Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures
Stödberg, Tommy, McTague, Amy, Ruiz, Arnaud J., Hirata, Hiromi, Zhen, Juan, Long, Philip, Farabella, Irene, Meyer, Esther, Kawahara, Atsuo, Vassallo, Grace, Stivaros, Stavros M., Bjursell, Magnus K., Stranneheim, Henrik, Tigerschiöld, Stephanie, Persson, Bengt, Bangash, Iftikhar, Das, Krishna, Hughes, Deborah, Lesko, Nicole, Lundeberg, Joakim, Scott, Rod C., Poduri, Annapurna, Scheffer, Ingrid E., Smith, Holly, Gissen, Paul, Schorge, Stephanie, Reith, Maarten E. A., Topf, Maya, Kullmann, Dimitri M., Harvey, Robert J., Wedell, Anna, Kurian, Manju A.
Published in Nature communications (03.09.2015)
Published in Nature communications (03.09.2015)
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Journal Article
Childhood encephalitis in Sweden: Etiology, clinical presentation and outcome
Fowler, Å, Stödberg, T, Eriksson, M, Wickström, R
Published in European journal of paediatric neurology (01.11.2008)
Published in European journal of paediatric neurology (01.11.2008)
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Journal Article
De novo SCN1A mutations in migrating partial seizures of infancy
Carranza Rojo, D, Hamiwka, L, McMahon, J M, Dibbens, L M, Arsov, T, Suls, A, Stödberg, T, Kelley, K, Wirrell, E, Appleton, B, Mackay, M, Freeman, J L, Yendle, S C, Berkovic, S F, Bienvenu, T, De Jonghe, P, Thorburn, D R, Mulley, J C, Mefford, H C, Scheffer, I E
Published in Neurology (26.07.2011)
Published in Neurology (26.07.2011)
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Journal Article
MEG and navigated TMS jointly enable spatially accurate application of TMS therapy at the epileptic focus in pharmacoresistant epilepsy
Islam, Mominul, Westin, Karin, Carvalho, Ana, Eriksson, Mats, Lundvall, Mikael, Stödberg, Tommy, Adelöw, Cecilia, Lundqvist, Daniel, Andersen, Lau M., Lundstrom, Brian Nils, Cooray, Gerald
Published in Brain stimulation (01.09.2019)
Published in Brain stimulation (01.09.2019)
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Journal Article
Diagnosing epileptic seizures and epilepsy
Malmgren, Kristina, Stödberg, Tommy, Amandusson, Åsa, Strandberg, Maria
Published in Läkartidningen (21.05.2018)
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Published in Läkartidningen (21.05.2018)
Journal Article
Diagnostic pitfalls in vitamin B6‐dependent epilepsy caused by mutations in the PLPBP gene
Jensen, Kristian Vestergaard, Frid, Maria, Stödberg, Tommy, Barbaro, Michela, Wedell, Anna, Christensen, Mette, Bak, Mads, Ek, Jakob, Madsen, Camilla Gøbel, Darin, Niklas, Grønborg, Sabine
Published in JIMD reports (01.11.2019)
Published in JIMD reports (01.11.2019)
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Journal Article
A case of diffuse leptomeningeal oligodendrogliomatosis associated with HHV-6 variant A
Stödberg, T, Deniz, Y, Esteitie, N, Jacobsson, B, Mousavi-Jazi, M, Dahl, H, Zweygberg Wirgart, B, Grillner, L, Linde, A
Published in Neuropediatrics (01.10.2002)
Published in Neuropediatrics (01.10.2002)
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Journal Article
A de novo gain-of-function mutation in SCN11A causes loss of pain perception
Leipold, Enrico, Liebmann, Lutz, Korenke, G Christoph, Heinrich, Theresa, Gießelmann, Sebastian, Baets, Jonathan, Ebbinghaus, Matthias, Goral, R Oliver, Stödberg, Tommy, Hennings, J Christopher, Bergmann, Markus, Altmüller, Janine, Thiele, Holger, Wetzel, Andrea, Nürnberg, Peter, Timmerman, Vincent, De Jonghe, Peter, Blum, Robert, Schaible, Hans-Georg, Weis, Joachim, Heinemann, Stefan H, Hübner, Christian A, Kurth, Ingo
Published in Nature genetics (01.11.2013)
Published in Nature genetics (01.11.2013)
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Journal Article
Epilepsy syndromes, etiologies, and the use of next‐generation sequencing in epilepsy presenting in the first 2 years of life: A population‐based study
Stödberg, Tommy, Tomson, Torbjörn, Barbaro, Michela, Stranneheim, Henrik, Anderlid, Britt‐Marie, Carlsson, Sofia, Åmark, Per, Wedell, Anna
Published in Epilepsia (Copenhagen) (01.11.2020)
Published in Epilepsia (Copenhagen) (01.11.2020)
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Journal Article
Unraveling GRIA1 neurodevelopmental disorders: Lessons learned from the p.(Ala636Thr) variant
Tvergaard, Nicolai Kohring, Tkemaladze, Tinatin, Stödberg, Tommy, Kvarnung, Malin, Tatton‐Brown, Katrina, Baralle, Diana, Tümer, Zeynep, Bayat, Allan
Published in Clinical genetics (01.10.2024)
Published in Clinical genetics (01.10.2024)
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Journal Article
Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcome
Mills, Philippa B., Camuzeaux, Stephane S.M., Footitt, Emma J., Mills, Kevin A., Gissen, Paul, Fisher, Laura, Das, Krishna B., Varadkar, Sophia M., Zuberi, Sameer, McWilliam, Robert, Stödberg, Tommy, Plecko, Barbara, Baumgartner, Matthias R., Maier, Oliver, Calvert, Sophie, Riney, Kate, Wolf, Nicole I., Livingston, John H., Bala, Pronab, Morel, Chantal F., Feillet, François, Raimondi, Francesco, Del Giudice, Ennio, Chong, W. Kling, Pitt, Matthew, Clayton, Peter T.
Published in Brain (London, England : 1878) (01.05.2014)
Published in Brain (London, England : 1878) (01.05.2014)
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Journal Article
A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT
Kvarnung, Malin, Nilsson, Daniel, Lindstrand, Anna, Korenke, G Christoph, Chiang, Samuel C C, Blennow, Elisabeth, Bergmann, Markus, Stödberg, Tommy, Mäkitie, Outi, Anderlid, Britt-Marie, Bryceson, Yenan T, Nordenskjöld, Magnus, Nordgren, Ann
Published in Journal of medical genetics (01.08.2013)
Published in Journal of medical genetics (01.08.2013)
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Journal Article
Benign paroxysmal torticollis of infancy does not lead to neurological sequelae
Danielsson, Annika, Anderlid, Britt‐Marie, Stödberg, Tommy, Lagerstedt‐Robinson, Kristina, Klackenberg Arrhenius, Eva, Tedroff, Kristina
Published in Developmental medicine and child neurology (01.12.2018)
Published in Developmental medicine and child neurology (01.12.2018)
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Journal Article
Long-term outcomes of acute encephalitis in childhood
Fowler, Asa, Stödberg, Tommy, Eriksson, Margareta, Wickström, Ronny
Published in Pediatrics (Evanston) (01.10.2010)
Published in Pediatrics (Evanston) (01.10.2010)
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Journal Article
SLC25A22 is a novel gene for migrating partial seizures in infancy
Poduri, Annapurna, Heinzen, Erin L., Chitsazzadeh, Vida, Lasorsa, Francesco Massimo, Elhosary, P. Christina, LaCoursiere, Christopher M., Martin, Emilie, Yuskaitis, Christopher J., Hill, Robert Sean, Atabay, Kutay Deniz, Barry, Brenda, Partlow, Jennifer N., Bashiri, Fahad A., Zeidan, Radwan M., Elmalik, Salah A., Kabiraj, Mohammad M. U., Kothare, Sanjeev, Stödberg, Tommy, McTague, Amy, Kurian, Manju A., Scheffer, Ingrid E., Barkovich, A. James, Palmieri, Ferdinando, Salih, Mustafa A., Walsh, Christopher A.
Published in Annals of neurology (01.12.2013)
Published in Annals of neurology (01.12.2013)
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