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How traumatic is breast cancer? Post-traumatic stress symptoms (PTSS) and risk factors for severe PTSS at 3 and 15 months after surgery in a nationwide cohort of Danish women treated for primary breast cancer.
- Published in:
- 2011
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- Publication type:
- journal article
Reply.
- Published in:
- 2016
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- Publication type:
- Letter
Circulating Elastin Fragments Are Not Affected by Hepatic, Renal and Hemodynamic Changes, But Reflect Survival in Cirrhosis with TIPS.
- Published in:
- 2015
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- Publication type:
- journal article
Peroperative concentrations of cefuroxime in serum and subcutaneous tissue following antimicrobial prophylaxis in gastrointestinal surgery.
- Published in:
- 1988
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- Publication type:
- Letter
Breast cancer with different prognostic characteristics developing in Danish women using hormone replacement therapy.
- Published in:
- 2004
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- Publication type:
- journal article
Quantifying dose perturbations in high‐risk prostate radiotherapy due to translational and rotational motion of prostate and pelvic lymph nodes.
- Published in:
- Medical Physics, 2024, v. 51, n. 11, p. 8423, doi. 10.1002/mp.17366
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- Publication type:
- Article
Spectral Theory of Massless Pauli-Fierz Models.
- Published in:
- Communications in Mathematical Physics, 2004, v. 249, n. 1, p. 29, doi. 10.1007/s00220-004-1111-x
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- Publication type:
- Article
Energy layer optimization strategies for intensity‐modulated proton therapy of lung cancer patients.
- Published in:
- Medical Physics, 2018, v. 45, n. 10, p. 4355, doi. 10.1002/mp.13139
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- Publication type:
- Article
PRRT2 benign familial infantile seizures (BFIS) with atypical evolution to encephalopathy related to status epilepticus during sleep (ESES).
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- Neurological Sciences, 2023, v. 44, n. 6, p. 2173, doi. 10.1007/s10072-023-06735-7
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- Publication type:
- Article
Sex-specific disease modifiers in juvenile myoclonic epilepsy.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-06324-2
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- Publication type:
- Article
Deep-Phenotyping the Less Severe Spectrum of PIGT Deficiency and Linking the Gene to Myoclonic Atonic Seizures.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.663643
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- Publication type:
- Article
The responsible citizen: An investigation of the Theatre of the Oppressed.
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- Applied Theatre Research, 2018, v. 6, n. 2, p. 139, doi. 10.1386/atr.6.2.139_1
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- Publication type:
- Article
Two cytosolic glutamine synthetase isoforms play specific roles for seed germination and seed yield structure in Arabidopsis.
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- Journal of Experimental Botany, 2015, v. 66, n. 1, p. 203, doi. 10.1093/jxb/eru411
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- Publication type:
- Article
Two cytosolic glutamine synthetase isoforms play specific roles for seed germination and seed yield structure in Arabidopsis.
- Published in:
- Journal of Experimental Botany, 2014, v. 65, n. 18, p. 203, doi. 10.1093/jxb/eru411
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- Publication type:
- Article
Mowat–Wilson syndrome: an underdiagnosed syndrome?
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- Clinical Genetics, 2008, v. 73, n. 6, p. 579, doi. 10.1111/j.1399-0004.2008.00997.x
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- Publication type:
- Article
Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobe.
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- Clinical Genetics, 2007, v. 72, n. 6, p. 593, doi. 10.1111/j.1399-0004.2007.00901.x
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- Publication type:
- Article
NIPA1 mutation in complex hereditary spastic paraplegia with epilepsy.
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- European Journal of Neurology, 2011, v. 18, n. 9, p. 1197, doi. 10.1111/j.1468-1331.2011.03359.x
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- Publication type:
- Article
Atypical Vitamin B6 Deficiency: A Rare Cause of Unexplained Neonatal and Infantile Epilepsies.
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- Journal of Child Neurology, 2014, v. 29, n. 5, p. 704, doi. 10.1177/0883073813505354
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- Publication type:
- Article
Prematurity in Greenland. A study of infants with a birthweight below 2000 g.
- Published in:
- 1996
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- Publication type:
- journal article
Continuous Intravenous Infusion of Ampicillin and Gentamicin during Parenteral Nutrition to 36 Newborn Infants Using a Dosage Schedule.
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- Acta Paediatrica, 1984, v. 73, n. 2, p. 203, doi. 10.1111/j.1651-2227.1984.tb09929.x
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- Publication type:
- Article
Correlations of receptor desensitization of gain-of-function GABRB3 variants with clinical severity.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 1, p. 224, doi. 10.1093/brain/awad285
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- Publication type:
- Article
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 9, p. 3885, doi. 10.1093/brain/awad111
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- Publication type:
- Article
Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 3, p. 923, doi. 10.1093/brain/awac305
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- Publication type:
- Article
Reply: Genotype-phenotype correlations in SCN8A-related epilepsy: a cohort study of Chinese children in southern China.
- Published in:
- 2022
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- Publication type:
- Editorial
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
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- 2021
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- Publication type:
- journal article
A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants.
- Published in:
- 2020
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- Publication type:
- journal article
The first step towards personalized risk prediction for common epilepsies.
- Published in:
- 2019
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- Publication type:
- journal article
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability.
- Published in:
- 2019
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- Publication type:
- journal article
Migraine with aura and risk of silent brain infarcts and white matter hyperintensities: an MRI study.
- Published in:
- 2016
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- Publication type:
- journal article
CHD2 variants are a risk factor for photosensitivity in epilepsy.
- Published in:
- Brain: A Journal of Neurology, 2015, v. 138, n. 5, p. 1198, doi. 10.1093/brain/awv052
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- Publication type:
- Article
Mutations in KCNT1 cause a spectrum of focal epilepsies.
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- Epilepsia (Series 4), 2015, v. 56, n. 9, p. e114, doi. 10.1111/epi.13071
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- Publication type:
- Article
The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: A population-based study from 2004 to 2009.
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- Epilepsia (Series 4), 2015, v. 56, n. 4, p. e36, doi. 10.1111/epi.12927
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- Publication type:
- Article
Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-Convergence on axonal guidance.
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- Epilepsia (Series 4), 2014, v. 55, n. 12, p. 2017, doi. 10.1111/epi.12839
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- Publication type:
- Article
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers.
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- Epilepsia (Series 4), 2013, v. 54, n. 5, p. e74, doi. 10.1111/epi.12124
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- Publication type:
- Article
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy.
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- Epilepsia (Series 4), 2013, v. 54, n. 2, p. 265, doi. 10.1111/epi.12084
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- Publication type:
- Article
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.
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- Epilepsia (Series 4), 2013, v. 54, n. 2, p. 256, doi. 10.1111/epi.12078
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- Publication type:
- Article
A balanced translocation disrupts SYNGAP1 in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA).
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- Epilepsia (Series 4), 2011, v. 52, n. 12, p. e190, doi. 10.1111/j.1528-1167.2011.03304.x
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- Publication type:
- Article
Balanced translocation in a patient with severe myoclonic epilepsy of infancy disrupts the sodium channel gene SCN1A.
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- Epilepsia (Series 4), 2008, v. 49, n. 6, p. 1091, doi. 10.1111/j.1528-1167.2008.01550.x
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- Publication type:
- Article
Functional Effects of Epilepsy Associated KCNT1 Mutations Suggest Pathogenesis via Aberrant Inhibitory Neuronal Activity.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 23, p. 15133, doi. 10.3390/ijms232315133
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- Publication type:
- Article
Refining Genotypes and Phenotypes in KCNA2 -Related Neurological Disorders.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 6, p. 2824, doi. 10.3390/ijms22062824
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- Publication type:
- Article
Microbial formation of nitrite-cured pigment, nitrosylmyoglobin, from metmyoglobin in model systems and smoked fermented sausages by Lactobacillus fermentum strains and a commercial starter culture.
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- European Food Research & Technology, 2003, v. 216, n. 6, p. 463
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- Publication type:
- Article
The angular position of a refuge affects escape responses in staghorn sculpin Leptocottus armatus.
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- Journal of Fish Biology, 2017, v. 90, n. 6, p. 2434, doi. 10.1111/jfb.13306
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- Publication type:
- Article
A standardized patient-centered characterization of the phenotypic spectrum of PCDH19 girls clustering epilepsy.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0803-0
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- Publication type:
- Article
PRO‐C3 and ADAPT algorithm accurately identify patients with advanced fibrosis due to alcohol‐related liver disease.
- Published in:
- Alimentary Pharmacology & Therapeutics, 2021, v. 54, n. 5, p. 699, doi. 10.1111/apt.16513
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- Publication type:
- Article
Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29280-x
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- Publication type:
- Article
Tamoxifen for one year versus two years versus 6 months of Tamoxifen and 6 months of megestrol acetate: a randomized comparison in postmenopausal patients with high-risk breast cancer (DBCG 89C)
- Published in:
- 2008
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- Publication type:
- Journal Article
Validity and representativity in the Danish Breast Cancer Cooperative Group: a study on protocol allocation and data validity from one county to a multi-centre database.
- Published in:
- 2003
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- Publication type:
- Journal Article
Erratum: Sequence analysis of 17 NRXN1 deletions.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 3, p. 261, doi. 10.1002/ajmg.b.32226
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- Publication type:
- Article
Sequence analysis of 17 NRXN1 deletions.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 52, doi. 10.1002/ajmg.b.32204
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- Publication type:
- Article
Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 3, p. 354, doi. 10.1002/ajmg.b.32036
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- Publication type:
- Article