Zobrazeno 1 - 10
of 39
pro vyhledávání: '"F M Giardiello"'
Publikováno v:
Diagnostic Histopathology. 17:69-79
Polyps of the small bowel are rare compared to those of the colorectum. A correct histopathological diagnosis is crucial for the choice of subsequent treatment. This article reviews the most frequently found and some rare but distinct polyps and poly
Autor:
J. D. Trimbath, F. M. Giardiello
Publikováno v:
Alimentary Pharmacology & Therapeutics. 16:1843-1857
Summary Colorectal cancer is the second leading cause of cancer death, after lung cancer, in the USA. The great majority (80%) of patients with colorectal cancer have sporadic disease with no evidence of having inherited the disorder. In the remainin
Autor:
F. M. Giardiello
Publikováno v:
JAMA: The Journal of the American Medical Association. 278:1278-1281
Publikováno v:
Inflammatory bowel diseases. 2(1)
Patients with ulcerative colitis are at increased risk for colorectal adenocarcinoma compared with the general population. Although surveillance for colorectal malignancy and dysplasia (a premalignant lesion) has been recommended, a benefit in reduci
Autor:
F M Giardiello, Folkert H.M. Morsink, Lodewijk A.A. Brosens, W. A. Van Hattem, Ralph Carvalho, S Lens, G J A Offerhaus, W W J de Leng
Publikováno v:
Gut, 57(5), 623-627. BMJ Publishing Group
Background/aims: Juvenile polyposis syndrome (JPS) is a rare autosomal dominant disorder characterised by multiple gastrointestinal juvenile polyps and an increased risk of colorectal cancer. This syndrome is caused by germline mutation of either SMA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d70028924da302d07056d8297b7385e
https://pure.amc.nl/en/publications/large-genomic-deletions-of-smad4-bmpr1a-and-pten-in-juvenile-polyposis(d9e63290-d6bc-477a-a5fd-e438be51001c).html
https://pure.amc.nl/en/publications/large-genomic-deletions-of-smad4-bmpr1a-and-pten-in-juvenile-polyposis(d9e63290-d6bc-477a-a5fd-e438be51001c).html
Publikováno v:
Gut, 54(7), 1034-1043. BMJ Publishing Group
Familial adenomatous polyposis (FAP) is one of two well described forms of hereditary colorectal cancer. The primary cause of death from this syndrome is colorectal cancer which inevitably develops usually by the fifth decade of life. Screening by ge
Autor:
T M Bayless, F M Giardiello
Publikováno v:
Radiology. 199:28-30
Publikováno v:
Familial cancer. 1(3-4)
Autor:
M G, Sayed, A F, Ahmed, J R, Ringold, M E, Anderson, J L, Bair, F A, Mitros, H T, Lynch, S T, Tinley, G M, Petersen, F M, Giardiello, B, Vogelstein, J R, Howe
Publikováno v:
Annals of surgical oncology. 9(9)
Juvenile polyposis (JP) is an inherited condition predisposing to upper gastrointestinal (UGI) polyps and colorectal cancer. Two genes are known to predispose to JP, SMAD4 and bone morphogenetic protein receptor type 1A (BMPR1A). The object of this s
Autor:
J D, Trimbath, F M, Giardiello
Publikováno v:
Alimentary pharmacologytherapeutics. 16(11)
Colorectal cancer is the second leading cause of cancer death, after lung cancer, in the USA. The great majority (80%) of patients with colorectal cancer have sporadic disease with no evidence of having inherited the disorder. In the remaining 20%, a