Search Results - "Hasholt, Lis"

Upregulated Chaperone-Mediated Autophagy May Perform a Key Role in Reduced Cancer Incidence in Huntington's Disease.

Authors: Hasholt, Lis Frydenreich¹ (AUTHOR) hasholt@sund.ku.dk

Source: Journal of Huntington's Disease. 2023, Vol. 12 Issue 4, p371-376. 6p.

The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease.

Authors: Hasholt, Lis Ballegaard, Martin Bundgaard, Henning et al.

Source: Scandinavian Journal of Clinical & Laboratory Investigation. Dec2017, Vol. 77 Issue 8, p617-621. 5p.

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Localization of A11-reactive oligomeric species in prion diseases.

Authors: Aidt, Frederik H Hasholt, Lis F Christiansen, Michael et al.

Source: Histopathology. Jul2013, Vol. 62 Issue 7, p994-1001. 8p. 3 Color Photographs, 2 Charts.

Platelet serotonin transporters and the transporter gene in control subjects, unipolar patients and bipolar patients.

Authors: Mellerup, Erling Bennike, Bente Bolwig, Tom et al.

Source: Acta Psychiatrica Scandinavica. Mar2001, Vol. 103 Issue 3, p229-233. 5p. 2 Charts.

Subjects: Serotonin, Genetic polymorphisms

Seasonal difference in brain serotonin transporter binding predicts symptom severity in patients with seasonal affective disorder.

Authors: Mahon, Brenda Mc Andersen, Sofie B. Madsen, Martin K. et al.

Source: Brain: A Journal of Neurology; 5/1/2016, Vol. 139 Issue 5, p1605-1614, 10p

Attitudes of Persons at Risk for Fabry's Disease Towards Predictive Tests and Genetic Counselling.

Authors: Sørensen, S. A. Hasholt, Lis

Source: Journal of Biosocial Science. Jan1983, Vol. 15 Issue 1, p89-94. 6p.

Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience.

Authors: Effraimidis, Grigoris Rasmussen, Åse Krogh Dunoe, Morten et al.

Source: PLoS ONE. 11/16/2022, Vol. 17 Issue 11, p1-18. 18p.

Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women.

Authors: Havndrup, Ole Christiansen, Michael Stoevring, Birgitte et al.

Source: European Journal of Heart Failure. Jun2010, Vol. 12 Issue 6, p535-540. 6p. 1 Diagram, 1 Chart, 1 Graph.

Autonomic skin responses in females with Fabry disease.

Authors: Møller, Anette T. Bach, Flemming W. Feldt-Rasmussen, Ulla et al.

Source: Journal of the Peripheral Nervous System. Sep2009, Vol. 14 Issue 3, p159-164. 6p. 1 Chart, 1 Graph.

Small-fibre neuropathy in female Fabry patients: reduced allodynia and skin blood flow after topical capsaicin.

Authors: Moller, Anette T. Feldt-Rasmussen, Ulla Rasmussen, Åse K. et al.

Source: Journal of the Peripheral Nervous System. Jun2006, Vol. 11 Issue 2, p119-125. 7p. 6 Graphs.

Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience.

Authors: Effraimidis, Grigoris Rasmussen, Åse Krogh Dunoe, Morten et al.

Source: PLoS ONE. 6/8/2023, Vol. 18 Issue 6, p1-1. 1p.

Paroxysmal Cranial Dyskinesia and Nail‐Patella Syndrome Caused by a Novel Variant in the LMX1B Gene.

Authors: Bech, Sara Løkkegaard, Annemette Nielsen, Troels T. et al.

Source: Movement Disorders. Dec2020, Vol. 35 Issue 12, p2343-2347. 5p.

Analysis of FMR1 (CGG)n alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia.

Authors: Larsen, Lars Allan Armstrong, Judith SM Grønskov, Karen et al.

Source: European Journal of Human Genetics. Oct99, Vol. 7 Issue 7, p771. 7p.

Cascade screening outcome in a nationwide cohort and genotype-phenotype relationship.

Authors: Effraimidis, Grigorios Rasmussen, Åse Krogh Hasholt, Lis Frydenreich et al.

Source: Molecular Genetics & Metabolism. Feb2020, Vol. 129 Issue 2, pS52-S52. 1p.

Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease model.

Authors: Reynolds, Regina Hertfelder Petersen, Maria Hvidberg Willert, Cecilie Wennemoes et al.

Source: MCN: Molecular & Cellular Neuroscience. Apr2018, Vol. 88, p118-129. 12p.

Liver function in Huntington's disease assessed by blood biochemical analyses in a clinical setting.

Authors: Nielsen, Signe Marie Borch Vinther-Jensen, Tua Nielsen, Jørgen E. et al.

Source: Journal of the Neurological Sciences. Mar2016, Vol. 362, p326-332. 7p.

Ghrelin‐mediated improvements in the metabolic phenotype in the R6/2 mouse model of Huntington's disease.

Authors: Rudenko, Olga Springer, Cecilie Skov, Louisa J. et al.

Source: Journal of Neuroendocrinology. Jul2019, Vol. 31 Issue 7, pN.PAG-N.PAG. 1p.

Three-Week Bright-Light Intervention Has Dose-Related Effects on Threat-Related Corticolimbic Reactivity and Functional Coupling.

Authors: Fisher, Patrick M. Madsen, Martin K. McMahon, Brenda et al.

Source: Biological Psychiatry. Aug2014, Vol. 76 Issue 4, p332-339. 8p.

Diagnostic dilemma: A young woman with Fabry disease symptoms, no family history, and a “sequencing cryptic” α-galactosidase a large deletion

Authors: Feldt-Rasmussen, Ulla Dobrovolny, Robert Nazarenko, Irina et al.

Source: Molecular Genetics & Metabolism. Nov2011, Vol. 104 Issue 3, p314-318. 5p.