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Items: 1 to 50 of 331

1.

Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1.

Siitonen M, Börjesson-Hanson A, Pöyhönen M, Ora A, Pasanen P, Bras J, Kern S, Kern J, Andersen O, Stanescu H, Kleta R, Baumann M, Kalaria R, Kalimo H, Singleton A, Hardy J, Viitanen M, Myllykangas L, Guerreiro R.

Brain. 2017 May 1;140(5):e29. doi: 10.1093/brain/awx062. No abstract available.

2.

Cardiac autophagic vacuolation in severe X-linked myopathy with excessive autophagy.

Munteanu I, Kalimo H, Saraste A, Nishino I, Minassian BA.

Neuromuscul Disord. 2017 Feb;27(2):185-187. doi: 10.1016/j.nmd.2016.10.007. Epub 2016 Oct 19.

PMID:
27916343
3.

Gelsolin amyloid angiopathy causes severe disruption of the arterial wall.

Koskelainen S, Pihlamaa T, Suominen S, Zhao F, Salo T, Risteli J, Baumann M, Kalimo H, Kiuru-Enari S.

APMIS. 2016 Aug;124(8):639-48. doi: 10.1111/apm.12554. Epub 2016 May 20.

PMID:
27198069
4.

Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases.

Craggs L, Taylor J, Slade JY, Chen A, Hagel C, Kuhlenbaeumer G, Borjesson-Hanson A, Viitanen M, Kalimo H, Deramecourt V, Oakley AE, Kalaria RN.

Neuropathol Appl Neurobiol. 2016 Feb;42(2):194-209. doi: 10.1111/nan.12248. Epub 2015 Jun 17.

5.

No cardiomyopathy in X-linked myopathy with excessive autophagy.

Saraste A, Koskenvuo JW, Airaksinen J, Ramachandran N, Munteanu I, Udd B, Huovinen S, Kalimo H, Minassian BA.

Neuromuscul Disord. 2015 Jun;25(6):485-7. doi: 10.1016/j.nmd.2015.03.003. Epub 2015 Mar 17.

PMID:
25845477
6.

Autophagy in neuropathology.

Minassian BA, Kalimo H.

Acta Neuropathol. 2015 Mar;129(3):333-5. doi: 10.1007/s00401-015-1396-1. No abstract available.

PMID:
25648862
7.

X-linked myopathy with excessive autophagy: a failure of self-eating.

Dowling JJ, Moore SA, Kalimo H, Minassian BA.

Acta Neuropathol. 2015 Mar;129(3):383-90. doi: 10.1007/s00401-015-1393-4. Epub 2015 Feb 3. Review.

PMID:
25644398
8.

CADASIL and CARASIL.

Tikka S, Baumann M, Siitonen M, Pasanen P, Pöyhönen M, Myllykangas L, Viitanen M, Fukutake T, Cognat E, Joutel A, Kalimo H.

Brain Pathol. 2014 Sep;24(5):525-44. doi: 10.1111/bpa.12181. Review.

PMID:
25323668
9.

Regeneration of injured skeletal muscle after the injury.

Järvinen TA, Järvinen M, Kalimo H.

Muscles Ligaments Tendons J. 2014 Feb 24;3(4):337-45. eCollection 2013 Oct.

10.

The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated Aβ.

Kalimo H, Lalowski M, Bogdanovic N, Philipson O, Bird TD, Nochlin D, Schellenberg GD, Brundin R, Olofsson T, Soliymani R, Baumann M, Wirths O, Bayer TA, Nilsson LN, Basun H, Lannfelt L, Ingelsson M.

Acta Neuropathol Commun. 2013 Sep 10;1:60. doi: 10.1186/2051-5960-1-60.

11.

Relationships between white matter hyperintensities, cerebral amyloid angiopathy and dementia in a population-based sample of the oldest old.

Tanskanen M, Kalaria RN, Notkola IL, Mäkelä M, Polvikoski T, Myllykangas L, Sulkava R, Kalimo H, Paetau A, Scheltens P, Barkhof F, van Straaten E, Erkinjuntti T.

Curr Alzheimer Res. 2013 Dec;10(10):1090-7.

PMID:
24156259
12.

White matter degeneration with Unverricht-Lundborg progressive myoclonus epilepsy: a translational diffusion-tensor imaging study in patients and cystatin B-deficient mice.

Manninen O, Koskenkorva P, Lehtimäki KK, Hyppönen J, Könönen M, Laitinen T, Kalimo H, Kopra O, Kälviäinen R, Gröhn O, Lehesjoki AE, Vanninen R.

Radiology. 2013 Oct;269(1):232-9. doi: 10.1148/radiol.13122458. Epub 2013 Jun 20.

PMID:
23788720
13.

Polymorphonuclear neutrophil infiltration into ischemic infarctions: myth or truth?

Kalimo H, del Zoppo GJ, Paetau A, Lindsberg PJ.

Acta Neuropathol. 2013 Mar;125(3):313-6. doi: 10.1007/s00401-013-1098-5. No abstract available.

PMID:
23417713
14.

Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases.

Craggs LJ, Hagel C, Kuhlenbaeumer G, Borjesson-Hanson A, Andersen O, Viitanen M, Kalimo H, McLean CA, Slade JY, Hall RA, Oakley AE, Yamamoto Y, Deramecourt V, Kalaria RN.

Brain Pathol. 2013 Sep;23(5):547-57. doi: 10.1111/bpa.12041. Epub 2013 Mar 8.

PMID:
23387519
15.

Monoclonal antibodies selective for α-synuclein oligomers/protofibrils recognize brain pathology in Lewy body disorders and α-synuclein transgenic mice with the disease-causing A30P mutation.

Fagerqvist T, Lindström V, Nordström E, Lord A, Tucker SM, Su X, Sahlin C, Kasrayan A, Andersson J, Welander H, Näsström T, Holmquist M, Schell H, Kahle PJ, Kalimo H, Möller C, Gellerfors P, Lannfelt L, Bergström J, Ingelsson M.

J Neurochem. 2013 Jul;126(1):131-44. doi: 10.1111/jnc.12175. Epub 2013 Feb 27.

16.

VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy.

Ramachandran N, Munteanu I, Wang P, Ruggieri A, Rilstone JJ, Israelian N, Naranian T, Paroutis P, Guo R, Ren ZP, Nishino I, Chabrol B, Pellissier JF, Minetti C, Udd B, Fardeau M, Tailor CS, Mahuran DJ, Kissel JT, Kalimo H, Levy N, Manolson MF, Ackerley CA, Minassian BA.

Acta Neuropathol. 2013 Mar;125(3):439-57. doi: 10.1007/s00401-012-1073-6. Epub 2013 Jan 12.

PMID:
23315026
17.

CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cells.

Tikka S, Ng YP, Di Maio G, Mykkänen K, Siitonen M, Lepikhova T, Pöyhönen M, Viitanen M, Virtanen I, Kalimo H, Baumann M.

J Cereb Blood Flow Metab. 2012 Dec;32(12):2171-80. doi: 10.1038/jcbfm.2012.123. Epub 2012 Sep 5.

18.

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene.

Kousi M, Anttila V, Schulz A, Calafato S, Jakkula E, Riesch E, Myllykangas L, Kalimo H, Topçu M, Gökben S, Alehan F, Lemke JR, Alber M, Palotie A, Kopra O, Lehesjoki AE.

J Med Genet. 2012 Jun;49(6):391-9. doi: 10.1136/jmedgenet-2012-100859.

19.

Prolonged myalgia in Sindbis virus infection: case description and in vitro infection of myotubes and myoblasts.

Sane J, Kurkela S, Desdouits M, Kalimo H, Mazalrey S, Lokki ML, Vaheri A, Helve T, Törnwall J, Huerre M, Butler-Browne G, Ceccaldi PE, Gessain A, Vapalahti O.

J Infect Dis. 2012 Aug 1;206(3):407-14. doi: 10.1093/infdis/jis358. Epub 2012 May 21.

PMID:
22615321
20.

The Arctic amyloid-β precursor protein (AβPP) mutation results in distinct plaques and accumulation of N- and C-truncated Aβ.

Philipson O, Lord A, Lalowski M, Soliymani R, Baumann M, Thyberg J, Bogdanovic N, Olofsson T, Tjernberg LO, Ingelsson M, Lannfelt L, Kalimo H, Nilsson LN.

Neurobiol Aging. 2012 May;33(5):1010.e1-13. doi: 10.1016/j.neurobiolaging.2011.10.022. Epub 2011 Nov 26.

PMID:
22118948
21.

The significance of latissimus dorsi flap innervation in delayed breast reconstruction: a prospective randomized study-magnetic resonance imaging and histologic findings.

Kääriäinen M, Giordano S, Kauhanen S, Lääperi AL, Mattila P, Helminen M, Kalimo H, Kuokkanen H.

Plast Reconstr Surg. 2011 Dec;128(6):637e-45e. doi: 10.1097/PRS.0b013e318230c544.

PMID:
22094764
22.

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.

Renton AE, Majounie E, Waite A, Simón-Sánchez J, Rollinson S, Gibbs JR, Schymick JC, Laaksovirta H, van Swieten JC, Myllykangas L, Kalimo H, Paetau A, Abramzon Y, Remes AM, Kaganovich A, Scholz SW, Duckworth J, Ding J, Harmer DW, Hernandez DG, Johnson JO, Mok K, Ryten M, Trabzuni D, Guerreiro RJ, Orrell RW, Neal J, Murray A, Pearson J, Jansen IE, Sondervan D, Seelaar H, Blake D, Young K, Halliwell N, Callister JB, Toulson G, Richardson A, Gerhard A, Snowden J, Mann D, Neary D, Nalls MA, Peuralinna T, Jansson L, Isoviita VM, Kaivorinne AL, Hölttä-Vuori M, Ikonen E, Sulkava R, Benatar M, Wuu J, Chiò A, Restagno G, Borghero G, Sabatelli M; ITALSGEN Consortium, Heckerman D, Rogaeva E, Zinman L, Rothstein JD, Sendtner M, Drepper C, Eichler EE, Alkan C, Abdullaev Z, Pack SD, Dutra A, Pak E, Hardy J, Singleton A, Williams NM, Heutink P, Pickering-Brown S, Morris HR, Tienari PJ, Traynor BJ.

Neuron. 2011 Oct 20;72(2):257-68. doi: 10.1016/j.neuron.2011.09.010. Epub 2011 Sep 21.

23.

Prevalence and severity of cerebral amyloid angiopathy: a population-based study on very elderly Finns (Vantaa 85+).

Tanskanen M, Mäkelä M, Myllykangas L, Notkola IL, Polvikoski T, Sulkava R, Kalimo H, Paetau A.

Neuropathol Appl Neurobiol. 2012 Jun;38(4):329-36. doi: 10.1111/j.1365-2990.2011.01219.x.

PMID:
21916927
24.

Gelsolin co-occurs with Lewy bodies in vivo and accelerates α-synuclein aggregation in vitro.

Welander H, Bontha SV, Näsström T, Karlsson M, Nikolajeff F, Danzer K, Kostka M, Kalimo H, Lannfelt L, Ingelsson M, Bergström J.

Biochem Biophys Res Commun. 2011 Aug 19;412(1):32-8. doi: 10.1016/j.bbrc.2011.07.027. Epub 2011 Jul 21.

PMID:
21798243
25.

APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysis.

Peuralinna T, Tanskanen M, Mäkelä M, Polvikoski T, Paetau A, Kalimo H, Sulkava R, Hardy J, Lai SL, Arepalli S, Hernandez D, Traynor BJ, Singleton A, Tienari PJ, Myllykangas L.

J Alzheimers Dis. 2011;26(2):377-85. doi: 10.3233/JAD-2011-102049.

26.

Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease.

Arboleda-Velasquez JF, Manent J, Lee JH, Tikka S, Ospina C, Vanderburg CR, Frosch MP, Rodríguez-Falcón M, Villen J, Gygi S, Lopera F, Kalimo H, Moskowitz MA, Ayata C, Louvi A, Artavanis-Tsakonas S.

Proc Natl Acad Sci U S A. 2011 May 24;108(21):E128-35. doi: 10.1073/pnas.1101964108. Epub 2011 May 9.

27.

Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus.

Hackman P, Sandell S, Sarparanta J, Luque H, Huovinen S, Palmio J, Paetau A, Kalimo H, Mahjneh I, Udd B.

Neuromuscul Disord. 2011 May;21(5):338-44. doi: 10.1016/j.nmd.2011.02.008. Epub 2011 Mar 3.

PMID:
21376592
28.

Review: molecular genetics and pathology of hereditary small vessel diseases of the brain.

Yamamoto Y, Craggs L, Baumann M, Kalimo H, Kalaria RN.

Neuropathol Appl Neurobiol. 2011 Feb;37(1):94-113. doi: 10.1111/j.1365-2990.2010.01147.x. Review.

PMID:
21062344
29.

Identification of low molecular weight pyroglutamate A{beta} oligomers in Alzheimer disease: a novel tool for therapy and diagnosis.

Wirths O, Erck C, Martens H, Harmeier A, Geumann C, Jawhar S, Kumar S, Multhaup G, Walter J, Ingelsson M, Degerman-Gunnarsson M, Kalimo H, Huitinga I, Lannfelt L, Bayer TA.

J Biol Chem. 2010 Dec 31;285(53):41517-24. doi: 10.1074/jbc.M110.178707. Epub 2010 Oct 22.

30.

Bedside diagnosis of rippling muscle disease in CAV3 p.A46T mutation carriers.

Sundblom J, Stålberg E, Osterdahl M, Rücker F, Montelius M, Kalimo H, Nennesmo I, Islander G, Smits A, Dahl N, Melberg A.

Muscle Nerve. 2010 Jun;41(6):751-7. doi: 10.1002/mus.21589.

PMID:
20229577
31.

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.

Vihola A, Bachinski LL, Sirito M, Olufemi SE, Hajibashi S, Baggerly KA, Raheem O, Haapasalo H, Suominen T, Holmlund-Hampf J, Paetau A, Cardani R, Meola G, Kalimo H, Edström L, Krahe R, Udd B.

Acta Neuropathol. 2010 Apr;119(4):465-79. doi: 10.1007/s00401-010-0637-6. Epub 2010 Jan 12.

32.

alpha-Synuclein pathology in the spinal cord autonomic nuclei associates with alpha-synuclein pathology in the brain: a population-based Vantaa 85+ study.

Oinas M, Paetau A, Myllykangas L, Notkola IL, Kalimo H, Polvikoski T.

Acta Neuropathol. 2010 Jun;119(6):715-22. doi: 10.1007/s00401-009-0629-6.

PMID:
20037761
33.

Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onset.

Melberg A, Kretz C, Kalimo H, Wallgren-Pettersson C, Toussaint A, Böhm J, Stålberg E, Laporte J.

Neuromuscul Disord. 2010 Jan;20(1):53-6. doi: 10.1016/j.nmd.2009.10.006. Epub 2009 Nov 22.

PMID:
19932619
34.

Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden.

Suhr OB, Andersen O, Aronsson T, Jonasson J, Kalimo H, Lundahl C, Lundgren HE, Melberg A, Nyberg J, Olsson M, Sandberg A, Westermark P.

Amyloid. 2009 Dec;16(4):208-14. doi: 10.3109/13506120903421587.

PMID:
19922332
35.

Pyroglutamate Abeta pathology in APP/PS1KI mice, sporadic and familial Alzheimer's disease cases.

Wirths O, Bethge T, Marcello A, Harmeier A, Jawhar S, Lucassen PJ, Multhaup G, Brody DL, Esparza T, Ingelsson M, Kalimo H, Lannfelt L, Bayer TA.

J Neural Transm (Vienna). 2010 Jan;117(1):85-96. doi: 10.1007/s00702-009-0314-x. Epub 2009 Oct 13.

36.

Neuropathologic findings of dementia with lewy bodies (DLB) in a population-based Vantaa 85+ study.

Oinas M, Polvikoski T, Sulkava R, Myllykangas L, Juva K, Notkola IL, Rastas S, Niinistö L, Kalimo H, Paetau A.

J Alzheimers Dis. 2009;18(3):677-89. doi: 10.3233/JAD-2009-1169.

PMID:
19625740
37.

VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification.

Ramachandran N, Munteanu I, Wang P, Aubourg P, Rilstone JJ, Israelian N, Naranian T, Paroutis P, Guo R, Ren ZP, Nishino I, Chabrol B, Pellissier JF, Minetti C, Udd B, Fardeau M, Tailor CS, Mahuran DJ, Kissel JT, Kalimo H, Levy N, Manolson MF, Ackerley CA, Minassian BA.

Cell. 2009 Apr 17;137(2):235-46. doi: 10.1016/j.cell.2009.01.054. Retraction in: Cell. 2010 Sep 17;142(6):984.

38.

Different clinical phenotypes in monozygotic CADASIL twins with a novel NOTCH3 mutation.

Mykkänen K, Junna M, Amberla K, Bronge L, Kääriäinen H, Pöyhönen M, Kalimo H, Viitanen M.

Stroke. 2009 Jun;40(6):2215-8. doi: 10.1161/STROKEAHA.108.528661. Epub 2009 Apr 16.

PMID:
19372454
39.

Absence of polysialylated NCAM is an unfavorable prognostic phenotype for advanced stage neuroblastoma.

Korja M, Jokilammi A, Salmi TT, Kalimo H, Pelliniemi TT, Isola J, Rantala I, Haapasalo H, Finne J.

BMC Cancer. 2009 Feb 17;9:57. doi: 10.1186/1471-2407-9-57.

40.

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.

Tikka S, Mykkänen K, Ruchoux MM, Bergholm R, Junna M, Pöyhönen M, Yki-Järvinen H, Joutel A, Viitanen M, Baumann M, Kalimo H.

Brain. 2009 Apr;132(Pt 4):933-9. doi: 10.1093/brain/awn364. Epub 2009 Jan 27.

41.

MR imaging characteristics and neuropathology of the spinal cord in adult-onset autosomal dominant leukodystrophy with autonomic symptoms.

Sundblom J, Melberg A, Kalimo H, Smits A, Raininko R.

AJNR Am J Neuroradiol. 2009 Feb;30(2):328-35. doi: 10.3174/ajnr.A1354. Epub 2008 Oct 22.

42.

Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.

Skoglund L, Brundin R, Olofsson T, Kalimo H, Ingvast S, Blom ES, Giedraitis V, Ingelsson M, Lannfelt L, Basun H, Glaser A.

Neurogenetics. 2009 Feb;10(1):27-34. doi: 10.1007/s10048-008-0155-z. Epub 2008 Oct 15.

PMID:
18855025
43.

Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family.

Eeg-Olofsson O, Kalimo H, Eeg-Olofsson KE, Jagell S, Marklund L, Simonsson L, Dahl N.

Eur J Paediatr Neurol. 2008 Sep;12(5):404-7.

PMID:
18833644
44.

Decreased expression of antioxidant enzymes is associated with aggressive features in ependymomas.

Järvelä S, Nordfors K, Jansson M, Haapasalo J, Helén P, Paljärvi L, Kalimo H, Kinnula V, Soini Y, Haapasalo H.

J Neurooncol. 2008 Dec;90(3):283-91. doi: 10.1007/s11060-008-9658-6. Epub 2008 Aug 6.

PMID:
18682894
45.

Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein.

Peuralinna T, Oinas M, Polvikoski T, Paetau A, Sulkava R, Niinistö L, Kalimo H, Hernandez D, Hardy J, Singleton A, Tienari PJ, Myllykangas L.

Ann Neurol. 2008 Sep;64(3):348-52. doi: 10.1002/ana.21446.

PMID:
18661559
46.

Muscle paralysis and myosin loss in a patient with cancer cachexia.

Banduseela V, Ochala J, Lamberg K, Kalimo H, Larsson L.

Acta Myol. 2007 Dec;26(3):136-44.

47.

PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease.

Koivunen J, Verkkoniemi A, Aalto S, Paetau A, Ahonen JP, Viitanen M, Någren K, Rokka J, Haaparanta M, Kalimo H, Rinne JO.

Brain. 2008 Jul;131(Pt 7):1845-53. doi: 10.1093/brain/awn107. Epub 2008 Jun 25.

PMID:
18583368
48.

Notch signaling regulates platelet-derived growth factor receptor-beta expression in vascular smooth muscle cells.

Jin S, Hansson EM, Tikka S, Lanner F, Sahlgren C, Farnebo F, Baumann M, Kalimo H, Lendahl U.

Circ Res. 2008 Jun 20;102(12):1483-91. doi: 10.1161/CIRCRESAHA.107.167965. Epub 2008 May 15.

PMID:
18483410
49.

Heparan sulfate accumulation with Abeta deposits in Alzheimer's disease and Tg2576 mice is contributed by glial cells.

O'Callaghan P, Sandwall E, Li JP, Yu H, Ravid R, Guan ZZ, van Kuppevelt TH, Nilsson LN, Ingelsson M, Hyman BT, Kalimo H, Lindahl U, Lannfelt L, Zhang X.

Brain Pathol. 2008 Oct;18(4):548-61. doi: 10.1111/j.1750-3639.2008.00152.x. Epub 2008 Apr 11.

50.

A highly insoluble state of Abeta similar to that of Alzheimer's disease brain is found in Arctic APP transgenic mice.

Philipson O, Hammarström P, Nilsson KP, Portelius E, Olofsson T, Ingelsson M, Hyman BT, Blennow K, Lannfelt L, Kalimo H, Nilsson LN.

Neurobiol Aging. 2009 Sep;30(9):1393-405. doi: 10.1016/j.neurobiolaging.2007.11.022. Epub 2008 Jan 14.

PMID:
18192084

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