multiple endocrine neoplasia type 2


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multiple endocrine neoplasia type 2

(1) MEN 2A (multiple endocrine neoplasia type 2A).
(2) Multiple endocrine neoplasia type 2B (type 3).
References in periodicals archive ?
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
Very early detection of RET protooncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children: presence of C-cell malignant disease in asymptomatic carriers.
Pheochromocytoma in von Hippel-Lindau disease: distinct histopathologic phenotype compared to pheochromocytoma in multiple endocrine neoplasia type 2.
RET oligonucleotide microarray for the detection of RET mutations in multiple endocrine neoplasia type 2 syndromes.
Denaturing gradient gel electrophoresis to diagnose multiple endocrine neoplasia type 2.
Granular-cell pituicytoma associated with multiple endocrine neoplasia type 2.
Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis.
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2.
Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma.

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