A frontal dementia with bone cysts
err2001-06-12
err179
PREAI
errPaloneva, J; Autti, T; Raininko, R; Partanen, J; Salonen, O; Puranen, M; Hakola, P; Haltia, M
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Variant Alzheimer disease with spastic paraparesis: Neuropathological phenotype
err2001-05-01
err86
errOAAI
errVerkkoniemi, A; Kalimo, H; Paetau, A; Somer, M; Iwatsubo, T; Hardy, J; Haltia, M
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Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-β concentrations
err2000-11-01
err125
PREAI
errHoulden, H; Baker, M; McGowan, E; Lewis, P; Hutton, M; Crook, R; Wood, NW; Kumar-Singh, S; Geddes, J; Swash, M; Scaravilli, F; Holton, JL; Lashley, T; Tomita, T; Hashimoto, T; Verkkoniemi, A; Kalimo, H; Somer, M; Paetau, A; Martin, JJ; Van Broeckhoven, C; Golde, T; Hardy, J; Haltia, M; Revesz, T
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Apolipoprotein E includes a binding site which is recognized by several amyloidogenic polypeptides
err2000-07-01
err35
errOAAI
errBaumann, MH; Kallijärvi, J; Lankinen, H; Soto, C; Haltia, M
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