Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Arthur S. Aelvoet"'
Autor:
Arthur S. Aelvoet, Isabel Martin, James Cockburn, Cherryl Cabalit, Victoria Cuthill, Duncan Spalding, Olivier Busch, Barbara A.J. Bastiaansen, Susan K. Clark, Evelien Dekker, Andrew Latchford
Publikováno v:
Endoscopy International Open, Vol 12, Iss 05, Pp E659-E665 (2024)
Externí odkaz:
https://doaj.org/article/2a82ecdc01c54d669bb7a3ce9b1566e3
Autor:
Arthur S. Aelvoet, John G. Karstensen, Barbara A.J. Bastiaansen, Monique E. van Leerdam, Francesc Balaguer, Michal Kaminski, Roel Hompes, Patrick M.M. Bossuyt, Luigi Ricciardiello, Andrew Latchford, Rodrigo Jover, Maria Daca-Alvarez, Maria Pellisé, Evelien Dekker, European FAP Consortium
Publikováno v:
Endoscopy International Open, Vol 11, Iss 11, Pp E1056-E1062 (2023)
Externí odkaz:
https://doaj.org/article/700c2049202e4fe1951c87c136738c7c
Autor:
Jasmijn D. G. Linssen, Sanne M. van Neerven, Arthur S. Aelvoet, Clara C. Elbers, Louis Vermeulen, Evelien Dekker
Publikováno v:
BMC Gastroenterology, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Familial adenomatous polyposis (FAP) is a rare autosomal dominant disease characterized by germline mutations in the Adenomatous Polyposis Coli (APC) gene, resulting in the development of numerous colorectal adenomas. As these pat
Externí odkaz:
https://doaj.org/article/ffade250e9774a58b2a30de9ed0884a7
Autor:
Arthur S. Aelvoet, Maria Pellisé, Barbara A.J. Bastiaansen, Monique E. van Leerdam, Rodrigo Jover, Francesc Balaguer, Michal F. Kaminski, John G. Karstensen, Jean-Christophe Saurin, Roel Hompes, Patrick M.M. Bossuyt, Luigi Ricciardiello, Andrew Latchford, Evelien Dekker
Publikováno v:
Endoscopy International Open, Vol 11, Iss 04, Pp E386-E393 (2023)
Background and study aims Patients with familial adenomatous polyposis (FAP) undergo colectomy and lifelong endoscopic surveillance to prevent colorectal, duodenal and gastric cancer. Endoscopy has advanced significantly in recent years, including bo
Externí odkaz:
https://doaj.org/article/8032b9c9dbc84757a12af376de85c136
Autor:
Arthur S. Aelvoet, Barbara A.J. Bastiaansen, Paul Fockens, Marc G. Besselink, Olivier R. Busch, Evelien Dekker
Publikováno v:
HPB, 24(10), 1642-1650. John Wiley and Sons Inc.
Background: In patients with familial adenomatous polyposis (FAP), extensive nonmalignant duodenal polyposis not amenable to endoscopic management demands surgical resection for which pancreas-preserving total duodenectomy (PPTD) offers a pancreatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732816e4484dd4ba8241bf1d6a898241
https://doi.org/10.1016/j.hpb.2022.04.004
https://doi.org/10.1016/j.hpb.2022.04.004
Autor:
Arthur S. Aelvoet, Daniël R. Hoekman, Bert J. W. Redeker, Jitske Weegenaar, Evelien Dekker, Carel J. M. van Noesel, Floor A. M. Duijkers
Publikováno v:
Familial cancer, 22(1), 49-54. Springer Netherlands
Biallelic MSH3 germline variants are a rare cause of adenomatous polyposis as yet reported in two small families only. We describe the phenotype of a third family, the largest thus far, with adenomatous polyposis related to compound heterozygous MSH3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6126b2592befc062ebb856b24f497379
https://doi.org/10.1007/s10689-022-00297-x
https://doi.org/10.1007/s10689-022-00297-x
Publikováno v:
Best practice & research. Clinical gastroenterology.
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis syndromes with a high colorectal cancer (CRC) risk. Therefore, frequent endoscopic surveillance including polypectomy of relevant premalignant lesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc32e0b895fdff6ae18b98a9e782f03d
https://doi.org/10.1016/j.bpg.2022.101793
https://doi.org/10.1016/j.bpg.2022.101793
Autor:
Evelien Dekker, Victorine H. Roos, Barbara A. J. Bastiaansen, Paul Fockens, Patrick M.M. Bossuyt, Arthur S. Aelvoet, Frank G. J. Kallenberg
Publikováno v:
Gastrointestinal endoscopy, 93(2), 457-466. Mosby Inc.
Background and Aims Almost all patients with familial adenomatous polyposis (FAP) develop duodenal adenomas, with a 4% to 18% risk of progression into duodenal cancer. Prophylactic endoscopic resection of duodenal adenomas may prevent cancer and is c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9286107555af206e2870abaef590a3f8
https://doi.org/10.1016/j.gie.2020.05.065
https://doi.org/10.1016/j.gie.2020.05.065
Autor:
Arthur S. Aelvoet, Victorine H. Roos, Barbara A.J. Bastiaansen, Roel Hompes, Willem A. Bemelman, Cora M. Aalfs, Patrick M.M. Bossuyt, Evelien Dekker
Publikováno v:
Gastrointestinal endoscopy, 97(1), 69-77.e1. Mosby Inc.
Background and Aims: Patients with familial adenomatous polyposis (FAP) undergo (procto)colectomy to prevent colorectal cancer from developing. Interestingly, after proctocolectomy with ileal pouch-anal anastomosis (IPAA), most patients develop adeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c224e1e0b51a344636165b1507980ecb
http://www.scopus.com/inward/record.url?scp=85141815645&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85141815645&partnerID=8YFLogxK
Autor:
Arthur S. Aelvoet, Daphne Struik, Barbara A. J. Bastiaansen, Willem A. Bemelman, Roel Hompes, Patrick M. M. Bossuyt, Evelien Dekker
Publikováno v:
Familial cancer. 21(4)
Abstract Desmoid tumours (DT) are one of the main causes of death in patients with familial adenomatous polyposis (FAP). Surgical trauma is a risk factor for DT, yet a colectomy is inevitable in FAP to prevent colorectal cancer. This systematic revie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5ce3938499ea6a08574e118c773cc30
https://pubmed.ncbi.nlm.nih.gov/35022961
https://pubmed.ncbi.nlm.nih.gov/35022961