Works matching Multiple endocrine neoplasia type 2 (MEN 2)
Results: 88
Ganglioneuromatous polyposis associated with type 2 B multiple endocrine neoplasia (MEN 2B) - case report.
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- Annals of Agricultural & Environmental Medicine, 2024, v. 31, n. 2, p. 302, doi. 10.26444/aaem/171736
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- Article
The Gene Causing Multiple Endocrine Neoplasia Type 2 (MEN 2).
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- Annals of Medicine, 1994, v. 26, n. 3, p. 199, doi. 10.3109/07853899409147890
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- Article
Multiple endocrine neoplasia type 2 syndromes (MEN 2): results from the ItaMEN network analysis on the prevalence of different genotypes and phenotypes.
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- European Journal of Endocrinology, 2010, v. 163, n. 2, p. 301, doi. 10.1530/EJE-10-0333
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- Article
DNA Testing for More Sophisticated Clinical Management of Multiple Endocrine Neoplasia Type 2 (Men 2).
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- Japanese Journal of Clinical Oncology, 1998, v. 28, n. 10, p. 588, doi. 10.1093/jjco/28.10.588
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- Article
Evaluation of potential mechanisms underlying genotype–phenotype correlations in multiple endocrine neoplasia type 2.
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- Oncogene, 2006, v. 25, n. 50, p. 6637, doi. 10.1038/sj.onc.1209669
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- Article
Elevated Calcitonin Levels in a Patient With a Pheochromocytoma: A Case Report.
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- American Surgeon, 2023, v. 89, n. 12, p. 6227, doi. 10.1177/00031348221117035
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- Article
Transcription Association of VHL and SDH Mutations Link Hypoxia and Oxidoreductase Signals in Pheochromocytomas.
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- Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 208, doi. 10.1196/annals.1353.023
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- Article
Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children: presence of C-cell malignant disease in asymptomatic carriers.
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- 2002
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- journal article
Prophylactic thyroidectomy in multiple endocrine neoplasia type 2.
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- Expert Review of Endocrinology & Metabolism, 2010, v. 5, n. 6, p. 867, doi. 10.1586/EEM.10.58
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- Article
Multiple endocrine neoplasia type 2.
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- Expert Review of Endocrinology & Metabolism, 2009, v. 4, n. 5, p. 443, doi. 10.1586/EEM.09.33
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- Article
Thyroid Malignancy and Cutaneous Lichen Amyloidosis: Key Points Amid RET Pathogenic Variants in Medullary Thyroid Cancer/Multiple Endocrine Neoplasia Type 2 (MEN2).
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- International Journal of Molecular Sciences, 2024, v. 25, n. 18, p. 9765, doi. 10.3390/ijms25189765
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- Article
The minisequencing method: a simple strategy for genetic screening of MEN 2 families.
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- BMC Genetics, 2002, v. 3, p. 8, doi. 10.1186/1471-2156-3-8
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- Article
Analysis of Mutations of the RET Proto-oncogene in Patients with Medullary Thyroid Carcinoma.
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- Russian Journal of Genetics, 2003, v. 39, n. 6, p. 706, doi. 10.1023/A:1024474314212
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- Article
Prophylactic thyroidectomy in multiple endocrine neoplasia: the impact of molecular mechanisms of RET proto-oncogene.
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- Langenbeck's Archives of Surgery, 2003, v. 388, n. 1, p. 17, doi. 10.1007/s00423-003-0368-4
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- Article
No correlation between RET immunostaining and the codon 918 mutation in sporadic medullary thyroid carcinoma.
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- Langenbeck's Archives of Surgery, 1999, v. 384, n. 1, p. 60, doi. 10.1007/s004230050175
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- Article
Laparoscopic bilateral cortical-sparing adrenalectomy for pheochromocytoma.
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- 2016
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- journal article
The mouse soluble GFRα4 receptor activates RET independently of its ligand persephin.
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- Oncogene, 2007, v. 26, n. 26, p. 3892, doi. 10.1038/sj.onc.1210161
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- Article
A model for GFRa4 function and a potential modifying role in multiple endocrine neoplasia 2.
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- Oncogene, 2005, v. 24, n. 6, p. 1091, doi. 10.1038/sj.onc.1207826
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- Article
The pressure rises: update on the genetics of phaeochromocytoma.
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- Human Molecular Genetics, 2002, v. 11, n. 20, p. 2347, doi. 10.1093/hmg/11.20.2347
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- Article
Genetic Predisposition to Phaeochromocytoma: Analysis of Candidate Genes GDNF, RET and VHL.
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- Human Molecular Genetics, 1997, v. 6, n. 7, p. 1051, doi. 10.1093/hmg/6.7.1051
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- Article
Haplotype analysis of MEN 2 mutations.
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- Human Molecular Genetics, 1994, v. 3, n. 10, p. 1771
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- Article
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.
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- Human Molecular Genetics, 1994, v. 3, n. 2, p. 237
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- Article
Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease.
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- 2001
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- journal article
Survival at 20 Years of a Medullary Thyroid Carcinoma with Bone and Pulmonary Metastases.
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- Pan Arab Journal of Oncology, 2016, v. 9, n. 2, p. 30
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- Article
Poster Presentations on Adrenal, Pituitary, and Other Endocrine Glands, Parathyroid Gland, Thyroid Gland.
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- 2016
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- Case Study
High prevalence of exon 8 G533 C mutation in apparently sporadic medullary thyroid carcinoma in Greece.
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- Clinical Endocrinology, 2012, v. 77, n. 6, p. 857, doi. 10.1111/j.1365-2265.2012.04462.x
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- Article
Phaeochromocytoma, new genes and screening strategies.
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- 2006
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- Other
RET codon 804 mutations in multiple endocrine neoplasia 2: genotype-phenotype correlations and implications in clinical management.
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- Clinical Genetics, 2011, v. 79, n. 1, p. 1, doi. 10.1111/j.1399-0004.2010.01453.x
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- Article
RET is expressed but not mutated in extra-adrenal paragangliomas.
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- Journal of Pathology, 2000, v. 191, n. 3, p. 264, doi. 10.1002/1096-9896(2000)9999:9999<::AID-PATH638>3.0.CO;2-I
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- Article
Anesthetic Management of Clinically Silent Familial Pheochromocytoma with MEN 2A: A Report of Four Cases.
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- Indian Journal of Surgery, 2016, v. 78, n. 5, p. 414, doi. 10.1007/s12262-016-1539-1
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- Article
Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET.
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- 2008
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- journal article
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and...
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- Nature, 1994, v. 367, n. 6461, p. 375, doi. 10.1038/367375a0
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- Article
Dermal Hyperneury and Multiple Sclerotic Fibromas in Multiple Endocrine Neoplasia Type 2A Syndrome.
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- 2017
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- journal article
Genotype—Phenotype Correlation of Patients with Multiple Endocrine Neoplasia Type 2 in Japan.
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- Japanese Journal of Clinical Oncology, 1998, v. 28, n. 10, p. 590, doi. 10.1093/jjco/28.10.590
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- Article
A Nationwide Clinical Survey of Patients With Multiple Endocrine Neoplasia Type 2 and Familial Medullary Thyroid Carcinoma in Japan.
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- Japanese Journal of Clinical Oncology, 1997, v. 27, n. 3, p. 128
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- Article
Germ Line Mutation in the RET Proto-oncogene Associated with Familial Multiple Endocrine Neoplasia Type 2B: A Case Report.
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- Japanese Journal of Clinical Oncology, 1995, v. 25, n. 3, p. 104
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- Article
Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.
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- European Journal of Human Genetics, 2002, v. 10, n. 8, p. 457, doi. 10.1038/sj.ejhg.5200829
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- Article
Genetic diagnosis of endocrine disorders in Cyprus through the Cyprus Institute of Neurology and Genetics: an ENDO-ERN Reference Center.
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- Orphanet Journal of Rare Diseases, 2024, v. 19, p. 1, doi. 10.1186/s13023-024-03171-4
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- Article
Medullary thyroid carcinoma identified within the first year of life in children with hereditary multiple endocrine neoplasia type 2A (codon 634) and 2B.
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- European Journal of Endocrinology, 2009, v. 160, n. 5, p. 807, doi. 10.1530/EJE-08-0854
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- Article
Different expression of catecholamine transporters in phaeochromocytomas from patients with von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2.
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- European Journal of Endocrinology, 2005, v. 153, n. 4, p. 551, doi. 10.1530/eje.1.01987
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- Article
Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma.
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- Oncogene, 2002, v. 21, n. 3, p. 479, doi. 10.1038/sj.onc.1205133
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- Article
Allelic imbalance of the mutant and wild-type RET allele in MEN 2A-associated medullary thyroid carcinoma.
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- Oncogene, 2001, v. 20, n. 53, p. 7809, doi. 10.1038/sj.onc.1204991
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- Article
Medullary Thyroid Carcinoma in a Patient with MEN 1 Syndrome. Case Report and Literature Review.
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- OncoTargets & Therapy, 2020, v. 13, p. 7599, doi. 10.2147/OTT.S259656
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- Article
CR56 Metastatic thyroid cancer after thyroidectomy in patient with MEN2A syndrome: a case report.
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- Lijecnicki Vjesnik, 2023, v. 145, p. 74, doi. 10.26800/LV-145-supl2-CR56
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- Article
Single-incision port robot-assisted surgery for thymic carcinoid tumor resection.
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- 2022
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- Publication type:
- journal article
Medullary thyroid carcinoma: surgical treatment advances.
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- Expert Review of Anticancer Therapy, 2007, v. 7, n. 6, p. 877, doi. 10.1586/14737140.7.6.877
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- Article
Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update.
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- 2013
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- journal article
The Clinical Spectrum of Multiple Endocrine Neoplasia Type 2a Caused by the Rare Intracellular RET Mutation S891A.
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- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 9, p. E92, doi. 10.1210/jc.2010-0375
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- Article
High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene.
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- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 1, p. 1318, doi. 10.1210/jc.2009-1355
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Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.
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- 2010
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- Publication type:
- journal article