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Multiple Endocrine Neoplasia Type 1

Known as: Multiple Endocrine Neoplasia, Type I, Multiple Endocrine Neoplasia Type 1 [Disease/Finding], MEA Type 1 
A form of multiple endocrine neoplasia that is characterized by the combined occurrence of tumors in the PARATHYROID GLANDS, the PITUITARY GLAND, and… 
National Institutes of Health

Papers overview

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Review
2008
Review
2008
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the occurrence of tumors of the… 
Highly Cited
2007
Highly Cited
2007
CONTEXT Germline mutations in the MEN1 gene predispose to multiple endocrine neoplasia type 1 (MEN1) syndrome, but in up to 20-25… 
Highly Cited
2005
Highly Cited
2005
Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal‐dominant syndrome associated with neoplasia of pituitary, pancreas… 
Highly Cited
2003
Highly Cited
2003
Little is known of the natural history of thymic carcinoids in multiple endocrine neoplasia type 1 (MEN1). This is important… 
Review
1998
Review
1998
Endocrine Neoplasias in Relation to Oncogenes and Tumor Suppressor Genes Dr. Allen M. Spiegel (Metabolic Diseases Branch… 
Highly Cited
1997
Highly Cited
1997
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids… 
Highly Cited
1997
Highly Cited
1997
Familial multiple endocrine neoplasia type 1 (FMEN1) is an autosomal dominant trait characterized by tumors of the parathyroids… 
Highly Cited
1996
Highly Cited
1996
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the combined occurrence of… 
Highly Cited
1989
Highly Cited
1989
Familial multiple endocrine neoplasia type 1 (MEN-1) is characterized by tumors of the parathyroids, endocrine pancreas, and…