Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease

scientific article

Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P6179Dimensions Publication ID1019164025
P356DOI10.1007/S00268-004-7637-4
P8608Fatcat IDrelease_i777f3ixkvgv7cj4oa3yqutyci
P698PubMed publication ID15517484

P50authorHenning DralleQ20752458
P2093author name stringJörg Ukkat
Michael Brauckhoff
Oliver Gimm
Katrin Brauckhoff
Carsten Sekulla
Phuong Nguyen Thanh
Carl-Ludwig Weiss
P2860cites workEarly Malignant Progression of Hereditary Medullary Thyroid CancerQ30320549
Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: oncological features and biochemical propertiesQ30321003
Multiple mucosal neuromata with endocrine tumours: a syndrome allied to von Recklinghausen's diseaseQ34224725
Syndrome of bilateral pheochromocytoma, medullary thyroid carcinoma and multiple neuromas. A possible regulatory defect in the differentiation of chromaffin tissueQ34225145
Multiple endocrine neoplasia type 2B--genetic basis and clinical expressionQ34253160
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 syndromeQ34704956
Multiple endocrine neoplasia, type 2bQ39781002
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysisQ40920116
Medullary thyroid carcinoma as part of a multiple endocrine neoplasia type 2B syndrome: influence of the stage on the clinical courseQ42516531
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 iibQ62978399
A RET double mutation in the germline of a kindred with FMTC.Q64992218
Medullary carcinoma of the thyroid glandQ66908748
Prominent corneal nerves in patients with multiple endocrine neoplasia type 2A: diagnostic implicationsQ67522372
No mutation at codon 918 of the RET gene in a family with multiple endocrine neoplasia type 2BQ71336753
Multiple endocrine neoplasia type 2B: more than an endocrine disorderQ71568258
Compartment-oriented microdissection of regional lymph nodes in medullary thyroid carcinomaQ72116523
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 mutationQ73853184
Prophylactic completion thyroidectomy for differentiated thyroid carcinoma: prediction of extrathyroidal soft tissue infiltratesQ73875550
Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918Q77481551
Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinomaQ78121390
P433issue12
P921main subjectmultiple endocrine neoplasiaQ1553018
P304page(s)1305-1311
P577publication date2004-11-04
P1433published inWorld Journal of SurgeryQ15763279
P1476titleMultiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease
P478volume28

Reverse relations

cites work (P2860)
Q42424055A Case of Multiple Endocrine Neoplasia Type 2B and Gangliomatosis of Gastrointestinal Tract.
Q82589682Alternative surgical strategies and favorable outcomes in patients with medullary thyroid carcinoma in Japan: experience of a single institution
Q34254131An introduction to managing medullary thyroid cancer
Q38128774Classification and diagnostic criteria of variants of Hirschsprung's disease
Q36355221Coexistence of Multiple Endocrine Neoplasia Type 2B and Chilaiditi Sign: A Case Report
Q35082849Diffuse ganglioneuromatosis of intestine in a 15-year-old girl
Q51836316Excellent prognosis of patients with nonhereditary medullary thyroid carcinoma with ultrasonographic findings of follicular tumor or benign nodule.
Q47552587Extent of surgery for phaeochromocytomas in the genomic era.
Q26777791Familial syndromes associated with neuroendocrine tumours
Q36799232Genotype-phenotype based surgical concept of hereditary medullary thyroid carcinoma
Q30317867German Association of Endocrine Surgeons practice guideline for the surgical management of malignant thyroid tumors
Q37855681German Association of Endocrine Surgeons practice guidelines for the surgical treatment of benign thyroid disease
Q30319384Hereditary thyroid cancer
Q37921599Management of medullary thyroid carcinoma and MEN2 syndromes in childhood.
Q38010030Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2.
Q61795750Multiple Endocrine Neoplasia Type 2B
Q33587821Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update
Q34511708Multiple 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
Q38192680New therapeutic options for advanced forms of thyroid cancer
Q53476597Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases.
Q28480870Positive selection for new disease mutations in the human germline: evidence from the heritable cancer syndrome multiple endocrine neoplasia type 2B
Q37349563Prognostic influence of clinical and pathological factors in medullary thyroid carcinoma: a study of 53 cases
Q36960954RET signaling in endocrine tumors: delving deeper into molecular mechanisms.
Q38510959RET-mediated gene expression pattern is affected by isoform but not oncogenic mutation.
Q85020574Review
Q34468665Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma
Q64889815Static Prognostic Factors and Appropriate Surgical Designs for Patients with Medullary Thyroid Carcinoma: The Second Report from a Single-Institution Study in Japan.
Q38614507Surgical Treatment of Medullary Thyroid Cancer
Q38350561Synchronous diffuse ganglioneuromatosis and multiple schwannomas of the colon: A case report and literature review
Q38168128Timing and extent of thyroid surgery for gene carriers of hereditary C cell disease--a consensus statement of the European Society of Endocrine Surgeons (ESES).
Q81538640We read with interest the article by Brauckhoff et al., in the December 2004 issue of the World Journal of Surgery
Q39020401What 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].

Search more.