about
Pulmonary neuroendocrine (carcinoid) tumors: European Neuroendocrine Tumor Society expert consensus and recommendations for best practice for typical and atypical pulmonary carcinoidsSecretory apparatus assessed by analysis of pancreatic secretory stress protein expression in a rat model of chronic pancreatitisATG5 is induced by DNA-damaging agents and promotes mitotic catastrophe independent of autophagySporadic versus hereditary gastrinomas of the duodenum and pancreas: distinct clinico-pathological and epidemiological features.VHL-gene deletion in single renal tubular epithelial cells and renal tubular cysts: further evidence for a cyst-dependent progression pathway of clear cell renal carcinoma in von Hippel-Lindau disease.MicroRNA profile of poorly differentiated thyroid carcinomas: new diagnostic and prognostic insights.Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas.Consensus guidelines for the management of patients with liver metastases from digestive (neuro)endocrine tumors: foregut, midgut, hindgut, and unknown primary.Multicentre validation study of nucleic acids extraction from FFPE tissues.Pheochromocytoma in rats with multiple endocrine neoplasia (MENX) shares gene expression patterns with human pheochromocytoma.Neuroendocrine gastro-entero-pancreatic tumors: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.Sclerosing angiomatoid nodular transformation of the spleen presenting as a rapidly growing tumour in a patient with rectal cancerDeletions of 11q22.3-q25 are associated with atypical lung carcinoids and poor clinical outcome.Accumulation of FOXP3+T-cells in the tumor microenvironment is associated with an epithelial-mesenchymal-transition-type tumor budding phenotype and is an independent prognostic factor in surgically resected pancreatic ductal adenocarcinomaA novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas.Mutation and expression analyses reveal differential subcellular compartmentalization of PTEN in endocrine pancreatic tumors compared to normal islet cellsA selective COX-2 inhibitor suppresses chronic pancreatitis in an animal model (WBN/Kob rats): significant reduction of macrophage infiltration and fibrosisMolecular genetics of gastroenteropancreatic endocrine tumors.TNM staging of foregut (neuro)endocrine tumors: a consensus proposal including a grading system.Allelic deletion of the MEN1 gene in duodenal gastrin and somatostatin cell neoplasms and their precursor lesions.New Genetics and Genomic Data on Pancreatic Neuroendocrine Tumors: Implications for Diagnosis, Treatment, and Targeted Therapies.PTEN alterations of the stromal cells characterise an aggressive subpopulation of pancreatic cancer with enhanced metastatic potential.Exocrine meets endocrine: pancreatic stone protein and regenerating protein--two sides of the same coin.An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.Gastrinoma (duodenal and pancreatic).TNM staging of midgut and hindgut (neuro) endocrine tumors: a consensus proposal including a grading system.Site-specific biology and pathology of gastroenteropancreatic neuroendocrine tumors.Molecular profiles of gastroenteropancreatic endocrine tumors.Islet inflammation in type 2 diabetes: from metabolic stress to therapy.p73 regulates autophagy and hepatocellular lipid metabolism through a transcriptional activation of the ATG5 gene.Successful Medical Treatment of Adult Nesidioblastosis With Pasireotide over 3 Years: A Case Report.Comprehensive MicroRNA expression profiling identifies novel markers in follicular variant of papillary thyroid carcinoma.ENETS Consensus Guidelines for the Standards of Care in Neuroendocrine Tumors: towards a standardized approach to the diagnosis of gastroenteropancreatic neuroendocrine tumors and their prognostic stratification.Loss of Raf-1 kinase inhibitor protein (RKIP) is strongly associated with high-grade tumor budding and correlates with an aggressive phenotype in pancreatic ductal adenocarcinoma (PDAC)ENETS consensus guidelines for the management of brain, cardiac and ovarian metastases from neuroendocrine tumors.Clinical aspects, diagnostic challenges and management of patients with neuroendocrine tumors (NETs).ENETS Consensus Guidelines for the management of patients with neuroendocrine neoplasms from the jejuno-ileum and the appendix including goblet cell carcinomas.Tall cell papillary thyroid carcinoma: new diagnostic criteria and mutations in BRAF and TERT.Pathology: Classification and Immunoprofile.Autophagy inhibition improves sunitinib efficacy in pancreatic neuroendocrine tumors via a lysosome-dependent mechanism.
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hulumtues
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Aurel Perren
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Aurel Perren
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Aurel Perren
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Aurel Perren
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Aurel Perren
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Aurel Perren
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Aurel Perren
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Aurel Perren
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P214
P1053
A-9383-2018
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7004126842
P21
P214
P31
P496
0000-0002-6819-6092
P734
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viaf-305639187