Search Results - "VALANNE, L"

Door to thrombolysis : ER reorganization and reduced delays to acute stroke treatment by LINDSBERG, P. J, HÄPPÖLÄ, O, KALLELA, M, VALANNE, L, KUISMA, M, KASTE, M

“…The authors reorganized the emergency room (ER) by moving CT to the ER and streamlining triage by prenotification by emergency medical services (EMS), which…”
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CT Angiographic Analysis of Carotid Artery Stenosis: Comparison of Manual Assessment, Semiautomatic Vessel Analysis, and Digital Subtraction Angiography by Silvennoinen, H.M, Ikonen, S, Soinne, L, Railo, M, Valanne, L

“…To compare multisection CT angiography (CTA) analyzed with source/maximum intensity projection (MIP) images as well as semiautomated vessel analysis software…”
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POLG1 manifestations in childhood by ISOHANNI, P, HAKONEN, A. H, UUSIMAA, J, LÖNNQVIST, T, SUOMALAINEN, A, PIHKO, H, EURO, L, PAETAU, I, LINNANKIVI, T, LIUKKONEN, E, WALLDEN, T, LUOSTARINEN, L, VALANNE, L, PAETAU, A

“…Mitochondrial DNA polymerase γ (POLG1) mutations in children often manifest as Alpers syndrome, whereas in adults, a common manifestation is mitochondrial…”
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Combined use of non-invasive techniques for improved functional localization for a selected group of epilepsy surgery candidates by 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.

“…Invasive cortical mapping is conventionally required for preoperative identification of epileptogenic and eloquent cortical regions before epilepsy surgery…”
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Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome by Götz, Alexandra, Isohanni, Pirjo, Pihko, Helena, Paetau, Anders, Herva, Riitta, Saarenpää-Heikkilä, Outi, Valanne, Leena, Marjavaara, Sanna, Suomalainen, Anu

“…Mitochondrial DNA depletion syndrome (MDS) is a severe recessively inherited disease of childhood. It manifests most often in infancy, is rapidly progressive…”
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Teachers’ beliefs and practices related to mathematics instruction by Stipek, Deborah J, Givvin, Karen B, Salmon, Julie M, MacGyvers, Valanne L

“…Beliefs and practices related to mathematics were assessed for 21 fourth- through sixth-grade teachers. At the beginning and the end of the school year…”
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DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis by 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

“…Leucoencephalopathy with brain stem and spinal cord involvement and high brain lactate (LBSL) was first defined by characteristic magnetic resonance imaging…”
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Brain anomalies in 121 children with non-syndromic single suture craniosynostosis by MR imaging by Hukki, A, Koljonen, V, Karppinen, A, Valanne, L, Leikola, J

“…Abstract Introduction The aim of this study was to evaluate prevalence of intracranial abnormalities in children with non-syndromic single suture…”
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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 by Silvennoinen, H.M, Hamberg, L.M, Lindsberg, P.J, Valanne, L, Hunter, G.J

“…In spite of the advent of thrombolytic therapy, CT-perfusion imaging is currently not fully used for clinical decision-making and not included in published…”
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Asymmetric laterality of Chiari type I malformation in patients with non-syndromic single-suture craniosynostosis by Karppinen, A., Koljonen, V., Valanne, L., Leikola, J.

“…Background Chiari type I malformation is a frequent incidental finding commonly associated with craniosynostosis. However, there seems to be a paucity of…”
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The evolution of cerebellar tonsillar herniation after cranial vault remodeling surgery by Leikola, J., Hukki, A., Karppinen, A., Valanne, L., Koljonen, V.

“…Purpose We sought to examine the pre- and postoperative changes of cerebellar tonsillar herniation by MR imaging in asymptomatic pediatric patients with…”
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P507: Predicting neurodevelopmental outcome of infants born <28 gestational weeks with magnetoencephalography and somatosensory evoked fields by Nevalainen, P, Pihko, E, Rahkonen, P, Lano, A, Vanhatalo, S, Andersson, S, Autti, T, Valanne, L, Metsaeranta, M, Lauronen, L

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DOMINANT ENCEPHALOPATHY MIMICKING MITOCHONDRIAL DISEASE by LÖNNQVIST, T, ISOHANNI, P, VALANNE, L, OLLI-LÄHDESMÄKI, T, SUOMALAINEN, A, PIHKO, H

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Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease by CORMAND, B, PIHKO, H, VOIT, T, TOPALOGLU, H, DOBYNS, W. B, LEHESJOKI, A.-E, BAYES, M, VALANNE, L, SANTAVUORI, P, TALIM, B, GERSHONI-BARUCH, R, AHMAD, A, VAN BOKHOVEN, H, BRUNNER, H. G

“…Three rare autosomal recessive disorders share the combination of congenital muscular dystrophy and brain malformations including a neuronal migration defect:…”
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OP28 – 2809: Structural MRI, transcranial magnetic stimulation, magnetoencephalography and DTI tractography findings in relation to sensorimotor outcome after perinatal stroke by Lõo, S, Kuusela, L, Valanne, L, Vaalto, S, Nevalainen, P, Lauronen, L, Mäenpää, H

“…Objective Despite the frequency and importance of sensorimotor deficits after perinatal stroke (PS), the correlation between brain damage and severity of…”
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Genetic Overlap between Holoprosencephaly and Kallmann Syndrome by Vaaralahti, K., Raivio, T., Koivu, R., Valanne, L., Laitinen, E.-M., Tommiska, J.

“…Patients with Kallmann syndrome (KS; congenital hypogonadotropic hypogonadism and decreased/absent sense of smell), septo-optic dysplasia (SOD), or…”
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Cerebroretinal microangiopathy with calcifications and cysts by LINNANKIVI, T, VALANNE, L, VANNINEN, R, HERVA, R, PIHKO, H, PAETAU, A, ALAFUZOFF, I, HAKUMÄKI, J. M, KIVELÄ, T, LÖNNQVIST, T, MÄKITIE, O, PÄÄKKÖNEN, L, VAINIONPÄÄ, L

“…Extensive cerebral calcifications and leukoencephalopathy have been reported in two rare disorders Coats plus and leukoencephalopathy with calcifications and…”
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Morphometric comparison of foramen magnum in non-syndromic craniosynostosis patients with or without Chiari I malformation by Leikola, J., Haapamäki, V., Karppinen, A., Koljonen, V., Hukki, J., Valanne, L., Koivikko, M.

“…Background In order to compare the morphometry of foramen magnum (FM) in a matched-pair study, in children with non-syndromic craniosynostosis with and without…”
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Increasing Contrast Agent Concentration Improves Enhancement in First-Pass CT Perfusion by Silvennoinen, H.M, Hamberg, L.M, Valanne, L, Hunter, G.J

“…Our aim was to evaluate whether increasing iodine concentration, at a constant total iodine dose, resulted in better brain tissue opacification in patients…”
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POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease by Diesen, C, Saarinen, A, Pihko, H, Rosenlew, C, Cormand, B, Dobyns, W B, Dieguez, J, Valanne, L, Joensuu, T, Lehesjoki, A-E

“…[...]the treatment of severely handicapped persons has improved during the past 30 years. Children, in whom hydrocephalus has been shunted early, myopia…”
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