Jeanette Koht
Position: PhD student, MD
Consultant in neurology at Vestre Viken Hospital Trust, Drammen

Author network for Jeanette Koht by COREMINE medical

Publications 2017

Hoem G, Koht J (2017)
Fragile X-associated tremor/ataxia syndrome
Tidsskr Nor Laegeforen, 137 (20)
PubMed 29094559

Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, Henriksen SP, Tallaksen CM, Toft M (2017)
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia
PLoS One, 12 (3), e0174667
PubMed 28362824

Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, Henriksen SP, Tallaksen CME, Toft M (2017)
Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia
PLoS One, 12 (10), e0186571
PubMed 29023604

Solberg M, Koht J (2017)
Oculogyric Crises
Tremor Other Hyperkinet Mov (N Y), 7, 491
PubMed 28975049

Ødemark E, Koht J (2017)
The man who collapsed in the field
Tidsskr Nor Laegeforen, 137 (12-13), 890-894
PubMed 28655247

Publications 2016

Koht J, Løstegaard SO, Wedding I, Vidailhet M, Louha M, Tallaksen CM (2016)
Benign hereditary chorea, not only chorea: a family case presentation
Cerebellum Ataxias, 3, 3
PubMed 26839702

Rydning SL, Wedding IM, Koht J, Chawla M, Øye AM, Sheng Y, Vigeland MD, Selmer KK, Tallaksen CM (2016)
A founder mutation p.H701P identified as a major cause of SPG7 in Norway
Eur J Neurol, 23 (4), 763-71
PubMed 26756429

Solberg M, Koht J (2016)
Dystonia induced by drug treatment
Tidsskr Nor Laegeforen, 136 (20), 1730
PubMed 27830908

Syvertsen M, Hellum MK, Hansen G, Edland A, Nakken KO, Selmer KK, Koht J (2016)
Prevalence of juvenile myoclonic epilepsy in people <30 years of age-A population-based study in Norway
Epilepsia, 58 (1), 105-112
PubMed 27861775

Trouillard O, Koht J, Gerstner T, Moland S, Depienne C, Dusart I, Méneret A, Ruiz M, Dubacq C, Roze E (2016)
Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature
Tremor Other Hyperkinet Mov (N Y), 6, 424
PubMed 27830107

Publications 2015

Gerstner T, Moland S, Koht J (2015)
Congenital mirror movements of the hands
Tidsskr Nor Laegeforen, 135 (20), 1852
PubMed 26534812

Syvertsen M, Koht J, Nakken KO (2015)
Prevalence and incidence of epilepsy in the Nordic countries
Tidsskr Nor Laegeforen, 135 (18), 1641-5
PubMed 26442732

Syvertsen M, Nakken KO, Edland A, Hansen G, Hellum MK, Koht J (2015)
Prevalence and etiology of epilepsy in a Norwegian county-A population based study
Epilepsia, 56 (5), 699-706
PubMed 25810072

Tesson C, Koht J, Stevanin G (2015)
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology
Hum Genet, 134 (6), 511-38
PubMed 25758904

Publications 2014

Koht J, Rengmark A, Opladen T, Bjørnarå KA, Selberg T, Tallaksen CM, Blau N, Toft M (2014)
Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene
Acta Neurol Scand Suppl (198), 7-12
PubMed 24588500

Wedding IM, Koht J, Tran GT, Misceo D, Selmer KK, Holmgren A, Frengen E, Bindoff L, Tallaksen CM, Tzoulis C (2014)
Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions
PLoS One, 9 (1), e86340
PubMed 24466038

Publications 2013

Wedding IM, Koht J, Dietrichs E, Landrø NI, Tallaksen CM (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 Neurol, 13, 186
PubMed 24289098

Publications 2012

Gras D, Jonard L, Roze E, Chantot-Bastaraud S, Koht J, Motte J, Rodriguez D, Louha M, Caubel I, Kemlin I, Lion-François L, Goizet C, Guillot L, Moutard ML, Epaud R, Héron B, Charles P, Tallot M, Camuzat A, Durr A, Polak M, Devos D, Sanlaville D, Vuillaume I, Billette de Villemeur T et al. (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
J Neurol Neurosurg Psychiatry, 83 (10), 956-62
PubMed 22832740

Publications 2011

Koht J, Stevanin G, Durr A, Mundwiller E, Brice A, Tallaksen CM (2011)
SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene
Acta Neurol Scand, 125 (2), 116-22
PubMed 21434874

Publications 2009

Anheim M, Monga B, Fleury M, Charles P, Barbot C, Salih M, Delaunoy JP, Fritsch M, Arning L, Synofzik M, Schöls L, Sequeiros J, Goizet C, Marelli C, Le Ber I, Koht J, Gazulla J, De Bleecker J, Mukhtar M, Drouot N, Ali-Pacha L, Benhassine T, Chbicheb M, M'Zahem A, Hamri A et al. (2009)
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
Brain, 132 (Pt 10), 2688-98
PubMed 19696032

Erichsen AK, Koht J, Stray-Pedersen A, Abdelnoor M, Tallaksen CM (2009)
Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study
Brain, 132 (Pt 6), 1577-88
PubMed 19339254

Koht J, Bjørnarå KA, Jørum E, Tallaksen CM (2009)
Ataxia with vitamin E deficiency in southeast Norway, case report
Acta Neurol Scand Suppl (189), 42-5
PubMed 19566498

Publications 2007

Koht J, Tallaksen CM (2007)
Cerebellar ataxia in the eastern and southern parts of Norway
Acta Neurol Scand Suppl, 187, 76-9
PubMed 17419835

Nakken KO, Brodtkorb E, Koht J (2007)
[Epilepsy and rehabilitation]
Tidsskr Nor Laegeforen, 127 (3), 309-12
PubMed 17279111

Publications 2006

Solberg DK, Koht J, Refsum H (2006)
[A 74-year-old unconscious woman with myoclonia and seizures]
Tidsskr Nor Laegeforen, 126 (17), 2275-6
PubMed 16977723

Publications 2005

Koht J, Braathen GJ, Neubert D, Russell MB (2005)
[Cerebral cavernous malformations]
Tidsskr Nor Laegeforen, 125 (15), 2008-10
PubMed 16100539