Door to thrombolysis: ER reorganization and reduced delays to acute stroke treatment
Lindsberg, P J, Häppölä, O, Kallela, M, Valanne, L, Kuisma, M, Kaste, M
Published in Neurology (25.07.2006)
Published in Neurology (25.07.2006)
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CT Angiographic Analysis of Carotid Artery Stenosis: Comparison of Manual Assessment, Semiautomatic Vessel Analysis, and Digital Subtraction Angiography
Silvennoinen, H.M, Ikonen, S, Soinne, L, Railo, M, Valanne, L
Published in American Journal of Neuroradiology (01.01.2007)
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Published in American Journal of Neuroradiology (01.01.2007)
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POLG1 manifestations in childhood
Isohanni, P, Hakonen, A H, Euro, L, Paetau, I, Linnankivi, T, Liukkonen, E, Wallden, T, Luostarinen, L, Valanne, L, Paetau, A, Uusimaa, J, Lönnqvist, T, Suomalainen, A, Pihko, H
Published in Neurology (01.03.2011)
Published in Neurology (01.03.2011)
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Combined use of non-invasive techniques for improved functional localization for a selected group of epilepsy surgery candidates
Vitikainen, A.-M., Lioumis, P., Paetau, R., Salli, E., Komssi, S., Metsähonkala, L., Paetau, A., Kičić, D., Blomstedt, G., Valanne, L., Mäkelä, J.P., Gaily, E.
Published in NeuroImage (Orlando, Fla.) (01.04.2009)
Published in NeuroImage (Orlando, Fla.) (01.04.2009)
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Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome
Götz, Alexandra, Isohanni, Pirjo, Pihko, Helena, Paetau, Anders, Herva, Riitta, Saarenpää-Heikkilä, Outi, Valanne, Leena, Marjavaara, Sanna, Suomalainen, Anu
Published in Brain (London, England : 1878) (01.11.2008)
Published in Brain (London, England : 1878) (01.11.2008)
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Teachers’ beliefs and practices related to mathematics instruction
Stipek, Deborah J, Givvin, Karen B, Salmon, Julie M, MacGyvers, Valanne L
Published in Teaching and teacher education (01.02.2001)
Published in Teaching and teacher education (01.02.2001)
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DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis
Isohanni, P, Linnankivi, T, Buzkova, J, Lönnqvist, T, Pihko, H, Valanne, L, Tienari, P J, Elovaara, I, Pirttilä, T, Reunanen, M, Koivisto, K, Marjavaara, S, Suomalainen, A
Published in Journal of medical genetics (01.01.2010)
Published in Journal of medical genetics (01.01.2010)
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Brain anomalies in 121 children with non-syndromic single suture craniosynostosis by MR imaging
Hukki, A, Koljonen, V, Karppinen, A, Valanne, L, Leikola, J
Published in European journal of paediatric neurology (01.11.2012)
Published in European journal of paediatric neurology (01.11.2012)
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CT Perfusion Identifies Increased Salvage of Tissue in Patients Receiving Intravenous Recombinant Tissue Plasminogen Activator within 3 Hours of Stroke Onset
Silvennoinen, H.M, Hamberg, L.M, Lindsberg, P.J, Valanne, L, Hunter, G.J
Published in American journal of neuroradiology : AJNR (01.06.2008)
Published in American journal of neuroradiology : AJNR (01.06.2008)
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Asymmetric laterality of Chiari type I malformation in patients with non-syndromic single-suture craniosynostosis
Karppinen, A., Koljonen, V., Valanne, L., Leikola, J.
Published in Acta neurochirurgica (01.11.2012)
Published in Acta neurochirurgica (01.11.2012)
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The evolution of cerebellar tonsillar herniation after cranial vault remodeling surgery
Leikola, J., Hukki, A., Karppinen, A., Valanne, L., Koljonen, V.
Published in Child's nervous system (01.10.2012)
Published in Child's nervous system (01.10.2012)
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P507: Predicting neurodevelopmental outcome of infants born <28 gestational weeks with magnetoencephalography and somatosensory evoked fields
Nevalainen, P, Pihko, E, Rahkonen, P, Lano, A, Vanhatalo, S, Andersson, S, Autti, T, Valanne, L, Metsaeranta, M, Lauronen, L
Published in Clinical neurophysiology (01.06.2014)
Published in Clinical neurophysiology (01.06.2014)
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Dominant encephalopathy mimicking mitochondrial disease
Lönnqvist, T, Isohanni, P, Valanne, L, Olli-Lähdesmäki, T, Suomalainen, A, Pihko, H
Published in Neurology (04.01.2011)
Published in Neurology (04.01.2011)
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Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease
Cormand, B, Pihko, H, Bayés, M, Valanne, L, Santavuori, P, Talim, B, Gershoni-Baruch, R, Ahmad, A, van Bokhoven, H, Brunner, H G, Voit, T, Topaloglu, H, Dobyns, W B, Lehesjoki, A E
Published in Neurology (24.04.2001)
Published in Neurology (24.04.2001)
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OP28 – 2809: Structural MRI, transcranial magnetic stimulation, magnetoencephalography and DTI tractography findings in relation to sensorimotor outcome after perinatal stroke
Lõo, S, Kuusela, L, Valanne, L, Vaalto, S, Nevalainen, P, Lauronen, L, Mäenpää, H
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Genetic Overlap between Holoprosencephaly and Kallmann Syndrome
Vaaralahti, K., Raivio, T., Koivu, R., Valanne, L., Laitinen, E.-M., Tommiska, J.
Published in Molecular syndromology (01.06.2012)
Published in Molecular syndromology (01.06.2012)
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Cerebroretinal microangiopathy with calcifications and cysts
Linnankivi, T, Valanne, L, Paetau, A, Alafuzoff, I, Hakumäki, J M, Kivelä, T, Lönnqvist, T, Mäkitie, O, Pääkkönen, L, Vainionpää, L, Vanninen, R, Herva, R, Pihko, H
Published in Neurology (24.10.2006)
Published in Neurology (24.10.2006)
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Increasing Contrast Agent Concentration Improves Enhancement in First-Pass CT Perfusion
Silvennoinen, H.M, Hamberg, L.M, Valanne, L, Hunter, G.J
Published in American journal of neuroradiology : AJNR (01.08.2007)
Published in American journal of neuroradiology : AJNR (01.08.2007)
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POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease
Diesen, C, Saarinen, A, Pihko, H, Rosenlew, C, Cormand, B, Dobyns, W B, Dieguez, J, Valanne, L, Joensuu, T, Lehesjoki, A-E
Published in Journal of medical genetics (01.10.2004)
Published in Journal of medical genetics (01.10.2004)
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