Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain von Yamamoto, Y., Craggs, L., Baumann, M., Kalimo, H., Kalaria, R. N.

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PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease von Koivunen, J., Verkkoniemi, A., Aalto, S., Paetau, A., Ahonen, J.-P., Viitanen, M., Någren, K., Rokka, J., Haaparanta, M., Kalimo, H., Rinne, J. O.

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Prevalence and severity of cerebral amyloid angiopathy: a population-based study on very elderly Finns (Vantaa 85+) von Tanskanen, M., Mäkelä, M., Myllykangas, L., Notkola, I.-L., Polvikoski, T., Sulkava, R., Kalimo, H., Paetau, A.

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Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases von Craggs, Lucinda, Taylor, Julie, Slade, Janet Y., Chen, Aiqing, Hagel, Christian, Kuhlenbaeumer, Gregor, Borjesson-Hanson, Anne, Viitanen, Matti, Kalimo, Hannu, Deramecourt, Vincent, Oakley, Arthur E., Kalaria, Raj N.

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Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease von MAURAGE, C. A, UDD, B, RUCHOUX, M. M, VERMERSCH, P, KALIMO, H, KRAHE, R, DELACOURTE, A, SERGEANT, N

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MR Imaging Characteristics and Neuropathology of the Spinal Cord in Adult-Onset Autosomal Dominant Leukodystrophy with Autonomic Symptoms von Sundblom, J, Melberg, A, Kalimo, H, Smits, A, Raininko, R

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MR Characteristics and Neuropathology in Adult-Onset Autosomal Dominant Leukodystrophy with Autonomic Symptoms von Melberg, A, Hallberg, L, Kalimo, H, Raininko, R

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Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL von Low, W. C., Junna, M., Börjesson-Hanson, A., Morris, C. M., Moss, T. H., Stevens, D. L., St Clair, D., Mizuno, T., Zhang, W. W., Mykkänen, K., Wahlstrom, J., Andersen, O., Kalimo, H., Viitanen, M., Kalaria, R. N.

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Relation between myofibers and connective tissue during muscle injury repair von Kääriäinen, M., Järvinen, T., Järvinen, M., Rantanen, J., Kalimo, H.

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Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes von Rostedt Punga, A., Ahlqvist, K., Bartoccioni, E., Scuderi, F., Marino, M., Suomalainen, A., Kalimo, H., Stålberg, E.V.

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Increased brain histamine levels in Parkinson's disease but not in multiple system atrophy von Rinne, J. O., Anichtchik, O. V., Eriksson, K. S., Kaslin, J., Tuomisto, L., Kalimo, H., Röyttä, M., Panula, P.

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The pathogenesis of CADASIL: an update von Kalaria, R.N., Viitanen, M., Kalimo, H., Dichgans, M., Tabira, T.

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CADASIL and CARASIL von Tikka, Saara, Baumann, Marc, Siitonen, Maija, Pasanen, Petra, Pöyhönen, Minna, Myllykangas, Liisa, Viitanen, Matti, Fukutake, Toshio, Cognat, Emmanuel, Joutel, Anne, Kalimo, Hannu

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The tau S305S mutation causes frontotemporal dementia with parkinsonism von Skoglund, L., Viitanen, M., Kalimo, H., Lannfelt, L., Jönhagen, M. E., Ingelsson, M., Glaser, A., Herva, R.

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Stable expression of mutated and non-mutated mouse NOTCH3 in C2C12 mouse myoblast von Ng, Y.P, Kalimo, H, Baumann, M

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Neuronal histamine deficit in Alzheimer's disease von Panula, P, Rinne, J, Kuokkanen, K, Eriksson, K.S, Sallmen, T, Kalimo, H, Relja, M

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G.P.7.03 Mutations in TPM2 and TPM3 causing nemaline myopathy or arthrogryposis von Lehtokari, V.L, Kalimo, H, Pelin, K, Wallgren-Pettersson, C

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Reappraisal of a consecutive autopsy series of patients with primary degenerative dementia: Lewy-related pathology von OINAS, M., SULKAVA, R., POLVIKOSKI, T., KALIMO, H., PAETAU, A.

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Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients von Tikka, Saara, Mykkänen, Kati, Ruchoux, Marie-Magdeleine, Bergholm, Robert, Junna, Maija, Pöyhönen, Minna, Yki-Järvinen, Hannele, Joutel, Anne, Viitanen, Matti, Baumann, Marc, Kalimo, Hannu

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Neurologic symptoms are common during gestation and puerperium in CADASIL von ROINE, S, PÖYHÖNEN, M, TIMONEN, S, TUISKU, S, MARTTILA, R, SULKAVA, R, KALIMO, H, VIITANEN, M

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