review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1019164025 |
P356 | DOI | 10.1007/S00268-004-7637-4 |
P8608 | Fatcat ID | release_i777f3ixkvgv7cj4oa3yqutyci |
P698 | PubMed publication ID | 15517484 |
P50 | author | Henning Dralle | Q20752458 |
P2093 | author name string | Jörg Ukkat | |
Michael Brauckhoff | |||
Oliver Gimm | |||
Katrin Brauckhoff | |||
Carsten Sekulla | |||
Phuong Nguyen Thanh | |||
Carl-Ludwig Weiss | |||
P2860 | cites work | Early Malignant Progression of Hereditary Medullary Thyroid Cancer | Q30320549 |
Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: oncological features and biochemical properties | Q30321003 | ||
Multiple mucosal neuromata with endocrine tumours: a syndrome allied to von Recklinghausen's disease | Q34224725 | ||
Syndrome of bilateral pheochromocytoma, medullary thyroid carcinoma and multiple neuromas. A possible regulatory defect in the differentiation of chromaffin tissue | Q34225145 | ||
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression | Q34253160 | ||
Four cases of mucosal neuroma syndrome: multiple endocrine neoplasm 2B or not 2B? | Q34452953 | ||
Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid—a syndrome | Q34704956 | ||
Multiple endocrine neoplasia, type 2b | Q39781002 | ||
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis | Q40920116 | ||
Medullary thyroid carcinoma as part of a multiple endocrine neoplasia type 2B syndrome: influence of the stage on the clinical course | Q42516531 | ||
Familial medullary thyroid carcinoma and prominent corneal nerves associated with the germline V804M and V778I mutations on the same allele of RET. | Q43075498 | ||
Germline mutation of RET codon 883 in two cases of de novo MEN 2B. | Q48045271 | ||
Two germline missense mutations at codons 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation. | Q55129577 | ||
The Natural Course of Multiple Endocrine Neoplasia Type iib | Q62978399 | ||
A RET double mutation in the germline of a kindred with FMTC. | Q64992218 | ||
Medullary carcinoma of the thyroid gland | Q66908748 | ||
Prominent corneal nerves in patients with multiple endocrine neoplasia type 2A: diagnostic implications | Q67522372 | ||
No mutation at codon 918 of the RET gene in a family with multiple endocrine neoplasia type 2B | Q71336753 | ||
Multiple endocrine neoplasia type 2B: more than an endocrine disorder | Q71568258 | ||
Compartment-oriented microdissection of regional lymph nodes in medullary thyroid carcinoma | Q72116523 | ||
Update on the MEN 2A c804 RET mutation: is prophylactic thyroidectomy indicated? | Q73292314 | ||
Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation | Q73853184 | ||
Prophylactic completion thyroidectomy for differentiated thyroid carcinoma: prediction of extrathyroidal soft tissue infiltrates | Q73875550 | ||
Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918 | Q77481551 | ||
Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma | Q78121390 | ||
P433 | issue | 12 | |
P921 | main subject | multiple endocrine neoplasia | Q1553018 |
P304 | page(s) | 1305-1311 | |
P577 | publication date | 2004-11-04 | |
P1433 | published in | World Journal of Surgery | Q15763279 |
P1476 | title | Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease | |
P478 | volume | 28 |
Q42424055 | A Case of Multiple Endocrine Neoplasia Type 2B and Gangliomatosis of Gastrointestinal Tract. |
Q82589682 | Alternative surgical strategies and favorable outcomes in patients with medullary thyroid carcinoma in Japan: experience of a single institution |
Q34254131 | An introduction to managing medullary thyroid cancer |
Q38128774 | Classification and diagnostic criteria of variants of Hirschsprung's disease |
Q36355221 | Coexistence of Multiple Endocrine Neoplasia Type 2B and Chilaiditi Sign: A Case Report |
Q35082849 | Diffuse ganglioneuromatosis of intestine in a 15-year-old girl |
Q51836316 | Excellent prognosis of patients with nonhereditary medullary thyroid carcinoma with ultrasonographic findings of follicular tumor or benign nodule. |
Q47552587 | Extent of surgery for phaeochromocytomas in the genomic era. |
Q26777791 | Familial syndromes associated with neuroendocrine tumours |
Q36799232 | Genotype-phenotype based surgical concept of hereditary medullary thyroid carcinoma |
Q30317867 | German Association of Endocrine Surgeons practice guideline for the surgical management of malignant thyroid tumors |
Q37855681 | German Association of Endocrine Surgeons practice guidelines for the surgical treatment of benign thyroid disease |
Q30319384 | Hereditary thyroid cancer |
Q37921599 | Management of medullary thyroid carcinoma and MEN2 syndromes in childhood. |
Q38010030 | Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2. |
Q61795750 | Multiple Endocrine Neoplasia Type 2B |
Q33587821 | Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update |
Q34511708 | Multiple endocrine neoplasia type 2B with a RET proto-oncogene A883F mutation displays a more indolent form of medullary thyroid carcinoma compared with a RET M918T mutation |
Q38192680 | New therapeutic options for advanced forms of thyroid cancer |
Q53476597 | Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases. |
Q28480870 | Positive selection for new disease mutations in the human germline: evidence from the heritable cancer syndrome multiple endocrine neoplasia type 2B |
Q37349563 | Prognostic influence of clinical and pathological factors in medullary thyroid carcinoma: a study of 53 cases |
Q36960954 | RET signaling in endocrine tumors: delving deeper into molecular mechanisms. |
Q38510959 | RET-mediated gene expression pattern is affected by isoform but not oncogenic mutation. |
Q85020574 | Review |
Q34468665 | Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma |
Q64889815 | Static Prognostic Factors and Appropriate Surgical Designs for Patients with Medullary Thyroid Carcinoma: The Second Report from a Single-Institution Study in Japan. |
Q38614507 | Surgical Treatment of Medullary Thyroid Cancer |
Q38350561 | Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review |
Q38168128 | Timing and extent of thyroid surgery for gene carriers of hereditary C cell disease--a consensus statement of the European Society of Endocrine Surgeons (ESES). |
Q81538640 | We read with interest the article by Brauckhoff et al., in the December 2004 issue of the World Journal of Surgery |
Q39020401 | What Do We Need to Know About Colonic Polypoid Ganglioneuroma? A Case Report and A Comprehensive Review |
Q83878436 | [Genetics of endocrine tumours] |
Q83033935 | [Indication and performance of endocrine surgery. The significance of molecular genetic examination] |
Q53351755 | [Prophylactic thyroid surgery]. |
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