Results 131 to 140 of about 287,756 (345)
Journal of Hepato-Biliary-Pancreatic Sciences, EarlyView.ABSTRACT Background Although pancreaticobiliary maljunction (PBM) is associated with a high incidence of biliary cancer, it often goes undiagnosed. This means that the true prevalence of PBM and the incidence of biliary cancer are unknown. High confluence of the pancreaticobiliary ducts (HCPBD) may be an intermediate PBM variant, though reports are ...
Shintaro Shirai +6 more
wiley +1 more source
JPGN Reports, EarlyView.Abstract Constitutional mismatch repair deficiency (CMMRD) is a rare hereditary cancer syndrome resulting from biallelic mutations in DNA mismatch repair (MMR) genes that lead to early‐onset cancers in children, including lymphoma and colorectal cancer (CRC).
Chloe J. Cohan +3 more
wiley +1 more source
Telangiectatic adenoma: a variant of hepatocellular adenoma
Annals of Hepatology, 2004 Figure: benign, well-limited hepatocellular tumor with major haemorrhagic foci and telangiectasia on histology. Beside Focal Nodular Hyperplasia and hepatocellular adenomas, the most frequent benign hepatocellular lesion in the liver, a variant, initially called «telangiectatic focal nodular hyperplasia» now claimed as “telangiectatic adenoma” has been
openaire +4 more sources
Temporal‐Parotid Resection for Malignant Parotid Tumors: A Systematic Review
The Laryngoscope, EarlyView.Parotid gland tumors represent a complex surgical challenge. Temporal‐parotid resection (TPR) is indicated to manage temporal bone invasion. Thirteen studies investigated the role of TPR in literature, including 336 patients. High rates of negative margins and local disease control are achieved with TPR.
Antonio Daloiso +7 more
wiley +1 more source
Mass spectrometry imaging of N‐linked glycans: Fundamentals and recent advances
Mass Spectrometry Reviews, EarlyView.Abstract With implications in several medical conditions, N‐linked glycosylation is one of the most important posttranslation modifications present in all living organisms. Due to their nontemplate synthesis, glycan structures are extraordinarily complex and require multiple analytical techniques for complete structural elucidation.
Tana V. Palomino, David C. Muddiman
wiley +1 more source
Thyroid Adenomas in Sheep administered Iodine-131 Daily [PDF]
, 1957 L.K. Bustad +3 more
openalex +1 more source
Med Research, EarlyView.ABSTRACT Familial adenomatous polyposis (FAP) is a well‐characterized hereditary colorectal cancer syndrome driven by germline mutations in the APC gene. KRAS mutations, although more common in sporadic colorectal and endometrial cancers, are rarely seen concurrently in patients with FAP.
Tongchuan Yin +4 more
wiley +1 more source