Found: 18
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Cytokine Patterns as Predictors of Antibiotic Treatment Effect in Chronic Low Back Pain with Modic Changes: Subgroup Analyses of a Randomized Trial (AIM Study).
- Published in:
- Journal of Pain Research, 2023, v. 16, p. 1713, doi. 10.2147/JPR.S406079
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- Publication type:
- Article
Pathogenic variants in KCTD7 perturb neuronal K<sup>+</sup> fluxes and glutamine transport.
- Published in:
- Brain: A Journal of Neurology, 2016, v. 139, n. 12, p. 3109, doi. 10.1093/brain/aww244
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- Article
Inherited retinal disease in Norway – a characterization of current clinical and genetic knowledge.
- Published in:
- Acta Ophthalmologica (1755375X), 2020, v. 98, n. 3, p. 286, doi. 10.1111/aos.14218
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- Publication type:
- Article
Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene.
- Published in:
- Acta Ophthalmologica (1755375X), 2010, v. 88, n. 3, p. 323, doi. 10.1111/j.1755-3768.2008.01465.x
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- Article
Spastic Paraplegia Type 7 Is Associated with Multiple Mitochondrial DNA Deletions.
- Published in:
- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0086340
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- Publication type:
- Article
Friedreich ataxia in Norway - an epidemiological, molecular and clinical study.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0328-4
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- Publication type:
- Article
Friedreich ataxia in Norway -- an epidemiological, molecular and clinical study.
- Published in:
- Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0328-4
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- Publication type:
- Article
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
- Published in:
- Human Mutation, 2016, v. 37, n. 7, p. 711, doi. 10.1002/humu.22997
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- Publication type:
- Article
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
- Published in:
- Human Mutation, 2016, v. 37, n. 4, p. 359, doi. 10.1002/humu.22960
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- Publication type:
- Article
Decreased serum concentrations of antiseizure medications in children with drug resistant epilepsy following treatment with ketogenic diet.
- Published in:
- Epilepsia Open, 2023, v. 8, n. 3, p. 858, doi. 10.1002/epi4.12746
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- Publication type:
- Article
novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 21, p. 1919, doi. 10.1093/hmg/ddab144
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- Publication type:
- Article
Health‐related quality of life in adults with drug‐resistant focal epilepsy treated with modified Atkins diet in a randomized clinical trial.
- Published in:
- Epilepsia (Series 4), 2023, v. 64, n. 5, p. e69, doi. 10.1111/epi.17585
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- Publication type:
- Article
Genome‐wide decrease in DNA methylation in adults with epilepsy treated with modified ketogenic diet: A prospective study.
- Published in:
- Epilepsia (Series 4), 2022, v. 63, n. 9, p. 2413, doi. 10.1111/epi.17351
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- Publication type:
- Article
Substantial early changes in bone and calcium metabolism among adult pharmacoresistant epilepsy patients on a modified Atkins diet.
- Published in:
- Epilepsia (Series 4), 2022, v. 63, n. 4, p. 880, doi. 10.1111/epi.17169
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- Publication type:
- Article
Prevalence of juvenile myoclonic epilepsy in people <30 years of age-A population-based study in Norway.
- Published in:
- Epilepsia (Series 4), 2017, v. 58, n. 1, p. 105, doi. 10.1111/epi.13613
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- Publication type:
- Article
The effect of infliximab in patients with chronic low back pain and Modic changes (the BackToBasic study): study protocol of a randomized, double blind, placebo-controlled, multicenter trial.
- Published in:
- 2020
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- Publication type:
- journal article
Pyruvatdehydrogenase-mangel.
- Published in:
- Journal of the Norwegian Medical Association / Tidsskrift for Den Norske Laegeforening, 2019, p. 1473, doi. 10.4045/tidsskr.18.0988
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- Publication type:
- Article
Pyruvatdehydrogenase-mangel.
- Published in:
- Journal of the Norwegian Medical Association / Tidsskrift for Den Norske Laegeforening, 2019, v. 139, n. 15, p. 1473
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- Publication type:
- Article