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Bilateral pheochromocytoma and islet cell adenoma of the pancreas

Known as: Islet cell tumor syndrome, Familial pheochromocytoma, Familial islet cell tumors 
National Institutes of Health

Papers overview

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2017
2017
Summary Pheochromocytomas (PCCs) and paragangliomas (PGLs) are rare tumours with a heterogeneous genetic background. Up to 40% of… 
Review
2011
Review
2011
Although a large kindred with familial pheochromocytoma (Pheo) and paraganglioma (PGL) was discovered in 1962 and later found to… 
Highly Cited
1995
Highly Cited
1995
Pheochromocytomas occur sporadically and are associated with several dominantly inherited cancer syndromes, including von Hippel… 
1993
1993
CgA is a 49 kilodalton peptide produced by a variety of endocrine and neuroendocrine tissues and secreted with tissue-specific… 
1988
1988
A family was investigated with an increased occurrence of pheochromocytoma. Three males out of 7 family members showed… 
1982
1982
SummaryA case of bilateral aniridia associated with familial pheochromocytoma in a female of 17 years of age was described. The… 
Review
1963
Review
1963
M ULTIPLE neurofibromatosis occurs in 5-~5 per cent of patients with phcochromocytomas. I,~,4 The first recorded case of… 
1961
1961