5 results match your criteria: "Dr. Hancken Clinic[Affiliation]"
Ear Nose Throat J
June 2022
Department of Otorhinolaryngology Head and Neck Surgery, Elbe Klinikum Stade, Stade, Germany.
Leiomyosarcoma (LMS) in the sinonasal tract (SNT) is a rarity that has been firstly described in 1958. Since then, there have been only a few articles about this entity. Most of the data available about LMS in the SNT is derived from case reports.
View Article and Find Full Text PDFRadiol Res Pract
August 2020
Diagnostic and Interventional Radiology, Dr. Hancken Clinic, 21680 Stade, Germany.
Today, there are still no uniform guidelines for the treatment of epistaxis. Furthermore, it is widely debated whether embolization or surgical approaches should be the first choice of treatment for intractable posterior epistaxis after conservative measures have failed. In several meta-analyses, it is reported that endoscopic sphenopalatine artery ligation and embolization have similar success rates, but embolization was associated with more severe neurological complications.
View Article and Find Full Text PDFCardiovasc Intervent Radiol
August 2020
53 N Studios UG (haftungsbeschraenkt), Diedrich-Speckmann-Weg 2, 21682, Stade, Germany.
Kidney Int
December 2017
Department of Radiology, University Hospital of Cologne, Kerpener Str. 62, 50937 Cologne, Germany. Electronic address:
Polycystic kidney disease (PKD) is among the leading causes of end-stage renal disease. Increasing evidence exists that molecular therapeutic strategies targeted to cyst formation and growth might be more efficacious in early disease stages, highlighting the growing need for sensitive biomarkers. Here we apply quantitative magnetic resonance imaging techniques of T2 mapping and diffusion-weighted imaging in the jck mouse model for PKD using a clinical 3.
View Article and Find Full Text PDFBMC Med Genet
May 2017
Department II of Internal Medicine and Center for Molecular Medicine Cologne, University of Cologne, Kerpener Str. 62, 50937, Cologne, Germany.
Background: Renal cell carcinoma is among the most prevalent malignancies. It is generally sporadic. However, genetic studies of rare familial forms have led to the identification of mutations in causative genes such as VHL and FLCN.
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