Maria Rasmussen
6PUBLICATIONS
2CO-AUTHORS
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Publications (6)
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|Jan 09, 2025
MUC1-associated autosomal dominant tubulointerstitial kidney disease: prevalence in kidney failure of undetermined aetiology and clinical insights from Danish families.Jeff Granhøj, Dorte L Lildballe, Katja V Pedersen
|Jul 18, 2024
The role of genomic disorders in chronic kidney failure of undetermined aetiology ≤50 years.Jeff Granhøj, Katja Venborg Pedersen, Mads Malik Aagaard
|Nov 10, 2021
Functional megalin is expressed in renal cysts in a mouse model of adult polycystic kidney disease.Marlene L Nielsen, Mia C Mundt, Dorte L Lildballe
|Jul 05, 2021
Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion.Signe Faurschou, Dorte L Lildballe, Lisa L Maroun
|Feb 24, 2021
PAX2 variant associated with bilateral kidney agenesis and broad intrafamilial disease variability.Maria Rasmussen, Marlene Louise Nielsen, J Robert Manak
|Dec 02, 2017
Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies.M Rasmussen, L Sunde, M L Nielsen
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