Tl-201 chloride scan in multiple endocrine neoplasia type 2A.

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Diagnosis and surgical treatment of multiple endocrine neoplasia type 2A.

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Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A.

Local recurrence of pheochromocytoma in multiple endocrine neoplasia type 2A: a diagnostic and therapeutic challenge.

Nonfunctional Metastatic Parathyroid Carcinoma in the Setting of Multiple Endocrine Neoplasia Type 2A Syndrome.

My, How Things Have Changed in Multiple Endocrine Neoplasia Type 2A!

Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families.

Prominent corneal nerves in patients with multiple endocrine neoplasia type 2A: diagnostic implications.

Incidence of prominent corneal nerves in multiple endocrine neoplasia type 2A.

RET Cys634Arg mutation confers a more aggressive multiple endocrine neoplasia type 2A phenotype than Cys634Tyr mutation.

The association between Hirschsprung's disease and multiple endocrine neoplasia type 2a: a systematic review.

Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.

Gastroenteropancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1.

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Laryngeal neuroma in multiple endocrine neoplasia type 2B.

[Life saving glance diagnosis in type IIb multiple endocrine neoplasia].

Recurrent hyperparathyroidism due to proliferation of autotransplanted parathyroid tissue in a multiple endocrine neoplasia type 2A patient.

Vaginal delivery in a patient with pheochromocytoma, medullary thyroid cancer, and primary hyperparathyroidism (multiple endocrine neoplasia type 2A, Sipple's syndrome).

The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10.

Missed Diagnosis of Multiple Endocrine Neoplasia Type 2 B.

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Local recurrence of pheochromocytoma in multiple endocrine neoplasia type 2A: a diagnostic and therapeutic challenge.

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