Multiple endocrine neoplasia Type 2

Multiple endocrine neoplasia caused by mutation of the RET gene. It includes the following neoplastic processes: multiple endocrine neoplasia type 2A… (More)
National Institutes of Health

Papers overview

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Review
2012
Review
2012
Multiple endocrine neoplasia type 2 is an autosomal-dominant hereditary cancer syndrome caused by missense gain-of-function… (More)
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Review
2010
Review
2010
Multiple endocrine neoplasia type 2 (MEN2) is a autosomal dominat inherited tumour-syndrome caused by germline activating… (More)
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Review
2006
Review
2006
Multiple Endocrine Neoplasia Type 2 (MEN2) is a rare hereditary complex disorder characterized by the presence of medullary… (More)
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Highly Cited
2005
Highly Cited
2005
CONTEXT Recent data suggest a codon-specific, age-related development of multiple endocrine neoplasia type 2. OBJECTIVE The… (More)
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Highly Cited
2001
Highly Cited
2001
This study examined the mechanisms linking different biochemical and clinical phenotypes of pheochromocytoma in multiple… (More)
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Highly Cited
1999
Highly Cited
1999
BACKGROUND The detection of pheochromocytomas in patients at risk for these tumors, such as patients with von Hippel-Lindau… (More)
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1998
1998
In a few patients with Hirschsprung disease (HSCR) and no clinical symptoms of multiple endocrine neoplasia type 2 (MEN-2A) or… (More)
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Highly Cited
1995
Highly Cited
1995
The International RET Mutation Consortium was first convened as part of the Fifth International Workshop on Multiple Endocrine… (More)
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Highly Cited
1994
Highly Cited
1994
MULTIPLE endocrine neoplasia type 2 (MEN 2) comprises three clinically distinct, dominantly inherited cancer syndromes. MEN 2A… (More)
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Highly Cited
1993
Highly Cited
1993
BACKGROUND Pheochromocytoma is a feature of two disorders with an autosomal dominant pattern of inheritance--multiple endocrine… (More)
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