jeaneko

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Publications

  • Dahl-Hansen, Eline; Koht, Jeanette & Syvertsen, Marte Roa (2019). Epilepsy at different ages-Etiologies in a Norwegian population. Epilepsia Open.  ISSN 2470-9239.  4(1), s 176- 181 . doi: 10.1002/epi4.12292 Full text in Research Archive.
  • Iqbal, Zafar; Koht, Jeanette; Pihlstrøm, Lasse; Henriksen, Sandra Pilar; Cappelletti, Chiara; Russell, Michael Bjørn; de Souza, Osmar Norberto; Skogseid, Inger Marie & Toft, Mathias (2019). Missense mutations in DYT-TOR1A dystonia. Neurology: Genetics.  ISSN 2376-7839.  5:e343(4), s 1- 6 . doi: 10.1212/NXG.0000000000000343 Full text in Research Archive.
  • Landmark, Cecilie Johannessen; Fløgstad, Ida; Baftiu, Arton; Syvertsen, Marte Roa; Enger, Ulla Helene; Koht, Jeanette & Johannessen, Svein Ivar (2019). Long-term follow-up with therapeutic drug monitoring of antiepileptic drugs in patients with juvenile myoclonic epilepsy. Epilepsy Research.  ISSN 0920-1211.  155, s 1- 8 . doi: 10.1016/j.eplepsyres.2019.05.016
  • Landmark, Cecilie Johannessen; Fløgstad, Ida; Syvertsen, Marte Roa; Baftiu, Arton; Enger, Ulla Helene; Koht, Jeanette & Johannessen, Svein Ivar (2019). Treatment and challenges with antiepileptic drugs in patients with juvenile myoclonic epilepsy. Epilepsy & Behavior.  ISSN 1525-5050.  98, s 110- 116 . doi: 10.1016/j.yebeh.2019.05.021
  • Rydning, Siri Lynne; Koht, Jeanette; Sheng, Ying; Sowa, Piotr; Hjorthaug, Hanne Sagsveen; Wedding, Iselin Marie; ERICHSEN, ANNE KJERSTI; Hynås, Inger Anette; Backe, Paul Hoff; Tallaksen, Chantal; Vigeland, Magnus Dehli & Selmer, Kaja Kristine (2019). Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis. Brain.  ISSN 0006-8950.  142:e12(4), s 1- 5 . doi: 10.1093/brain/awz041 Full text in Research Archive.
  • Stenshorne, Ida; Rasmussen, Magnhild; Salvanos, Panagiotis; Tallaksen, Chantal; Bindoff, Laurence & Koht, Jeanette (2019). Fever-related ataxia: A case report of CAPOS syndrome. Cerebellum & ataxias.  ISSN 2053-8871.  6:2, s 1- 5 . doi: 10.1186/s40673-019-0096-3 Full text in Research Archive.
  • Syvertsen, Marte Roa; Fløgstad, Ida; Enger, Ulla Helene; Landmark, Cecilie Johannessen & Koht, Jeanette (2019). Antiepileptic drug withdrawal in juvenile myoclonic epilepsy. Acta Neurologica Scandinavica.  ISSN 0001-6314.  139(2), s 192- 198 . doi: 10.1111/ane.13042
  • Syvertsen, Marte Roa; Selmer, Kaja Kristine; Enger, Ulla Helene; Nakken, Karl Otto; Pal, Deb K.; Smith, Anna & Koht, Jeanette (2019). Psychosocial complications in juvenile myoclonic epilepsy. Epilepsy & Behavior.  ISSN 1525-5050.  90, s 122- 128 . doi: 10.1016/j.yebeh.2018.11.022 Show summary
  • Giltvedt, Kaja; Fossmo, Hanne Ludt & Koht, Jeanette (2018). Fysioterapi ved arvelig ataksi. Fysioterapeuten.  ISSN 0016-3384.  85(6), s 22- 27
  • Randby, Hans; Salvador, Cathrin Lytomt; Oppebøen, Mari; Skogseid, Inger Marie & Koht, Jeanette (2018). Doparesponsive dystonier. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  138(19), s 1842- 1847 . doi: 10.4045/tidsskr.17.0595
  • Sjaastad, Ottar; Blau, Nenad; Rydning, Siri Lynne; Peters, Verena; Rødningen, Olaug Kristin; Stray-Pedersen, Asbjørg; Krossnes, Bård Kronen; Tallaksen, Chantal & Koht, Jeanette (2018). Homocarnosinosis: A historical update and findings in the SPG11 gene. Acta Neurologica Scandinavica.  ISSN 0001-6314.  138(3), s 245- 250 . doi: 10.1111/ane.12949
  • Hoem, Gry & Koht, Jeanette (2017). Fragilt X-assosiert tremor-ataksi-syndrom. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  137(20) . doi: 10.4045/tidsskr.17.0317
  • Iqbal, Zafar; Rydning, Siri Lynne; Wedding, Iselin Marie; Koht, Jeanette; Pihlstrøm, Lasse; Rengmark, Aina Sylvia Haugen; Henriksen, Sandra Pilar; Tallaksen, Chantal & Toft, Harald Mathias Strøm (2017). Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia. PLOS ONE.  ISSN 1932-6203.  12:e0174667(3), s 1- 19 . doi: 10.1371/journal.pone.0174667 Full text in Research Archive.
  • Koht, Jeanette; Hansen, Anniken; Blom, Johanna & Elvik, Anette Holmelid (2017). Dystoni: klassifikasjon, årsak og behandling. Fysioterapeuten.  ISSN 0016-3384.  84(1), s 24- 28
  • Syvertsen, Marte Roa; Hellum, Morten Kristoffer; Hansen, Gunnar; Edland, Astrid; Nakken, Karl Otto; Selmer, Kaja Kristine & Koht, Jeanette (2017). Prevalence of juvenile myoclonic epilepsy in people <30 years of age—A population-based study in Norway. Epilepsia.  ISSN 0013-9580.  58(1), s 105- 112 . doi: 10.1111/epi.13613
  • Ødemark, Elin & Koht, Jeanette (2017). Mannen som falt om i åkeren. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  137(12) . doi: 10.4045/tidsskr.16.1011
  • Koht, Jeanette; Løstegaard, Sven Olav; Wedding, Iselin Marie; Vidailhet, Marie; Louha, Malek & Tallaksen, Chantal (2016). Benign hereditary chorea, not only chorea: a family case presentation. Cerebellum & ataxias.  ISSN 2053-8871.  3 . doi: 10.1186/s40673-016-0041-7
  • Rydning, Siri Lynne; Wedding, Iselin Marie; Koht, Jeanette; Chawla, Maninder Singh; Øye, Ane-Marte; Sheng, Ying; Vigeland, Magnus Dehli; Selmer, Kaja Kristine & Tallaksen, Chantal (2016). A founder mutation p.H701P identified as a major cause of SPG7 in Norway. European Journal of Neurology.  ISSN 1351-5101.  23(4), s 763- 771 . doi: 10.1111/ene.12937 Full text in Research Archive. Show summary
  • Syvertsen, Marte; Koht, Jeanette & Nakken, Karl Otto (2015). Forekomst av epilepsi i de nordiske landene :. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  135(18), s 1641- 1645 . doi: 10.4045/tidsskr.15.0454
  • Syvertsen, Marte; Nakken, Karl Otto; Edland, Astrid; Hansen, Gunnar; Hellum, Morten Kristoffer & Koht, Jeanette (2015). Prevalence and etiology of epilepsy in a Norwegian county - A population based study. Epilepsia.  ISSN 0013-9580.  56(5), s 699- 706 . doi: 10.1111/epi.12972
  • Tesson, Christelle; Koht, Jeanette & Stevanin, Giovanni (2015). Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology. Human Genetics.  ISSN 0340-6717.  134, s 511- 538 . doi: 10.1007/s00439-015-1536-7
  • Heimdal, Ketil Riddervold; Sanchez Guixe, Monica; Aukrust, Ingvild; Bollerslev, Jens; Bruland, Ove; Jablonski, Greg; ERICHSEN, ANNE KJERSTI; Gude, Einar; Koht, Jeanette; Erdal, Sigrid; Fiskerstrand, Torunn; Haukanes, Bjørn Ivar; Boman, Helge; Bjørkhaug, Lise; Tallaksen, Chantal; Knappskog, Per & Johansson, Stefan (2014). STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity. Orphanet Journal of Rare Diseases.  ISSN 1750-1172.  9:146 . doi: 10.1186/s13023-014-0146-0 Full text in Research Archive.
  • Koht, Jeanette; Rengmark, Aina Sylvia Haugen; Opladen, Thomas; Bjørnarå, Kari Anne; Selberg, Tore; Tallaksen, Chantal; Blau, N. & Toft, Mathias (2014). Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene. Acta Neurologica Scandinavica.  ISSN 0001-6314.  129(198), s 7- 12 . doi: 10.1111/ane.12230
  • Wedding, Iselin Marie; Koht, Jeanette; Tran, Gia Tuong Thi; Misceo, Doriana; Selmer, Kaja Kristine; Holmgren, Asbjørn; Frengen, Eirik; Bindoff, Laurence; Tallaksen, Chantal & Tzoulis, Charalampos (2014). Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions. PLOS ONE.  ISSN 1932-6203.  9(1) . doi: 10.1371/journal.pone.0086340 Full text in Research Archive.
  • Wedding, Iselin Marie; Koht, Jeanette; Dietrichs, Espen; Landrø, Nils Inge & Tallaksen, Chantal (2013). Cognition is only minimally impaired in Spinocerebellar ataxia type 14 (SCA14): a neuropsychological study of ten Norwegian subjects compared to intrafamilial controls and population norm. BMC Neurology.  ISSN 1471-2377.  13:186 . doi: 10.1186/1471-2377-13-186 Full text in Research Archive.
  • Gras, Domtille; Jonard, Laurence; Roze, Emmanuel; Chantot-Bastaraud, Sandra; Koht, Jeanette; Motte, Jacques; Rodriguez, Diana; Louha, Malek; Caubel, Isabelle; Kemlin, Isabelle; Lion-Francois, Laurence; Goizet, Cyril; Guillot, Loic; Moutard, Marie-Laure; Epaud, Ralph; Héron, Bénédicte; Charles, Perrine; Tallot, Marilyn; Camuzat, Agnès; Durr, Alexandra; Polak, Michel; Devos, David; Sanlaville, Damien; Vuillaume, Isabelle; de Villemeur, Thierry B.; Vidailhet, Marie & Doummar, Diane (2012). Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene. Journal of Neurology, Neurosurgery and Psychiatry.  ISSN 0022-3050.  83(10), s 956- 962 . doi: 10.1136/jnnp-2012-302505
  • Koht, Jeanette; Stevanin, G; Durr, A; Mundwiller, E; Brice, A & Tallaksen, Chantal (2012). SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene. Acta Neurologica Scandinavica.  ISSN 0001-6314.  125(2), s 116- 122 . doi: 10.1111/j.1600-0404.2011.01504.x
  • Koht, Jeanette; Tallaksen, Chantal & ERICHSEN, ANNE KJERSTI (2010). Kapitell om ataksier og spastiske parapareser, I: Leif Gjerstad; Eirik Helseth & Terje Rootwelt (red.),  Nevrologi og nevrokirurgi. Fra barn til voksen. 5.utgave.  Forlaget Vett & Viten.  ISBN 978-82-412-0686-3.  Arvelige ataksier og spastiske parapareser.
  • Anheim, M; Monga, B; Fleury, M; Charles, P; Barbot, C; Salih, M; Delaunoy, JP; Fritsch, M; Arning, L; Synofzik, M; Schols, L; Sequeiros, J; Goizet, C; Marelli, C; Le Ber, I; Koht, Jeanette Aimee; Gazulla, J; De Bleecker, J; Mukhtar, M; Drouot, N; Ali-Pacha, L; Benhassine, T; Chbicheb, M; M'Zahem, A; Hamri, A; Chabrol, B; Pouget, J; Murphy, R; Watanabe, M; Coutinho, P; Tazir, M; Durr, A; Brice, A; Tranchant, C & Koenig, M (2009). Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. Brain.  ISSN 0006-8950.  132, s 2688- 2698 . doi: 10.1093/brain/awp211
  • ERICHSEN, ANNE KJERSTI; Koht, Jeanette; Stray-Pedersen, Asbjørg; Abdelnoor, Michael & Tallaksen, Chantal (2009). Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study. Brain.  ISSN 0006-8950.  132, s 1577- 1588 . doi: 10.1093/brain/awp056
  • Koht, Jeanette Aimee; Bjornara, KA; Jørum, Ellen & Tallaksen, Chantal (2009). Ataxia with vitamin E deficiency in southeast Norway, case report. Acta Neurologica Scandinavica.  ISSN 0001-6314.  120, s 42- 45
  • Koht, Jeanette Aimee & Tallaksen, Chantal (2007). Cerebellar ataxia in the eastern and southern parts of Norway. Acta Neurologica Scandinavica.  ISSN 0001-6314.  115

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  • Fløgstad, Ida; Syvertsen, Marte Roa; Enger, Ulla Helene; Koht, Jeanette & Landmark, Cecilie Johannessen (2018). Monitorering av pasienter med juvenil myoklonus epilepsi.
  • Fløgstad, Ida; Syvertsen, Marte Roa; Enger, Ulla Helene; Koht, Jeanette & Landmark, Cecilie Johannessen (2018). Monitoring of pharmacological treatment of patients with juvenile myoclonus epilepsy.
  • Fløgstad, Ida; Syvertsen, Marte Roa; Enger, Ulla Helene; Koht, Jeanette & Landmark, Cecilie Johannessen (2018). Oppfølging av pasienter med JME.
  • ida, fløgstad; Syvertsen, Marte Roa; Koht, Jeanette & Landmark, Cecilie Johannessen (2018). Monitoring of pharmacological treatment of patients with juvenile myoclonus epilepsy.
  • Solberg, Marianne & Koht, Jeanette (2017). Oculogyric crises. Tremor and Other Hyperkinetic Movements.  ISSN 2160-8288.  7, s 1- 2 . doi: 10.7916/D85X2N2D
  • Gerstner, Thorsten; Moland, Siri & Koht, Jeanette (2015). Congenital mirror movements of the hands. Tidsskrift for Den norske legeforening.  ISSN 0029-2001.  135(20), s 1852- 1852 . doi: 10.4045/tidsskr.15.0733
  • Wedding, Iselin Marie; Koht, Jeanette; Landro, N. I. & Tallaksen, Chantal (2012). Cerebellum - more than motor control? Cognition in spinocerebellar ataxia type 14. European Journal of Neurology.  ISSN 1351-5101.  19, s 62- 62
  • Koht, Jeanette & Tallaksen, Chantal (2010). Two new autosomal dominant ataxia loci.
  • Koht, Jeanette (2009). Two Norwegian families with SCA14.
  • ERICHSEN, ANNE KJERSTI; Koht, Jeanette Aimee; Abdelnoor, M & Tallaksen, Chantal (2008). Hereditary spastic paraplegia in south-eastern Norway. European Journal of Neurology.  ISSN 1351-5101.  15, s 354- 354

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Published Aug. 31, 2016 10:08 AM - Last modified Sep. 16, 2016 3:34 PM