Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sabine Fransis"'
Autor:
Michaël Verquin, MD, DDS, Christophe Politis, MD, DDS, François Thonnart, MD, DDS, Sabine Fransis, MD, Serge Schepers, MD, DDS
Publikováno v:
JAAD Case Reports, Vol 21, Iss , Pp 59-62 (2022)
Externí odkaz:
https://doaj.org/article/b66858536cc74a688f40bc4ed25e9d86
Autor:
Jeroen Swinnen, MD, Geert Gelin, MD, Sabine Fransis, MD, Jan Vandevenne, MD, PhD, Sofie Van Cauter, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 14, Iss 11, Pp 1334-1347 (2019)
We present a rare case of an isocitrate dehydrogenase-wildtype glioblastoma with histologically proven parotid, cervical lymph node, and lung metastases. While recent therapy advances are likely to increase glioblastoma mid- and long-term survival, t
Externí odkaz:
https://doaj.org/article/3b6ed6c2985d41c3807fe7ce0c3f7167
Publikováno v:
Kidney International Reports, Vol 1, Iss 3, Pp 131-134 (2016)
Externí odkaz:
https://doaj.org/article/a7d11e2f81b8423c9b0971ffc2697936
Publikováno v:
Indian Journal of Surgical Oncology.
Urachal carcinoma (UC) is a rare and aggressive tumor arising from the urachal remnants, with the potential for peritoneal dissemination. Patients diagnosed with UC often have a poor prognosis. To date, there is no standardized treatment. Our objecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71330eb0f3a9813ac238c26be3099aef
https://doi.org/10.1007/s13193-022-01679-4
https://doi.org/10.1007/s13193-022-01679-4
Publikováno v:
Radiology Case Reports, Vol 14, Iss 11, Pp 1334-1347 (2019)
Radiology Case Reports
Radiology Case Reports
We present a rare case of an isocitrate dehydrogenase-wildtype glioblastoma with histologically proven parotid, cervical lymph node, and lung metastases. While recent therapy advances are likely to increase glioblastoma mid- and long-term survival, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e561ff64130f733424d15d915e4d1c80
https://doi.org/10.1016/j.radcr.2019.08.011
https://doi.org/10.1016/j.radcr.2019.08.011
Autor:
Patrick Schöffski, Luc Dehaspe, Isabelle Vanden Bempt, Bart Neuville, Maria Debiec-Rychter, Lien Spans, Stefan Lehnert, Sara Vander Borght, Hilde Brems, Raf Sciot, Eric Legius, Sofie Claerhout, Sabine Fransis, Baki Topal
Publikováno v:
Genes, chromosomescancerREFERENCES. 60(4)
Mutational analysis guides therapeutic decision making in patients with advanced-stage gastrointestinal stromal tumors (GISTs). We evaluated three targeted next-generation sequencing (NGS) assays, consecutively used over 4 years in our laboratory for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::356bf55ced50383a9415b6ad743dcbbf
https://pubmed.ncbi.nlm.nih.gov/33258138
https://pubmed.ncbi.nlm.nih.gov/33258138
Publikováno v:
Case Reports in Perinatal Medicine. 9
Objectives Agnathia-otocephaly complex (AOC) is an extremely rare, lethal disorder causing obstruction of the upper airway at birth due to absence of the mandible and hypoplasia of the oral cavity. Implications for future pregnancies need to be eluci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c660d0d9259150fc0a3a55829393ac9
https://doi.org/10.1515/crpm-2020-0041
https://doi.org/10.1515/crpm-2020-0041
Publikováno v:
Kidney International Reports
Kidney International Reports, Vol 1, Iss 3, Pp 131-134 (2016)
Kidney International Reports, Vol 1, Iss 3, Pp 131-134 (2016)
Heleen Ameye, Sabine Fransis, Evelyne Lerut, Christoph Metalidis and Ben Sprangers Department of Nephrology, University Hospitals Leuven, Leuven, Belgium; Department of Pathology, Ziekenhuis OostLimburg Hospital, Genk, Belgium; Department of Morpholo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28490fd497653f433be315c677a88e7a
http://europepmc.org/articles/PMC5678843
http://europepmc.org/articles/PMC5678843
Autor:
Pieter Evenepoel, Yves Vanrenterghem, Bart Maes, Kathleen Claes, Sabine Fransis, Dirk Kuypers, Siegfried Segaert, Miranda Zeegers, Patrick Flamen
Publikováno v:
Nephrology Dialysis Transplantation. 19:469-473
Nephrogenic fibrosing dermopathy (NFD) is a rare, recently described cutaneous fibrosing disorder that primarily affects patients with a history of renal disease [1]. Since the first report in 2000 by Cowper et al., about 100 cases of NFD have been d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb0f16e8952e250dca73d37b4c34f8e2
https://doi.org/10.1093/ndt/gfg506
https://doi.org/10.1093/ndt/gfg506
Autor:
Johan Auwerx, Jef Verbeek, Sabine Fransis, Eija Pirinen, Frederik Nevens, David Cassiman, Paul P. Van Veldhoven, Karin Thevissen, Chantal Ceuterick-de Groote, Matthias Lannoo, Ingrid Vander Elst, Bruno P. A. Cammue, Jos van Pelt, Pieter Spincemaille, Peter Van Eyken, Petra Windmolders, Dongryeol Ryu, Pierre Bedossa
Publikováno v:
Gut : the journal of the British Society for Gastroenterology
Objective No therapy for non-alcoholic steatohepatitis (NASH) has been approved so far. Roux-en-y gastric bypass (RYGB) is emerging as a therapeutic option, although its effect on NASH and related hepatic molecular pathways is unclear from human stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df11b9dfeb59fa8af2a3313b10db1846
https://pubmed.ncbi.nlm.nih.gov/25080449
https://pubmed.ncbi.nlm.nih.gov/25080449