VIICTR
Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
GAGEL, ROBERT F
One or more keywords matched the following items that are connected to
GAGEL, ROBERT F
Item Type
Name
Academic Article
The clinical outcome of prospective screening for multiple endocrine neoplasia type 2a. An 18-year experience.
Academic Article
Natural history of familial medullary thyroid carcinoma: effect of a program for early diagnosis.
Academic Article
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.
Academic Article
Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma.
Academic Article
Adrenal medullary hyperplasia. A morphometric analysis in patients with familial medullary thyroid carcinoma.
Academic Article
Pheochromocytoma, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
Academic Article
Multiple endocrine neoplasia type II and familial medullary thyroid carcinoma. Impact of genetic screening on management.
Academic Article
Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomas.
Academic Article
Pheochromocytoma and medullary thyroid carcinoma: a new genotype-phenotype correlation of the RET protooncogene 891 germline mutation.
Academic Article
The evolving field of tyrosine kinase inhibitors in the treatment of endocrine tumors.
Academic Article
Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?
Academic Article
Multiple endocrine neoplasia type 2a associated with cutaneous lichen amyloidosis.
Academic Article
Impact of prospective screening for multiple endocrine neoplasia type 2.
Academic Article
Natural history of the familial medullary thyroid carcinoma-pheochromocytoma syndrome and the identification of preneoplastic stages by screening studies: a five-year report.
Academic Article
Screening for MEN1 mutations in patients with atypical endocrine neoplasia.
Academic Article
The role of genetics in the surgical management of familial endocrinopathy syndromes.
Academic Article
Surgical management of hereditary pheochromocytoma.
Academic Article
Changing concepts in the management of hereditary and sporadic medullary thyroid carcinoma.
Academic Article
The clinical and screening age-at-onset distribution for the MEN-2 syndrome.
Concept
Pheochromocytoma
Academic Article
The characterization of pheochromocytoma and its impact on overall survival in multiple endocrine neoplasia type 2.
Academic Article
Natural history of familial medullary carcinoma of the thyroid gland (MCT) pheochromocytoma syndrome and the identification of preneoplastic stages by screening tests. A five year report
Academic Article
Surgical management of hereditary pheochromocytoma
Academic Article
Recontacting Patients with Updated Genetic Testing Recommendations for Medullary Thyroid Carcinoma and Pheochromocytoma or Paraganglioma.
Search Criteria
Pheochromocytoma