The relationship of molecular genetic to clinical diagnosis of familial hypercholesterolemia in a Danish population
Damgaard, Dorte, Larsen, Mogens L., Nissen, Peter H., Jensen, Jesper M., Jensen, Henrik K., Soerensen, Vibeke R., Jensen, Lillian G., Faergeman, Ole
Published in Atherosclerosis (01.05.2005)
Published in Atherosclerosis (01.05.2005)
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Journal Article
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation
HAUBEK, DORTE, GJØRUP, HANS, JENSEN, LILLIAN G., JUNCKER, INGER, NYEGAARD, METTE, BØRGLUM, ANDERS D., POULSEN, SVEN, HERTZ, JENS M.
Published in International journal of paediatric dentistry (01.11.2011)
Published in International journal of paediatric dentistry (01.11.2011)
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Journal Article
Making the Case for Criticality: A Novel Approach to Nursing Product Education
Jensen, Lillian, Dobbs, Julie, Updike, Alisha
Published in The Journal of nursing administration (01.01.2024)
Published in The Journal of nursing administration (01.01.2024)
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Journal Article
COASTing Through Bedside Report: An Innovative Approach to Safe Transitions of Care
Webster, Kristi, Hlebichuk, Jeanne, Jensen, Lillian, Zastrow, Rachel
Published in Journal of nursing care quality (15.08.2024)
Published in Journal of nursing care quality (15.08.2024)
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Journal Article
Hackathons: Practical Problem-Solving for Nurse Educators
Bigott, Veronica, Jensen, Lillian, Zidek, Stephanie
Published in The American journal of nursing (01.07.2023)
Published in The American journal of nursing (01.07.2023)
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Journal Article
Two mutations in the same low-density lipoprotein receptor allele act in synergy to reduce receptor function in heterozygous familial hypercholesterolemia
Jensen, Henrik K., Jensen, Thomas G., Faergeman, Ole, Jensen, Lillian G., Andresen, Brage S., Corydon, Morten J., Andreasen, Per H., Hansen, Peter S., Heath, Finn, Bolund, Lars, Gregersen, Niels
Published in Human mutation (1997)
Published in Human mutation (1997)
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Journal Article
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation: FAM83H-associated hypocalcified AI
HAUBEK, DORTE, GJØRUP, HANS, JENSEN, LILLIAN G., JUNCKER, INGER, NYEGAARD, METTE, BØRGLUM, ANDERS D., POULSEN, SVEN, HERTZ, JENS M.
Published in International journal of paediatric dentistry (01.11.2011)
Published in International journal of paediatric dentistry (01.11.2011)
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Journal Article
No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes
Damgaard, Dorte, Jensen, Jesper Moeller, Larsen, Mogens Lytken, Soerensen, Vibeke Reiche, Jensen, Henrik Kjaerulf, Gregersen, Niels, Jensen, Lillian Gryesten, Faergeman, Ole
Published in Atherosclerosis (01.12.2004)
Published in Atherosclerosis (01.12.2004)
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Journal Article
Obesity: prevention and treatment. The Danish Society of Obesity Research
Kroustrup, Jens Peter, Sørensen, Thorkild I A, Jensen, Lillian
Published in Ugeskrift for læger (20.03.2006)
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Published in Ugeskrift for læger (20.03.2006)
Journal Article
Improved RNase protection assay for quantifying LDL-receptor mRNA ; estimation of analytical imprecision and biological variance in peripheral blood mononuclear cells
PETERSEN, N. E, LARSEN, L. K, NISSEN, H, JENSEN, L. G, JENSEN, A, PETERSEN, P. H, HORDER, M, GREGERSEN, N, KRISTIANSEN, K
Published in Clinical chemistry (Baltimore, Md.) (01.11.1995)
Published in Clinical chemistry (Baltimore, Md.) (01.11.1995)
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