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Virchows Archiv : an International Journal of Pathology|August 15, 2025
Cemento-osseous dysplasia with a NOTCH4 mutation: a case reportGerben E Breimer, Nard G Janssen, Anne M L Jansen, et al.
Virchows Archiv : an International Journal of Pathology|April 14, 2021
Genome-wide copy number variations as molecular diagnostic tool for cutaneous intermediate melanocytic lesions: a systematic review and individual patient data meta-analysisChiel F Ebbelaar, Anne M L Jansen, Lourens T Bloem, et al.
Familial Cancer|September 27, 2019
Novel candidates in early-onset familial colorectal cancerAnne M L Jansen, Pradipta Ghosh, Tikam C Dakal, et al.
British Journal of Cancer|January 6, 2026
Targeting the DNA damage response prevents regrowth of colorectal peritoneal metastasis-derived organoids following treatment with mitomycin CKyah van Megesen, Arianna Stefan, Madelief Kieboom, et al.
Virchows Archiv : an International Journal of Pathology|October 11, 2020
Expanding spectrum of "spitzoid" lesions: a small series of 4 cases with MAP2K1 mutationsK G P Kerckhoffs, T Aallali, C A Ambarus, et al.
The American Journal of Dermatopathology|June 25, 2025
A Stranger in the Slide: A Rare Collision of a Spitz Melanocytoma With a Novel MYH9::LTK Fusion and a Common BRAF Mutated Nevus Mimicking a Melanoma With a Preexistent NevusPuk R Meijs-Hermanns, Juliette M J Spitzer-Naaijkens, Lennart A Kester, et al.
Virchows Archiv : an International Journal of Pathology|June 18, 2021
Mind your head: two cases of mucosal metastasis of BRAF-mutated melanoma of the scalpS A Koppes, A M R Schrader, A M L Jansen, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|July 6, 2010
Variation in treatment and outcome in patients with non-small cell lung cancer by region, hospital type and volume in the NetherlandsM W J M Wouters, S Siesling, M L Jansen-Landheer, et al.
Molecular Genetics & Genomic Medicine|August 7, 2015
Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analysesHeleen M van der Klift, Anne M L Jansen, Niki van der Steenstraten, et al.
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