about
P3373
Prevalence and incidence of epilepsy in the Nordic countriesBenign hereditary chorea, not only chorea: a family case presentationDelving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosologySpastic paraplegia type 7 is associated with multiple mitochondrial DNA deletionsCongenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the LiteraturePrevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity.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.Targeted high throughput sequencing in hereditary ataxia and spastic paraplegiaPrevalence and etiology of epilepsy in a Norwegian county-A population based study.Prevalence of juvenile myoclonic epilepsy in people <30 years of age-A population-based study in Norway.Oculogyric Crises.Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.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.Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.Cerebellar ataxia in the eastern and southern parts of Norway.Ataxia with vitamin E deficiency in southeast Norway, case report.SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.A founder mutation p.H701P identified as a major cause of SPG7 in Norway.Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene.[Epilepsy and rehabilitation][A 74-year-old unconscious woman with myoclonia and seizures]Congenital mirror movements of the handsHomocarnosinosis: A historical update and findings in the SPG11 gene
P50
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P50
description
Noors onderzoekster
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hulumtuese
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norsk nevrolog
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researcher
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հետազոտող
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name
Jeanette Koht
@ast
Jeanette Koht
@en
Jeanette Koht
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Jeanette Koht
@nb
Jeanette Koht
@nl
Jeanette Koht
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Jeanette Koht
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type
label
Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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altLabel
Jeanette Aimee Koht
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prefLabel
Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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Jeanette Koht
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P214
P106
P2038
Jeanette_Koht
P21
P214
P2287
P27
P31
P3373
P496
0000-0002-5499-0818