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Journal Article
Cancer, ISSN 0008-543X, 10/2008, Volume 113, Issue S7, pp. 1807 - 1843
Pancreatic endocrine tumors (PETs) can occur as part of 4 inherited disorders, including Multiple Endocrine Neoplasia type 1 (MEN1), von Hippel‐Lindau disease... 
pancreatic endocrine tumors | Multiple Endocrine Neoplasia type 1 | von Hippel‐Lindau disease | insulinomas | Zollinger‐Ellison syndrome | tuberous sclerosis | neurofibromatosis 1 | neuroendocrine tumors | gastrinomas | Pancreatic endocrine tumors | Gastrinomas | Insulinomas | Zollinger-Ellison syndrome | Tuberous sclerosis | Multiple endocrine neoplasia type 1 | Neurofibromatosis 1 | Neuroendocrine tumors | Von Hippel-Lindau disease | SOMATOSTATIN-RECEPTOR SCINTIGRAPHY | NEOPLASIA-TYPE-I | von Hippel-Lindau disease | HIPPEL-LINDAU-DISEASE | GASTROENTEROPANCREATIC NEUROENDOCRINE TUMORS | ZOLLINGER-ELLISON-SYNDROME | GASTRIC-ACID HYPERSECRETION | POSITRON-EMISSION-TOMOGRAPHY | TUBEROUS SCLEROSIS COMPLEX | ONCOLOGY | ISLET-CELL TUMORS | VON-RECKLINGHAUSENS-DISEASE | von Hippel-Lindau Disease - therapy | Prognosis | Pancreatic Neoplasms - diagnosis | Humans | Multiple Endocrine Neoplasia Type 1 - diagnosis | Neurofibromatosis 1 - diagnosis | Pancreatic Neoplasms - genetics | von Hippel-Lindau Disease - genetics | Multiple Endocrine Neoplasia Type 1 - genetics | Neurofibromatosis 1 - therapy | Tuberous Sclerosis - genetics | Tuberous Sclerosis - therapy | von Hippel-Lindau Disease - diagnosis | Multiple Endocrine Neoplasia Type 1 - therapy | Tuberous Sclerosis - diagnosis | Neurofibromatosis 1 - genetics | Pancreatic Neoplasms - therapy | Development and progression | Pancreatic tumors | Genetic aspects | multiple endocrine neoplasia type 1
Journal Article