Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
about
Endocrine neoplasms in familial syndromes of hyperparathyroidismMultiple endocrine neoplasia type 2: achievements and current challengesGerman Association of Endocrine Surgeons practice guideline for the surgical management of malignant thyroid tumors.Germline RET sequence variation I852M and occult medullary thyroid cancer: harmless polymorphism or causative mutation?Familial prevalence and age of RET germline mutations: implications for screening.Risk-oriented approach to hereditary adrenal pheochromocytoma.The characterization of pheochromocytoma and its impact on overall survival in multiple endocrine neoplasia type 2Paragangliomas/Pheochromocytomas: clinically oriented genetic testingPersonalized medicine: the future is not what it used to be.Simultaneous bilateral laparoscopic adrenalectomy for pheochromocytoma in multiple endocrine neoplasia (MEN) syndrome: Case report with review literaturePheochromocytoma as the first manifestation of MEN2A with RET mutation S891A: report of a case.Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.Diagnosis, treatment, and follow-up of medullary thyroid carcinoma: recommendations by the Thyroid Department of the Brazilian Society of Endocrinology and Metabolism.Genotype-phenotype correlation in multiple endocrine neoplasia type 2Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes.Pheochromocytoma in an 8-year-old patient with multiple endocrine neoplasia type 2A: implications for screening.Translational research in endocrine surgery.Biologic and Clinical Perspectives on Thyroid Cancer.Phaeochromocytoma in multiple endocrine neoplasia type 2: RET codon-specific penetrance and changes in management during the last four decades.Bilateral Pheochromocytomas in MEN2A Syndrome: A Two-Institution Experience.A large Chinese pedigree of multiple endocrine neoplasia type 2A with a novel C634Y/D707E germline mutation in RET exon 11Bilateral adrenal pheochromocytoma with a germline L790F mutation in the RET oncogene.Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.Extent of surgery for phaeochromocytomas in the genomic era.Mutation screening in a Norwegian cohort with pheochromocytoma.Diversity of mutations in the RET proto-oncogene and its oncogenic mechanism in medullary thyroid cancer.Asymptomatic bilateral adrenal pheochromocytoma in a patient with a germline V804M mutation in the RET proto-oncogene.Early diagnosis of multiple endocrine neoplasia type 2B: a challenge for physicians.A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?
P2860
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P2860
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
description
2005 nî lūn-bûn
@nan
2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
@ast
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
@en
type
label
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
@ast
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
@en
prefLabel
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
@ast
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
@en
P2093
P356
P1476
Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2.
@en
P2093
Andreas Machens
Hendrik Lehnert
Michael Brauckhoff
Phuong Nguyen Thanh
P304
P356
10.1210/JC.2005-0064
P407
P577
2005-04-12T00:00:00Z