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1 sociated with germline RET mutations causing multiple endocrine neoplasia type 2.
2 of oncogenic Ret receptor in a fly model of Multiple Endocrine Neoplasia Type 2.
3 or cure the endocrinopathies associated with multiple endocrine neoplasia type 2.
4 among patients with Hirschsprung disease and multiple endocrine neoplasia type 2.
5 evelopment of the inherited cancer syndrome, multiple endocrine neoplasia type 2.
6 ch encodes a receptor tyrosine kinase, cause multiple endocrine neoplasia type 2.
7 agement of phaeochromocytoma associated with multiple endocrine neoplasia type 2.
8 ly active oncogenic RET, were found to cause multiple endocrine neoplasia type 2, a dominant inherite
9 sing a Ret-kinase-driven Drosophila model of multiple endocrine neoplasia type 2 and kinome-wide drug
10 n-based study compiled data on patients with multiple endocrine neoplasia type 2 from 30 academic med
11 ast year addressing the surgical approach to multiple endocrine neoplasia type 2 in the pediatric pop
12 phaeochromocytoma (MIM No 171300) occurs in multiple endocrine neoplasia type 2 (MEN 2) (MIM No 1714
16 sible for the familial tumor syndrome called multiple endocrine neoplasia type 2 (MEN 2) that include
17 ase underlies the genesis and progression of multiple endocrine neoplasia type 2 (MEN 2), a dominantl
18 ery cell of the body) mutations in RET cause multiple endocrine neoplasia type 2 (MEN 2), an inherite
19 ibility are von Hippel-Lindau disease (VHL), multiple endocrine neoplasia type 2 (MEN 2), the newly d
22 s patients with von Hippel-Lindau disease or multiple endocrine neoplasia type 2 (MEN-2), is hindered
24 and nonmedullary thyroid cancers related to multiple endocrine neoplasia type 2 (MEN2), Cowden syndr
29 r, the other major neoplasia associated with multiple endocrine neoplasia type 2, phaeochromocytoma,
32 of medullary thyroid cancer in patients with multiple endocrine neoplasia type 2 syndrome has demonst
34 tential therapeutic agents for patients with multiple endocrine neoplasia type 2 tumors because both,
36 somal dominantly inherited cancer syndromes, multiple endocrine neoplasia type 2, von Hippel-Lindau d
37 d for 84% of the patients; the other 16% had multiple endocrine neoplasia type 2, von Recklinghausen'
39 gical intervention in children affected with multiple endocrine neoplasia type 2 will lead to better
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