Pia Pinholt Munksgaard

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Pia Pinholt Munksgaard

  • Institut for Folkesundhed - Almen Medicin
Postaddresse:
Bartholins Allé 2
1260, 1.27
8000
Aarhus C
Danmark

E-mail: ppm@ph.au.dk

Mobil: +4521913717

Telefon: +4587167924

Publikationer

En omkostningsanalyse af den indledende fase af "Tjek dit helbred" i Randers Kommune

Rasmussen, S. R., Klausen Fredslund, E., Munksgaard, P. P., Sandbæk, A. & Maindal, H. T., jul. 2014, 34 s.

TOX3 (TNRC9) overexpression in bladder cancer cells decreases cellular proliferation and triggers an interferon-like response

Birkenkamp-Demtröder, K., Mansilla, F., Andersen, L. D., Thorsen, K., Fristrup, N., Brems-Eskildsen, A. S., Madsen, P. P., Sørensen, K. D., Borre, M. & Ørntoft, T. F., jan. 2013, I : Journal of Molecular Biomarkers & Diagnosis. 4, 1, s. 1-11 11 s.

High Expression of Karyopherin-α2 Defines Poor Prognosis in Non-Muscle-Invasive Bladder Cancer and in Patients with Invasive Bladder Cancer Undergoing Radical Cystectomy

Jensen, J. B., Munksgaard, P. P., Sørensen, C. M., Fristrup, N., Birkenkamp-Demtroder, K., Ulhøi, B. P., Jensen, K. M-E., Orntoft, T. F. & Andersen, L. D., maj 2011, I : European Urology Supplements. 59, 5, s. 841-848 8 s.

Prediction and diagnosis of bladder cancer recurrence based on urinary content of hTERT, SENP1, PPP1CA, and MCM5 transcripts

Brems-Eskildsen, A. S., Zieger, K. E. A., Toldbod, H., Holcomb, C., Higuchi, R., Mansilla, F., Munksgaard, P. P., Borre, M., Ørntoft, T. F. & Andersen, L. D., 2010, I : B M C Cancer. 10, 1, s. 646

Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping.

Madsen, P. P., 1 dec. 2006, I : Human Genetics. 118, 6, s. 680-90 11 s.

TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping

Maydan, G., Andresen, B. S., Madsen, P. P., Zeigler, M., Raas-Rothschild, A., Zlotogorski, A., Gutman, A. & Korman, S. H., 17 aug. 2006, I : Journal of Inherited Metabolic Disease. 29, 5, s. 620-6 6 s.

  How exonic point mutations can affect splicing and cause disease - Examples on disruption of exonic splicing regulatory elements in the human acyl-Coa dehydrogenasegenes

Nielsen, K. B., Madsen, P. P., Schrøder, L. D., Gregersen, N. & Andresen, B. S., 2004.